Philips Medical Systems North America OBRTBV1 Wireless Transducer User Manual ait fm manual

Philips Medical Systems North America Co. Wireless Transducer ait fm manual

Contents

User Manual

Instructions for Use Avalon Fetal MonitorFM20/30, FM40/50, Avalon CLRelease J.3. with Software Revision J.30.xxPatient Monitoring
31Table of Contents1Introduction 9Who this Book is For 9Confirm Fetal Life Before Using the Monitor 10Introducing the Avalon Family of Fetal Monitors 112What's New 29What's New in Release J.3 29What's New in Release G.0 323Basic Operation 35Supported Measurements 35Avalon FM20 and FM30 36Avalon FM40 and FM50 39Avalon CL Transducer System 40Getting to Know Your Avalon FM20/FM30 40Getting to Know Your Avalon FM40/FM50 43Transducers 45Getting to Know Your Avalon CL 47Cableless Transducers 51CL Pods 55Operating and Navigating 56Operating Modes 63Automatic Screen Layouts 64Settings 64Preparing to Monitor 67Switching the Monitor to Standby 98After Monitoring 98Disconnecting from Power 99Power On/Power Off Behavior 99Monitoring After a Power Failure 99Troubleshooting 1004FM20/30 Battery Option 101External Power Supply M8023A 102Using Batteries 102Optimizing Battery Performance 1055Alarms 109Alarm Mode 110Nurse Call Systems 110
4Visual Alarm Indicators 110Audible Alarm Indicators 111Acknowledging Alarms 114Acknowledging Disconnect INOPs 114Alarm Reminder 114Pausing or Switching Off Alarms 115Alarm Limits 117Reviewing Alarms 118Latching Alarms 118Testing Alarms 120Alarm Behavior at Power On 1216Patient Alarms and INOPs 123Alarm Messages 123Technical Alarm Messages (INOPs) 1267Admitting and Discharging 137Admit/Discharge on the Monitor 137New Patient Check 139OB TraceVue/IntelliSpace Perinatal 1398Non-Stress Test Timer 141Setting NST Autostart/Autostop 141Viewing the NST Timer 141Timer Expiry Notification 142Accessing the NST Setup Pop-up Keys 1429Non-Stress Test Report 145Setting Up an NST Report 145NST Report Status Window 146NST Criteria 148Non-Reassuring Report 149Non-Reactive NST Test 14910 Cross-Channel Verification (CCV) 151Misidentification of Heart Rates 151Cross-Channel Verification Functionality 152Overview of Cross-Channel Comparisons 152Coincidence Examples 154Recommended Actions for INOP Coincidence 15611 Monitoring FHR and FMP Using Ultrasound 157Technical Description 157Limitations of the Technology 158Misidentification of MHR as FHR 158What You Need 158
5Cableless Monitoring - Important Considerations 159Preparing to Monitor 160Selecting Fetal Heart Sound 161Changing the Fetal Heart Sound Volume 161Fetal Movement Profile 163Troubleshooting 165Additional Information 166Testing Ultrasound Transducers 17312 Monitoring Twin FHRs 175Important Considerations 175Monitoring Twins Externally 176Monitoring Twins Internally 177Separating FHR Traces 177Troubleshooting 18113 Monitoring Triple FHRs 183Important Considerations 183Monitoring Triplets 184Separating FHR Traces 184"Standard" Separation Order 184"Classic" Separation Order 185Switching Trace Separation On and Off 186When Trace Separation is On 187When Trace Separation is Off 188Troubleshooting 18814 Fetal Heart Rate Alarms 191Changing Alarm Settings 191Changing Signal Loss Delay 19215 Monitoring Uterine Activity Externally 193What You Need 193External Toco Monitoring 194Toco Sensitivity 195Troubleshooting 195Testing Toco Transducers 19516 Monitoring Uterine Activity Internally 197What You Need 197Internal (IUP) Monitoring 199Troubleshooting 19917 Monitoring FHR Using DECG 201Misidentification of MHR as FHR 201What You Need 203
6Making Connections 205Monitoring DECG 206Suppressing Artifacts 208Troubleshooting 209Testing DECG Mode 20918 Monitoring Noninvasive Blood Pressure 211Introducing the Oscillometric Noninvasive Blood Pressure Measurement 211Preparing to Measure Noninvasive Blood Pressure 212Starting and Stopping Measurements 214Enabling Automatic Mode and Setting Repetition Time 215Enabling Sequence Mode and Setting Up The Sequence 215Choosing the Alarm Source 216Assisting Venous Puncture 216Calibrating NBP 216Troubleshooting 21719 Monitoring Maternal Temperature 219Measuring Tympanic Temperature 21920 Monitoring SpO2 227Selecting an SpO2 Sensor 227Applying the Sensor 227Connecting SpO2 Cables 228Measuring SpO2 228SpO2 Signal Quality Indicator (Fast SpO2 only) 229Assessing a Suspicious SpO2 Reading 230Understanding SpO2 Alarms 230Setting Up Tone Modulation 231Setting the QRS Volume 23121 Monitoring Maternal Heart / Pulse Rate 233Priority for Maternal Heart / Pulse Rate 233Misidentification of MHR for FHR 234MHR from MECG Electrodes 235Monitoring MECG Wave 238Pulse Rate from Toco MP 240Pulse Rate from SpO2 241Adjusting the Heart Rate / Pulse Alarm Limits 241Average Pulse Rate from Noninvasive Blood Pressure 242Testing MECG Mode 242
722 Printing the ECG Waveform 24323 Paper Save Mode for Maternal Measurements 24924 Recovering Data 251Recovering Traces on Paper 251Recovering Traces on an OB TraceVue/IntelliSpace Perinatal System 252Recording Stored Data 25225 Care and Cleaning 255General Points 255Cleaning and Disinfecting 256Cleaning and Disinfecting Monitoring Accessories 257Cleaning and Disinfecting the Tympanic Temperature Accessories 258Sterilizing 25826 Maintenance 259Inspecting the Equipment and Accessories 259Inspecting the Cables and Cords 259Maintenance Task and Test Schedule 260Recorder Maintenance 260Cleaning the Print Head 265Disposing of the Monitor 26627 Accessories and Supplies 267Information on Latex 267Avalon CL Base Station 268Transducers 268Fetal Accessories 268MECG Accessories 270Noninvasive Blood Pressure Accessories 270SpO2 Accessories 273Tympanic Temperature Accessories 277Recorder Paper 277Batteries 27728 Specifications and Standards Compliance 279Environmental Specifications 279Physical Specifications 281Performance Specifications 285Recorder Specifications 294Compatible External Displays: FM40/FM50 Only 296Manufacturer's Information 296Trademark Acknowledgment 296Regulatory and Standards Compliance 297Environment 306
8Monitoring After a Loss of Power 307ESU, MRI and Defibrillation 307Cardiac Pacemakers and Electrical Stimulators 307Fast Transients/Bursts 307Symbols on the System 30829 Default Settings Appendix 311Alarm and Measurement Default Settings 311Recorder Default Settings 314Index 317
191IntroductionWho this Book is ForThis book is for trained healthcare professionals using the Avalon FM20, FM30, FM40 and FM50 Fetal/Maternal monitors, and the cableless monitoring system Avalon CL. It describes how to set up and use the monitor and transducers. Familiarize yourself with all instructions including warnings and cautions before starting to monitor patients. Read and keep the Instructions for Use that come with any accessories, as these contain important information about application and care and cleaning that is not repeated in this book.You should be:• Trained in the use of fetal heart rate (FHR) monitors.• Trained in the interpretation of FHR traces.• Familiar with using medical devices and with standard fetal monitoring procedures.For information on how to configure and service the monitor, see the Configuration Guide and the Service Guides, or contact your authorized service provider.Your monitor may not have all of the features and options described in this guide. The exact appearance of the monitor may differ slightly from that shown in the illustrations.In this guide:•A warning alerts you to a potential serious outcome, adverse event or safety hazard. Failure to observe a warning may result in death or serious injury to the user or patient.•A caution alerts you to where special care is necessary for the safe and effective use of the product. Failure to observe a caution may result in:– minor or moderate personal injury,– damage to the product or other property,– possibly in a remote risk of more serious injury.•Monitor refers to the entire fetal/maternal monitor. Display refers to the physical display unit. Screen refers to everything you see on the monitor's display, such as measurements, alarms, patient data, and so forth.FM30 • Whenever a monitor’s identifier appears to the left of a heading or paragraph, it means that the information applies to that monitor only. Where the information applies to all models, no distinction is made.
1Introduction10Avalon CTSAvalon CLWhenever one of these identifiers appear to the left of a heading or paragraph, it means that the information applies to that cableless monitoring system. Where the information applies to both systems, no distinction is made.Confirm Fetal Life Before Using the MonitorFetal monitoring technology available today is not always able to differentiate a fetal heart rate (FHR) signal source from a maternal heart rate (MHR) source in all situations. Therefore, you should confirm fetal life by independent means before starting to use the fetal monitor, for example, by palpation of fetal movement or auscultation of fetal heart sounds using a fetoscope, stethoscope, or Pinard stethoscope. If you cannot hear the fetal heart sounds, and you cannot confirm fetal movement by palpation, confirm fetal life using obstetric ultrasonography. Continue to confirm that the fetus is the signal source for the FHR during monitoring.Be aware that:• an MHR trace can exhibit features that are very similar to those of an FHR trace, even including accelerations and decelerations. Do not rely solely on trace pattern features to identify a fetal source.• Fetal Movement Profile (FMP) annotations on a fetal trace alone may not always indicate that the fetus is alive. The body of a deceased fetus can move and cause the monitor to annotate fetal body movements.Here are some examples where the MHR can be misidentified as the FHR.•When using an ultrasound transducer:– It is possible to pick up maternal signal sources, such as the aorta or other large vessels.– Misidentification may occur when the MHR is higher than normal (especially when it is over 100 bpm).•When using a fetal scalp electrode:– Electrical impulses from the maternal heart can sometimes be transmitted to the fetal monitor through a recently deceased fetus via the spiral scalp electrode cable, appearing to be a fetal signal source.– The recorded MHR (and any artifact) can be misinterpreted as an FHR (especially when it is over 100 bpm).•When Fetal Movement Profile (FMP) is enabled:FMP annotations in the absence of fetal life may be a result of:– Movement of the deceased fetus during or following maternal movement.– Movement of the deceased fetus during or following manual palpation of fetal movement (especially if the pressure applied is too forceful).– Movement of the ultrasound transducer.– The ultrasound transducer detecting a maternal movement source, such as the mother coughing.See also “Monitoring FHR and FMP Using Ultrasound” on page 155 and “Monitoring FHR Using DECG” on page 195.To reduce the possibility of mistaking the MHR for an FHR, it is recommended that you monitor both maternal and fetal heart rates. The monitor's cross-channel verification (CCV) facility can help by automatically detecting when an MHR coincides with an FHR. For further details, see “Cross-Channel Verification (CCV)” on page 149.
1 Introduction11Introducing the Avalon Family of Fetal MonitorsThe Avalon family of fetal monitors consists of the Avalon FM20, FM30, FM40 and FM50. While the FM20/FM30 and the FM40/FM50 have different form factors, the method of operation is very similar for all monitors. The Avalon fetal monitors also share transducers, accessories, software, and are compatible with the Avalon CL, and Avalon CTS Cableless Fetal Transducer Systems.Intended UseThe Philips Avalon FM20 (M2702A), FM30 (M2703A), FM40 (M2704A) and FM50 (M2705A) Fetal/Maternal Monitors are intended for:• non-invasive monitoring of fetal heart rates and movements. • non-invasive monitoring of maternal heart rates, maternal pulse rates, uterine activity, maternal noninvasive blood pressure, maternal oxygen saturation, and maternal temperature.• invasive monitoring of fetal Direct ECG and intrauterine pressure and for displaying and recording of fetal and maternal ECG waves. (FM30 and FM50 only).• displaying, storing, and recording patient data and parameter values, and for generating alarms from fetal and maternal parameters. • transmitting patient data and parameter values to a patient information and surveillance system used by trained health care professionals.• use in antepartum testing areas, in labor and delivery rooms, and during postpartum recovery in the hospital environment. They are not intended for use in intensive care units or operating rooms.• monitoring in a bath or shower. (Avalon CL cableless transducers Toco+ MP, Ultrasound, and ECG/IUP only)• transport situations in healthcare facilities, for healthcare facilities outside hospitals, such as doctors’ offices, and for use in private households. (FM20 and FM30 only)WARNINGThe fetal/maternal monitors are not intended for:• use during defibrillation, electro-surgery, or magnetic resonance imaging (MRI).• ECG measurements on patients connected to electrical stimulator or with cardiac pacemakers.• use of the invasive measurements IUP and fetal DECG, use of the patient module (M2738A) and use of the Avalon CL system in domestic establishments and those connected directly to the public low-voltage supply network that supplies buildings used for domestic purposes.WARNINGNo modification of the fetal monitors, transducers, and the Avalon CL base station is allowed.CAUTIONUS federal law restricts this device to sale by, or on the order of, a physician.
1Introduction12Connecting the Monitor to AC MainsWARNING• Always use the supplied power cord with the earthed mains plug to connect to an earthed AC mains socket. Never adapt the mains plug from the fetal monitor to fit an unearthed AC mains socket.• Check that the line frequency is correctly configured in the Global Settings menu.•FM20/FM30 only: The protective earth conductor is required for EMC purposes. It has no protective function against electric shock. Double and/or reinforced insulation protects this device against electric shock.• Do not use AC mains extension cords or multiple portable socket-outlets.Indications for UseAvalon Fetal/Maternal Monitor FM20Indicated for use by trained health care professionals whenever there is a need for monitoring of the physiological parameters uterine activity, heart rate, oxygen saturation, noninvasive blood pressure, pulse rate, and temperature of pregnant women and the fetal heart rates of single fetuses, twins, and triplets in labor and delivery rooms, in antepartum testing areas, in private households and during transports in healthcare facilities.Avalon Fetal/Maternal Monitor FM30Indicated for use by trained health care professionals whenever there is a need for monitoring of the physiological parameters uterine activity, heart rate, ECG, oxygen saturation, noninvasive blood pressure, and pulse rate and temperature of pregnant women and the fetal heart rates of single fetuses, twins, and triplets in labor and delivery rooms, in antepartum testing areas, in private households and during transports in healthcare facilities.Avalon Fetal/Maternal Monitor FM40Indicated for use by trained health care professionals whenever there is a need for monitoring of the physiological parameters uterine activity, heart rate, oxygen saturation, noninvasive blood pressure, and pulse rate and temperature of pregnant women and the fetal heart rates of single fetuses, twins, and triplets in labor and delivery rooms and in antepartum testing areas.Avalon Fetal/Maternal Monitor FM50Indicated for use by trained health care professionals whenever there is a need for monitoring of the physiological parameters uterine activity, heart rate, ECG, oxygen saturation, noninvasive blood pressure, and pulse rate and temperature of pregnant women and the fetal heart rates of single fetuses, twins, and triplets in labor and delivery rooms and in antepartum testing areas.Safety InformationIn this guide:• A warning alerts you to a potential serious outcome, adverse event or safety hazard. Failure to observe a warning may result in death or serious injury to the user or patient.• A caution alerts you to where special care is necessary for the safe and effective use of the product. Failure to observe a caution may result in minor or moderate personal injury or damage to the product or other property, and possibly in a remote risk of more serious injury.
1 Introduction13WARNINGThe fetal/maternal monitors are not intended for:• use during defibrillation, electro-surgery, or magnetic resonance imaging (MRI).• ECG measurements on patients connected to electrical stimulator or with cardiac pacemakers.• use of the invasive measurements IUP and fetal DECG, use of the patient module (M2738A) and use of the Avalon CL system in domestic establishments and those connected directly to the public low-voltage supply network that supplies buildings used for domestic purposes.WARNINGNo modification of the fetal monitors, transducers, and the Avalon CL base station is allowed.CAUTIONUS federal law restricts this device to sale by, or on the order of, a physician.WARNING• Always use the supplied power cord with the earthed mains plug to connect to an earthed AC mains socket. Never adapt the mains plug from the fetal monitor to fit an unearthed AC mains socket. • Check that the line frequency is correctly configured in the Global Settings menu.•FM20/FM30 only: The protective earth conductor is required for EMC purposes. It has no protective function against electric shock. Double and/or reinforced insulation protects this device against electric shock.• Do not use AC mains extension cords or multiple portable socket-outlets.WARNING• To avoid magnetic interference affecting the mode of the pacemaker, ensure that the Avalon CL base station does not come into close contact with implanted pacemakers.• This equipment generates, uses, and radiates radio-frequency energy, and if it is not installed and used in accordance with its accompanying documentation, may cause interference to radio communications. Operation of this equipment in a residential area may cause interference, in which case the users must take whatever measures may be required to correct the interference.
1Introduction14WARNINGDo not change the date and time setting, if the fetal monitor is connected to a Philips OB TraceVue/IntelliSpace Perinatal system via a LAN -setup. The monitor uses the OB TraceVue/IntelliSpace Perinatal system date and time, including daylight saving time changes. As long as the fetal monitor is connected to the OB TraceVue/IntelliSpace Perinatal system via the LAN-setup (locomotive icon displayed on the monitor's screen), the option to change the date and time settings at the fetal monitor are disabled, this is not valid for RS232 connections, or the connection to other systems.WARNINGShort range radio connections are subject to interruption due to interference from other radio sources in the vicinity, including microwaves, bluetooth devices, WLAN devices (802.11b,g,n) and cordless phones. Depending on the strength and duration of the interference, the interruption may occur for an extended period. A loss of connection, due to moving out-of-range, interference, or for other reasons, is indicated with a No Host Monitoring INOP (here the host is the fetal monitor) on the NBP or SpO2 Pods, or a cl NBP Disconnect or cl SpO₂ Disconnect INOP at the fetal monitor. Correct channel configuration is important, refer to the Configuration Guide for details.CAUTIONCheck the fetal monitors housing for damage before you start to monitor as part of your safety precautions.WARNINGWhen connecting devices for acquiring measurements, always position cables and NBP tubing carefully to avoid entanglement or potential strangulation.CAUTIONUsing recorder paper that is not approved by Philips can result in accelerated paper fading and can damage the thermal line printhead. This type of damage is not covered by warranty.WARNINGNever immerse the base station in liquid. You must protect it against water sprays or splashes. Place the base station where there is no chance of contact with, or falling into water or other liquids.
1 Introduction15CAUTIONAvoid the use of pulsating water jets in the bath or shower while monitoring, as these can be misinterpreted as an incorrect (or totally artificial) heart rate.Toco Baseline drift: The accuracy specified for baseline drift cannot be guaranteed for underwater usage. When using transducers under warm water the temperature increase causes a significant baseline change due to internal pressure increase. The depth under water at which the Toco transducer is used also has an effect on the Toco baseline, as the water pressure increases with depth. After immersion, allow one to two minutes for the pressure to stabilize, then adjust the Toco baseline (between contractions), and check it frequently.When using the transducers underwater, the radio transmission range is reduced, and signal loss may occur.WARNING• Always use the supplied power cord with the earthed mains plug to connect the external power supply M8023A (option #E25) to an earthed AC mains socket. Never adapt the mains plug from the power supply to fit an unearthed AC mains socket.• Do not use AC mains extension cords or multiple portable socket-outlets. If a multiple portable socket-outlet without an approved isolation transformer is used, the interruption of its protective earthing may result in enclosure leakage currents equal to the sum of the individual earth leakage currents, so exceeding allowable limits.• Do not connect any devices that are not supported as part of a system.• Any non-medical device placed and operated in the patient’s vicinity must be powered via an approved isolation transformer that ensures mechanical fixing of the power cords and covering of any unused power outlets.WARNINGDo not touch the charging contacts for the cableless transducers at the Avalon base station while you are touching the patient.)CAUTIONCondition the battery with a monitor not currently in use. The monitor switches off automatically when there is no battery power left.
1Introduction16WARNINGUse only Philips batteries part number M4605A. Use of a different battery may present a risk of fire or explosion.Do not open batteries, or dispose of them in fire, or cause them to short circuit. They may ignite, explode, leak or heat up, causing personal injury.If battery leakage should occur, avoid contact with skin. Refer to qualified and authorized service personnel.Dispose of used batteries promptly and in an environmentally-responsible manner. Do not dispose of the battery in normal waste containers. Consult your hospital administrator to find out about local arrangements. Do not expose batteries to liquids.Do not crush, drop or puncture batteries - mechanical abuse can lead to internal damage and internal short circuits which may not be visible externally.If a battery has been dropped or banged against a hard surface, whether damage is visible externally or not:• discontinue use• dispose of the battery in accordance with the disposal instructions above.Keep batteries out of the reach of children.CAUTIONDo not disassemble, heat above 100°C (212°F) or incinerate the batteries, to avoid the risk of fire and burns. Keep batteries out of the reach of children and in their original package until you are ready to use them.If battery leakage should occur, use caution in removing the battery. Avoid contact with skin. Refer to qualified and authorized service personnel.Do not install or use pre-damaged batteries.WARNINGAlarm systems of the monitor and those of the connected OB system are independent and not synchronized.WARNINGIn INOP only mode, no fetal/maternal patient alarms are enabled or indicated.
1 Introduction17WARNINGDo not rely exclusively on the audible alarm system for fetal monitoring. Adjustment of alarm volume to a low level or off during monitoring may result in a dangerous situation. Remember that the most reliable method of fetal monitoring combines close personal surveillance with correct operation of monitoring equipment.WARNINGBe aware that the monitors in your care area may each have different alarm settings, to suit different scenarios. Always check that the alarm settings are appropriate before you start monitoring.CAUTIONIn order to ensure that the settings are reset to user defaults for a new patient, always discharge the previous patient from the fetal monitor.WARNINGPerforming ultrasound imaging or Doppler flow measurements together with ultrasound fetal monitoring may cause false FHR readings, and the trace recording may deteriorate.CAUTIONNever use ultrasound transducers connected to more than one fetal monitor on the same patient.
1Introduction18WARNING• Ensure that the conductive parts of the fetal scalp electrode and the maternal leg plate electrode do not contact other conductive parts, including earth.• Indication of the heart-rate may be adversely affected by the operation of cardiac pacemaker pulses or by cardiac arrhythmias.• During ambulant FHR monitoring, the chance of losing the signal or detecting the maternal heart rate is higher than during stationary monitoring. The frequency of the patient's walk may be detected, and mistaken for a FHR signal.• Check the mother’s pulse periodically during monitoring and compare this with the FHR signal. Beware of mistaking a “doubled” maternal heart rate for FHR. In the case of a dead fetus, there is a risk that the maternal heart rate is monitored and misinterpreted as the fetal heart rate. Therefore, the simultaneous monitoring of maternal heart rate (preferably, the maternal ECG) is encouraged.• Do not interpret maternal movements as fetal movements.• Artifacts: FMP artifacts are generated during fetal heart rate searching by changing the transducer position, therefore Philips fetal monitors enable the FMP only after detecting a valid heart rate signal for several seconds. FMP is not recommended when the mother is likely to move, and you should disable Fetal Movement Profile (FMP) at the fetal monitor (FMP Off) if the mother is walking.• Gaps and maternal heart rate detection can occur:– if the transducer is not correctly positioned.– due to the pulsation of uterine blood vessels.–if the fetus moves.CAUTIONUsing ultrasound gel not approved by Philips may reduce signal quality and may damage the transducer. This type of damage is not covered by warranty.WARNINGPeriodically compare the mother's pulse with the signal coming from the monitor's loudspeaker to ensure that you are monitoring fetal heart rate. Do not mistake a doubled or elevated MHR for FHR.WARNINGDo not catheterize if placenta previa is diagnosed, or if uterine bleeding from an undetermined source is present.
1 Introduction19WARNINGNever attempt to connect the fetal scalp electrode to anything other than the correct DECG adapter cable.WARNINGThe fetal/maternal monitor is not a diagnostic ECG device. In particular, the display of fetal/maternal ECG is intended only for evaluating signal quality for fetal/maternal heart rate as derived from the ECG waveform.When in doubt, it can be used to identify sources of compromised signal quality, such as noise or muscle artifacts. It can subsequently be used to verify the result of measures taken to resolve them (e.g. checking ECG cable connections or adapting the fetal ArtifactSuppress configuration).The safety and effectiveness of the displayed fetal/maternal ECG waveform (i.e. P, QRS and T segments) for evaluation of fetal/maternal cardiac status during labor have not been evaluated.WARNINGIntravenous infusion: Do not use the NBP cuff on a limb with an intravenous infusion or arterial catheter in place. This could cause tissue damage around the catheter when the infusion is slowed or blocked during cuff inflation.Skin Damage: Do not measure NBP in cases of sickle-cell disease or any condition where skin damage has occurred or is expected.Unattended measurement: Use clinical judgment to decide whether to perform frequent unattended blood pressure measurements in cases of severe blood clotting disorders because of the risk of hematoma in the limb fitted with the cuff.WARNINGDo not use the thermometer in the presence of flammable anesthetics, such as a flammable anesthetic mixture with air, oxygen or nitrous oxide.
1Introduction20WARNING• Never apply the probe to the patient when the probe is not connected to the unit.• Always use a single-use probe cover to limit patient cross-contamination.• Measurement errors or inaccurate readings may result when:– probe covers other than the specified probe covers are used (see “Tympanic Temperature Accessories” on page 267)• Insert the probe slowly and carefully to avoid damage to the ear canal and the tympanic membrane.• Inspect the probe for damage, holes, tears, or sharp edges to avoid injuring the skin.• Always ensure that the used probe cover is removed before attaching a new probe cover.CAUTION• Do not immerse the probe in fluids, or drop fluids on the probe.• Do not use a probe cover that has been dropped or is damaged.• Do not autoclave. To prevent damage to the unit, probe and accessories, refer to the cleaning procedures in the “Cleaning and Disinfecting” on page 246 chapter.CAUTIONDo not use OxiCliq disposable sensors in a high humidity environment, or in the presence of fluids, which may contaminate sensor and electrical connections causing unreliable or intermittent measurements. Do not use disposable sensors when there is a known allergic reaction to the adhesive.WARNINGProper Sensor Fit: If a sensor is too loose, it might compromise the optical alignment or fall off. If it is too tight, for example because the application site is too large or becomes too large due to edema, excessive pressure may be applied. This can result in venous congestion distal from the application site, leading to interstitial edema, hypoxemia and tissue malnutrition. Skin irritations or lacerations may occur as a result of the sensor being attached to one location for too long. To avoid skin irritations and lacerations, periodically inspect the sensor application site and change the application site regularly.Venous Pulsation: Do not apply sensor too tightly as this results in venous pulsation which may severely obstruct circulation and lead to inaccurate measurements.Ambient Temperature: At elevated ambient temperatures be careful with measurement sites that are not well perfused, because this can cause severe burns after prolonged application. All listed sensors operate without risk of exceeding 41°C on the skin if the initial skin temperature does not exceed 35°C.Extremities to Avoid: Avoid placing the sensor on extremities with an arterial catheter, an NBP cuff or an intravascular venous infusion line.
1 Introduction21WARNING• For fully conscious pediatric or adult patients, who have a normal function of perfusion and sensory perception at the measurement site:To ensure skin quality and correct optical alignment of the sensor, inspect the application site when the measurement results are suspicious or when the patient complains about pressure at the application site, but at least every 24 hours. Correct the sensor alignment if necessary. Move the sensor to another site, if the skin quality changes.• For all other patients:Inspect the application site every two to three hours to ensure skin quality and correct optical alignment. Correct the sensor alignment if necessary. If the skin quality changes, move the sensor to another site. Change the application site at least every four hours.• Injected dyes such as methylene blue, or intravascular dyshemoglobins such as methemoglobin and carboxyhemoglobin may lead to inaccurate measurements.• Inaccurate measurements may result when the application site for the sensor is deeply pigmented or deeply colored, for example, with nail polish, artificial nails, dye or pigmented cream.• Interference can be caused by:– High levels of ambient light (including IR warmers) or strobe lights or flashing lights (such as fire alarm lamps). (Hint: cover application site with opaque material.)– Another SpO2 sensor in close proximity (e.g. when more than one SpO2 measurement is performed on the same patient). Always cover both sensors with opaque material to reduce cross-interference.– Electromagnetic interference, especially at perfusion indicator values below 1.0 or signal quality indicator below medium.– Excessive patient movement and vibration.WARNINGWith pulse oximetry, sensor movement, ambient light (especially strobe lights or flashing lights) or electromagnetic interference can give unexpected intermittent readings when the sensor is not attached. Especially bandage-type sensor designs are sensitive to minimal sensor movement that might occur when the sensor is dangling.CAUTIONIf you measure SpO2 on a limb that has an inflated noninvasive blood pressure cuff, a non-pulsatile SpO2 INOP can occur. If the fetal monitor is configured to suppress this alarm there may be a delay of up to 60 seconds in indicating a critical status, such as sudden pulse loss or hypoxia.
1Introduction22WARNINGThe fetal/maternal monitor is not a diagnostic ECG device. In particular, the display of fetal/maternal ECG is intended only for evaluating signal quality for fetal/maternal heart rate as derived from the ECG waveform.When in doubt, it can be used to identify sources of compromised signal quality, such as noise or muscle artifacts. It can subsequently be used to verify the result of measures taken to resolve them (e.g., checking ECG cable connections).The safety and effectiveness of the displayed fetal/maternal ECG waveform (i.e., P, QRS and T segments) for evaluation of fetal/maternal cardiac status during labor have not been evaluated.WARNINGThe fetal/maternal monitor is NOT intended for use during defibrillation, electro-surgery, or MRI. Remove all transducers, sensors, and accessories before performing electro-surgery, defibrillation, or MRI, otherwise harm to the patient or the user can result.WARNING• No alarm is possible when Toco MP or CL Toco+MP transducer is the source of the pulse rate.• No QRS tone is audible when Toco MP or CL Toco+MP transducer is the source of the pulse rate.• The Toco MP or CL Toco+MP transducer signal is significantly less reliable if the patient is up and moving about, or is pushing during the second stage of labor.WARNINGNo alarm is possible when noninvasive blood pressure is the source of the pulse rate.CAUTIONOnly use Philips paper. Using paper other than Philips paper may result in the failure to recover traces.CAUTIONEnsure that you admit each patient by name, including other patient identification information, and discharge the patient when you have finished monitoring, so that you can identify which trace period (entry in the patient list) refers to which patient.
1 Introduction23WARNING• Do not operate the monitor if it is wet. If you spill liquid on the monitor, contact your service personnel or Philips service engineer.• Do not perform underwater monitoring (for example, in a bath or shower) using wired transducers.• Place the monitor where there is no chance of contact with, or falling into water or other liquid.• Do not dry equipment using heating devices such as heaters, ovens (including microwave ovens), hair dryers and heating lamps.• Do not put equipment or accessories in autoclave (for sterilization).CAUTIONSolutions: Do not mix disinfecting solutions (such as bleach and ammonia) as hazardous gasses may result.Skin contact: To reduce the risk of skin irritations, do not allow a cleaning or disinfecting agent to leave residues on any of the equipment surfaces - wipe it off with a cloth dampened with water, after allowing the appropriate time for the agent to work, or before applying to a patient.Hospital policy: Disinfect the product as determined by your hospital's policy, to avoid long term damage to the product.Local requirements: Observe local laws governing the use of disinfecting agents.Touch display: To clean and disinfect the touch-enabled display, disable the touch operation by switching off the monitor during the cleaning procedure, or by selecting and holding the Main Screen key until the padlock symbol appears on it, indicating that touch operation is disabled. Select and hold again to re-enable touch operation.WARNINGDo not put device and accessories in autoclave (for sterilization).WARNINGSchedule: Failure on the part of the responsible individual hospital or institution employing the use of this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards.In case of problems: If you discover a problem with any of the equipment, contact your service personnel, Philips, or your authorized supplier.Electric shock hazard: Do not open the monitor housing. Refer all servicing to qualified service personnel.
1Introduction24WARNINGTo avoid contaminating or infecting personnel, the environment or other equipment, make sure you disinfect and decontaminate the monitor appropriately before disposing of it in accordance with your country's laws for equipment containing electrical and electronic parts. For disposal of parts and accessories such as thermometers, where not otherwise specified, follow local regulations regarding disposal of hospital waste.WARNINGReuse: Disposable accessories and supplies intended for single use, or single use only, and are indicated as such on their packaging. Never reuse disposable accessories and supplies, such as transducers, sensors, electrodes and so forth that are intended for single use, or single patient use only.Approved accessories: Use only Philips-approved accessories.Packaging: Do not use a sterilized accessory if its packaging is damaged.Protection against electric shocks: The transducers and accessories listed in this chapter are not defibrillator proof.Electro-Surgery, Defibrillation and MRI: The fetal/maternal monitors are not intended for use during defibrillation, electro-surgery, or MRI. Remove all transducers, sensors, and accessories before performing electro-surgery, defibrillation, or MRI, otherwise harm can result.WARNINGExplosion Hazard: Do not use in the presence of flammable anesthetics, such as a flammable anesthetic mixture with air, oxygen, nitrous oxide, or in oxygen rich environment. Use of the devices in such an environment may present an explosion hazard.WARNING• Do not use additional AC mains extension cords or multiple portable socket-outlets. If a multiple portable socket-outlet is used, the resulting system must be compliant with IEC/EN 60601-1 A1: 2012.• Do not connect any devices that are not supported as part of a system.• Do not use a device in the patient vicinity if it does not comply with IEC/EN 60601-1 A1: 2012. The whole installation, including devices outside of the patient vicinity, must comply with IEC/EN 60601-1 A1: 2012. Any non-medical device, including a PC running an OB TraceVue system, placed and operated in the patient's vicinity must be powered via a separating transformer (compliant with IEC/EN 60601-1 A1: 2012) that ensures mechanical fixing of the power cords and covering of any unused power outlets.• Do not use USB devices with own power supplies unless an appropriate separation device is used (either between USB interface and device or between device and power).
1 Introduction25CAUTION•FM20/FM30 only: Although this is an electrical Class II device, it has a protective earth conductor which is needed for EMC purposes.• Always use the supplied power cord with the three-prong plug to connect the monitor to AC mains. Never adapt the three-prong plug from the power supply to fit a two-slot outlet.CAUTIONThe use of accessories, transducers and cables other than those specified may result in increased electromagnetic emissions or decreased electromagnetic immunity of the device.WARNINGDo not use cordless/mobile phones or any other portable RF communication system within the patient vicinity, or within a 1.0 m radius of any part of the fetal monitoring system.WARNINGFor paced patients: The radiated SRR power of the CL SpO2 and NBP Maternal Cableless Measurement Devices, the CL Transmitter, and other sources of radio-frequency energy, when used in very close proximity of a pacemaker, might be sufficient to interfere with pacemaker performance. Due to shielding effects of the body, internal pacemakers are somewhat less vulnerable than external pacemakers. However, caution should be exercised when monitoring paced patients.In order to minimize the possibility of interference, avoid positioning and wearing the Cableless Measurement Devices in very close proximity to a pacemaker. Consult the pacemaker manufacturer for information on the RF susceptibility of their productsCAUTIONFetal parameters, especially ultrasound and ECG, are sensitive measurements involving small signals, and the monitoring equipment contains very sensitive high gain front-end amplifiers. Immunity levels for radiated RF electromagnetic fields and conducted disturbances induced by RF fields are subject to technological limitations. To ensure that external electromagnetic fields do not cause erroneous measurements, it is recommended to avoid the use of electrically radiating equipment in close proximity to these measurements.CAUTIONThe device should not be used adjacent to, or stacked with, other equipment unless otherwise specified.
1Introduction26WARNING•Leakage currents: If several items of equipment used to monitor a patient are interconnected, the resulting leakage current may exceed allowable limits.•ECG electrodes: NEVER allow ECG electrodes to contact other electrical conductive parts, including earth.WARNINGThe fetal/maternal monitors are NOT intended for use during defibrillation, electro-surgery, or MRI. Remove all transducers, sensors, and accessories before performing electro-surgery, defibrillation, or MRI, otherwise harm to the patient or the user can result.WARNINGThe fetal/maternal monitors are not intended for use for ECG measurements on patients connected to external electrical stimulator or with cardiac pacemakers.
127Device Classification and Names within this ManualNew cableless measurements for fetal and maternal monitoring supplement the Avalon fetal monitor family. The Avalon CL solution consists of the Avalon CL base station, the Avalon CL transducers, and the IntelliVue CL Pods. The IntelliVue CL Pods are only used for maternal measurements within the Avalon CL solution. To differentiate between the CL transducers and the CL Pods, the CL Pod are also referred to as maternal measurement Pods. The following table provides an overview of all the devices within the solution.Avalon FM20/FM30 and FM40/FM50Wired TransducersAvalon CL Base Station Avalon CL TransducersIntelliVue CL PodsFM20/FM30M2702A and M2703AFM40/FM50M2704A and M2705AAvalon CL Base Station866074US transducerwiredM2736AAvalon CL Toco+ MP Transducercableless866075IntelliVue CL NBP Podcableless865216
1Introduction28Toco/ Toco MP transducerwiredM2734A and M2734BAvalon CL US Transducercableless866076IntelliVue CL SpO2 Podcableless865215Toco+ transducer with ECG/IUP capabilitywiredM2735AAvalon CL ECG/IUP Transducercableless866077Patient Module for ECG/IUPM2738AAvalon FM20/FM30 and FM40/FM50Wired TransducersAvalon CL Base Station Avalon CL TransducersIntelliVue CL Pods
2What's New292What's NewThis section lists the most important new features and improvements to the fetal monitors and their user interface introduced with Release J.3. You may not have all of these features, depending on the fetal monitor configuration purchased.What's New in Release J.3Avalon CL Transducer SystemThe Avalon CL system provides cableless monitoring with the Avalon FM20/FM30 and FM40/FM50 with the same functionality and performance as the wired measurement devices (e.g. twin and triplets monitoring). The Avalon CL has a straight-forward handling and operating concept. The cableless transducers are assigned by simply docking them at the base station, no further configurations are necessary.The Avalon CL system includes the following features:• Cableless monitoring of twins and triplets• Cableless maternal measurement Pods CL SpO2 and CL NBP• Maternal pulse from a CL Toco+MP (Smart Pulse) transducer• A cableless ECG/IUP transducer measuring IUP and fetal/maternal ECG• Watertight cableless transducers that can be used to monitor in water• Patient call that pages an ambulating mother with an audible signal emitted by the worn CL transducers.• Out of range audible signal emitted by the worn CL transducers to inform an ambulating mother that she is approaching the limit of the active signal area of reach.• A transducer finder LED on all cableless transducers to help identify the assigned transducerSupport For Use of Maternal Cableless Measurement DevicesThe IntelliVue measurement pods are patient-worn, battery powered measurement devices for SpO2 and NBP. The devices provide measurement values on the built-in display and communicate them to the fetal monitor using the wireless short range radio (SRR) interface of the Avalon CL base station.Maternal Temperature MeasurementTo measure maternal temperature, the new optional Tympanic Temperature device (866149) is available for the Avalon fetal monitors. The measurement data is:• fully documented at the local recorder and the OB system,• can be displayed as a numeric on the screen,• and is printed out on the recorder trace strip.
2What's New30Manually Entered Maternal Temperature MeasurementsManually measured temperatures can be entered manually into the fetal monitor and stored in the database. They are also displayed as a numeric on screen, and are printed out on the recorder trace if required.New Design for the User InterfaceThe user interface for the fetal monitors has been redesigned to bring the presented information into the foreground, letting the structural elements such as keys and frames retreat into the background. Additionally special regard was given to making the "look and feel" similar to that of standard software products.New SmartKeys•The Start ECG SmartKey is renamed to Record ECG .•With the Call Patient SmartKey you can now page patients who are ambulating wearing cableless transducers.•With the Tele Info SmartKey you can call up the Tele Info window on the fetal monitor display. In the Tele Info window you can control and view the status of the cableless transducers from the connected Avalon CL system. •With the Enter Temp SmartKey a pop-up window opens showing a numeric pad for entering externally measured maternal temperature values.Coincidence INOP ToneWhen the cross-channel verification detects that the signal of the maternal heart rate coincides with the fetal heart rate, the Coincidence INOP is issued with a tone at the fetal monitor. The Coincidence INOP tone has a configurable delay. Increased Internal Back-up MemoryThe internal back-up memory is now able to store data at least 3 hours.USB InterfaceAn optional USB interface allows the use of USB printers, bar code readers, and input devices such as a keyboard or mouse.Flexible Nurse Call InterfaceAn optional Flexible Nurse Call interface allows now the connection of a nurse call device to the fetal monitors.DHCP SupportThe DHCP support offers an alternative to BOOTP. DHCP (dynamic host configuration protocol) enables the fetal monitors to request an IP address (internet protocol address) from the connected network (OB TraceVue/IntelliSpace Perinatal) automatically.
2What's New31Data Export SupportYou can now export measurement values from the monitor to other devices via the LAN or RS232 interface.NBP Configurable Measurement SequenceUp to four measurement cycles can be set up which will run consecutively. For each cycle you can set the number of measurements and the interval between them. By setting the last cycle to run continuously you can have regular measurements continue after the sequence has run.Alarms Enhancements• In addition to the standard blue INOPs, some INOPs can now be configured as red or yellow INOPs to provide a severity indication (ECG Leads Off, NBP Cuff Overpress, Cuff Not Deflated). A small number of INOPs are always yellow or red to indicate a severity corresponding to red and yellow alarms.• For the invasive pressure measurement, the extreme pressure alarms Extreme High and Extreme Low can be made available for your monitor in Configuration Mode and are additional to the standard High and Low limit alarms.•The Review Alarms window now shows when the monitor was switched on (after being switched off for longer than 1 minute) and any changes made to the Standby and paired status.• In order to improve alarming on asystole under certain conditions, you can set Asystole Detect. in Configuration Mode to Enhanced. In enhanced mode an asystole alarm will be suppressed for up to five seconds if a valid beat-to-beat Pulse is detected from a Pressure.Alarm ReminderIn Configuration Mode you can set now an Alarm Reminder. The Alarm Reminder emits an audible reminder of alarm conditions that remain active after the alarm is acknowledged. This reminder may take the form of a repetition of the alarm tone for a limited time, or an unlimited repetition of the alarm tone (this is the same as a new alarm). The interval between silencing the alarm and sounding the reminder tone can be set to one, two, or three minutes. Auto FreeIn Configuration Mode you can now set an Auto Free setting which discharges a patient automatically when the fetal monitor is powered off, or is in standby mode for a set time. Only the demographic patient data is deleted, the trace data is not affected. What's New in Release G.0Battery Option and Patient Transport Improvements for the Avalon FM20 and FM30• For the FM20/FM30, you can now switch between battery-powered and mains-powered operation without interrupting monitoring. The monitor is connected to the AC mains power with the external power supply.• Traces of multiple patients can be recorded during transport and can automatically be uploaded to OB TraceVue/IntelliSpace Perinatal (Rev. G or higher) when reconnected.
2What's New32• A bed hanger is available as a mounting option, especially for patient transport purposes within healthcare facilities.Maternal Pulse from Toco MP Transducer• The new Toco MP transducer can measure the maternal pulse rate, in addition to the other available sources; MECG, SpO2, and NBP. With sensors built-into the bottom cover of the Toco MP transducer, and using a measurement technology similar to SpO2, it automatically gives you an additional maternal pulse source for Cross-Channel Verification (CCV).• The new Toco MP transducer is standard for the whole product family, Avalon FM20 to FM50.Non Stress Test (NST) Analysis as Clinical Decision Support (CDS) Application• The optional NST Report Trace Interpretation feature allows you to automatically interpret FHR traces and to generate a printed NST report, equivalent to the NST report functionality in OB TraceVue Rev. F and based on the NICHD guidelines from 1997.• The application can be adapted to domestic or hospital guidelines. A report of the NST analysis can be printed automatically or on demand.• This software option is available for the whole product family, Avalon FM20 to FM50.FHR Sound SourceA newly-connected fetal measurement (FHR or DFHR) automatically becomes the FHR sound source, without the need for manual intervention. If you prefer the previous behavior, this can be changed in Configuration mode (Audio Select setting).FHR Numeric DisplayThe FHR numeric display shows changes in fetal heart rate faster and is updated more frequently.Improved FHR and DFHR Label ConceptA DFHR numeric (fetal heart rate from DECG measurement) now also has a unique number (DFHR1, DFHR2, or DFHR3) to allow easier identification of the related trace in OB TraceVue/IntelliSpace Perinatal.New SmartKeysYou can control fetal heart sound volume directly with the configurable SmartKeys (FHR Vol. Up and FHR Vol.Down) on the monitor’s screen.Now the Toco Baseline SmartKey automatically turns into the Zero IUP SmartKey when switching to IUP measurement.Trace Separation On/Off OperationNow you can switch the Trace Separation on or off in every FHR setup menu.NBP• To prevent the NBP measurement from being switched on or off accidentally, this operation is now only available in Configuration Mode.
233• You can enter the NBP setup menu by touching the NBP numeric (on the screen) before the first measurement is taken.• Algorithm enhancements (more tolerant of movement artifacts).Alarms• There is an individual Alarm Tone Volume setting for Yellow, Red and Cyan alarms.• The new alarm settings available in Configuration Mode are:–AutoIncrease Vol and IncreaseVolDelay–AlarmsOffAtStart–ConfirmAlarmsOffFor a detailed description of the settings see the Configuration Guide.CCV INOPThere is a new INOP (technical alarm) Coincidence after 1 minute of persistent coincidence warning.New Demographic Fields•Date of Birth and Gestational Age can be entered for complete documentation in an NST Report (supporting the optional NST Trace Interpretation software feature).•A Middle Name field is now available in the admission form - whether it appears is configurable.• Two additional ID fields Lifetime ID and Encounter ID can also be configured to appear, and their names can be customized to fit hospital requirements. The default label of the Lifetime ID is MRN.Recorder• It can now be configured whether the recorder speed can only be adjusted in Configuration mode, or also in Monitoring mode.• When recorder speed is changed, a new trace header is printed. Date and/or time changes are annotated in real time recording.Stored Data RecordingPrinting progress is shown while printing a trace from the internal back-up memory.FHR Sound VolumeVolume steps are optimized in the low range to allow finer FHR sound volume adjustments.Avalon CTSAn antenna symbol is displayed next to MECG waves if an Avalon CTS is used.
2What's New34
3 Basic Operation353Basic OperationThis chapter gives you an overview of the monitor and its functions. It tells you how to perform tasks that are common to all measurements (such as entering data, switching a measurement on, changing some monitor settings, and setting up the recorder). The alarms section gives an overview of alarms. The remaining sections tell you how to perform individual measurements, and how to care for and maintain the equipment.Supported MeasurementsThe following Fetal measurements are supported:Fetal Monitor or ModelFetal Heart Rate (FHR) via US (including Twins) Triple FHR via US TocoFHR via Direct ECG (DECG)Intrauterine Pressure (IUP)FM20Standard Optional Standard - -Optional Optional Standard - -FM30Standard Optional Standard Standard StandardOptional Optional) Standard Standard StandardFM40Standard Optional Standard - -Optional Optional Standard - -FM50Standard Optional Standard Standard StandardOptional Optional Standard Standard Standard
3 Basic Operation36The following Maternal measurements are supported:Avalon FM20 and FM30This section outlines the capabilities of your monitor.Fetal Monitor or ModelMaternal Heart Rate (MHR) via Maternal ECG ElectrodesMaternal ECG (MECG) WaveMaternal Pulse from TocoNon-invasive Blood Pressure with Pulse RatePulse Oximetry (Maternal SpO2) with Pulse RateMaternal TemperatureFM20Standard -Standard Optional (built-in) -Optional (Interface cable and manual entry)Standard -Standard Optional (cableless)Optional (cableless)-FM30Standard Standard Standard Optional (built-in) Optional (built-in) Optional (Interface cable and manual entry)Standard Standard Standard Optional (cableless)Optional (cableless)-FM40Standard -Standard Standard (built-in) Standard (built-in) Optional (Interface cable and manual entry)Standard -Standard Optional (cableless)Optional (cableless)-FM50Standard Standard Standard Standard (built-in) Standard (built-in) Optional (Interface cable and manual entry)Standard Standard Standard Optional (cableless)Optional (cableless) -
3 Basic Operation37Avalon FM20The Avalon FM20 fetal/maternal monitor provides a solution for external fetal monitoring applications, and optional noninvasive maternal vital signs.You can monitor fetal heart rates (FHRs) externally using ultrasound, uterine activity and maternal pulse using an external Toco transducer, and the maternal heart rate (MHR) with maternal ECG electrodes, and optionally, noninvasive blood pressure and maternal oxygen saturation (SpO2).Measurements are displayed on a 6.5-inch color display as numerics. The display is a touchscreen, and you operate the monitor using this touchscreen interface. The integrated recorder documents fetal and maternal measurements as well as the user-defined annotations.You can connect the monitor to an OB TraceVue/IntelliSpace Perinatal system via the RS232 connection, or over a LAN connection (with OB TraceVue Revision E.00.00 and later, or IntelliSpace Perinatal Revision H.0 and later).Avalon FM30The Avalon FM30 fetal/maternal monitor offers a solution for both external and internal fetal monitoring applications, and optional noninvasive maternal vital signs.The Avalon FM30 shares all the features and capabilities of the Avalon FM20. In addition, you can monitor one FHR internally with a direct fetal electrocardiogram (DECG), uterine activity internally using an intra-uterine pressure (IUP) catheter together with a Toco+ transducer or patient module.The Avalon FM30 carries the IP label, indicating that it is capable of intrapartum monitoring.FM20/30withBatteryOption#E25 OnlyThe battery option for the FM20/30 provides support for the in-transport monitoring of all measurements when disconnected from a power supply. Existing data storage is automatically uploaded to OB TraceVue or IntelliSpace Perinatal after reconnecting it to the system. Trace printing during transport is also possible.
3 Basic Operation38Avalon FM40 and FM50This section outlines the capabilities of your monitor.Avalon FM40The Avalon FM40 fetal/maternal monitor provides a solution for external fetal monitoring applications, and noninvasive maternal vital signs.You can monitor fetal heart rates (FHRs) externally using ultrasound, uterine activity using an external Toco transducer, and the maternal heart rate (MHR) via maternal ECG electrodes, and non-invasive blood pressure and maternal oxygen saturation (SpO2).Measurements are displayed on a 6.5-inch color display as numerics. The display is a touchscreen, and you operate the monitor using this touchscreen interface. The integrated recorder documents fetal and maternal measurements as well as the user-defined annotations.You can connect the monitor to an OB TraceVue/IntelliSpace Perinatal system with the RS232 connection, or over a LAN connection (with OB TraceVue Revision E.00.00 and later, or IntelliSpace Perinatal Revision H.0 and later).Avalon FM50The Avalon FM50 fetal/maternal monitor offers a solution for both external and internal fetal monitoring applications, and noninvasive maternal vital signs.The Avalon FM50 shares all the features and capabilities of the Avalon FM40. In addition, you can monitor one FHR internally with a direct fetal electrocardiogram (DECG), and uterine activity internally using an intra-uterine pressure (IUP) catheter together with a Toco+ transducer or patient module.The Avalon FM50 carries the IP label, indicating that it is capable of intrapartum monitoring.
3 Basic Operation39Avalon CL Transducer SystemThe Avalon CL Fetal Transducer System lets you monitor the patient continuously with cableless transducers during the antepartum period, labor, and delivery. You can monitor the fetal heart rate (FHR) using noninvasive CL Ultrasound transducers, or invasively using the CL ECG/IUP transducer with the direct electrocardiogram (DECG). The uterine activity can be monitored using an external CL Toco+ MP transducer. The fetal and maternal parameters are measured and transmitted via radio frequency from the CL transducers to the CL base station, eliminating the need for patient cables. With the Avalon CL Transducer System you can monitor a single fetus, twins and triplets.The Avalon fetal monitor (FM20-FM50) connected to the CL base station displays and records the parameters. All the CL transducers are watertight. You can continuously monitor patients in a bath or shower using the CL Toco+MP and the CL Ultrasound transducers.The system should only be used by, or under the direct supervision of, a licensed physician or other health care practitioner, who is trained in the use of FHR monitors and in the interpretation of FHR traces.Getting to Know Your Avalon FM20/FM30Overview1Touchscreen Display (tilt and fold)2Power LED3Paper Drawer4Paper Drawer release5Connectors
3 Basic Operation40Right SidewithBatteryOptionLeft SideEach of the fetal sensor sockets accepts any fetal transducer, one Avalon CL or one Avalon CTS Cableless Fetal Transducer System base station, or an event marker.1On/Off Switch2Power Connector1On/Standby Switch2MSL Connector1SpO2 Socket (optional)2Noninvasive Blood Pressure Socket (optional)3Fetal Sensor Sockets
3 Basic Operation41BottomThere are five optional interfaces available for the Avalon FM20/30 monitor:• LAN/RS232 system interface• Dual PS/2 interface• MIB/RS232 interface• Flexible Nurse Call • USB portYou can use two of the five optional interfaces at the same time.1LAN/RS232 system interface2Dual PS/2 system interfaceOptional Interfaces DescriptionFlexible nurse call interface cardUSB ports
3 Basic Operation42RearGetting to Know Your Avalon FM40/FM50FrontConnect any fetal sensor or patient module at the fetal sensor sockets, including an Avalon CL or an Avalon CTS via interface cable (with red connector).1Display Release2Carrying Handle3Built-in Stand1Touchscreen color display2Transparent paper guide with tear-off edge3Paper eject button4Power LED5On/Standby switch6Recorder paper table7Fetal sensor sockets8Noninvasive blood pressure socket9SpO2 socket
3 Basic Operation43RearTwo Avalon CL, or one Avalon CTS can be also connected to the Telemetry interface sockets using the interface cable (with black connector).Additional Optional Interfaces1Reserved for future use: protective earth intended for use in system installations.2Equipotential grounding point3Power cord connector4Loudspeaker5Slot 01 for optional LAN/RS232 system interface (for connection to an obstetrical information and surveillance system)6Slot 03 reserved for future use7Video output (VGA)8Telemetry interface9Slot 02 for optional interfaces: Either dual PS/2 system interface (A) for mouse and keyboard connection) Or MIB interface (B) for external touch screen connection.Optional Interfaces DescriptionFlexible nurse call interface cardUSB ports
3 Basic Operation44TransducersToco (M2734A) and Toco MP Transducer (M2734B)1Transducer finder LED - lights up on the transducer providing the measurement source2"MP" for M2734B "Toco MP" transducers (additionally capable of providing the maternal pulse measurement)3Belt ButtonUltrasound Transducer (M2736A)1Cable - connects to any of the four fetal sensor sockets on the monitorThe M2736AA US transducer is identical to the M2736A US transducer, including all specifications Toco+ Transducer with ECG/IUP capability (M2735A)1Connector - for connecting ECG/IUP adapter cables (M2735A Toco+ transducer only)
3 Basic Operation451Butterfly belt clip (shown fitted; for use with belts without button holes)2Close-up of MECG adapter cable connected to Toco+ transducer3Close-up of active finder LEDPatient Module for ECG/IUP (M2738A)1Connector - for connecting ECG/IUP adapter cables (same as for Toco+ transducer)2Cable - connects to any of the four fetal sensor sockets on the monitor
3 Basic Operation46Getting to Know Your Avalon CLFrontWARNING• To avoid magnetic interference affecting the mode of the pacemaker, ensure that the Avalon CL base station does not come into close contact with implanted pacemakers.• This equipment generates, uses, and radiates radio-frequency energy, and if it is not installed and used in accordance with its accompanying documentation, may cause interference to radio communications. Operation of this equipment in a residential area may cause interference, in which case the users must take whatever measures may be required to correct the interference.1Transducer docking slots2On/Standby button with power LED3Device label4LED for optional cableless pods5Docking slots for cableless pods
3 Basic Operation47Docking Slot for Cableless TransducersThe Avalon CL base station has three docking slots to mechanically hold the CL transducers. The flexible electronic contacts identify the transducer type after docking. The transducers are charged while docked. The base station has a built-in radio interface with an integrated antenna to communicate with the transducers for assignment, configuration, and for transducer firmware updates. The transducers can be controlled with the base station and the fetal monitor.On/Standby ButtonPressing the On/Standby button switches the Avalon CL base station between the two modes On and Standby.If you switch the base station to On, the LED button lights up green. The base station is ready for use. The CL transducers are charging. When the transducers are picked up from their docking slot, the base station sets up the radio communication to the CL transducer automatically. Wired transducers connected to the fetal monitor are disabled, and the antenna symbol for the CL transducer is displayed on the screen of the fetal monitor. If you switch the base station to Standby, the LED button turns off. The base station is now in Standby mode. The docked CL transducers continue charging. No radio communication occurs, any existing radio communication is stopped.If the LED of the On/Standby button turns red, it indicates a technical problem has occurred that needs your attention. Check your monitor for a possible related INOP message.1On/Standby button
3 Basic Operation48Docking Slots for Cableless Measurement PodsThe Avalon CL base station has one docking slot to mechanically hold an IntelliVue CL pod. The electronic contacts identify the CL pod type after docking. The CL pod is charged while docked. The LED under the docking slot indicates the battery status of the CL pod. The base station has a built-in short range radio interface with an integrated antenna to communicate with the CL pod for assignment and configuration. The CL pod can be controlled with the base station and the fetal monitor.WARNINGShort range radio connections are subject to interruption due to interference from other radio sources in the vicinity, including microwaves, bluetooth devices, WLAN devices (802.11b,g,n) and cordless phones. Depending on the strength and duration of the interference, the interruption may occur for an extended period. A loss of connection, due to moving out-of-range, interference, or for other reasons, is indicated with a No Host Monitoring INOP (here the host is the fetal monitor) on the NBP or SpO2 Pods, or a cl NBP Disconnect or cl SpO₂ Disconnect INOP at the fetal monitor. Correct channel configuration is important, see the Configuration Guide for details.1Docking slot for CL pods
3 Basic Operation49Rear and Bottom1Name plate1Manufacturer label2Cable reel
3 Basic Operation50Cableless TransducersThe cableless Avalon CL transducers have a built-in radio interface with an on-board, integrated antenna. The fetal monitor connected to the Avalon CL base station can control the transducer using radio communication. The transducer transmits measured values, alarms, and status information to the fetal monitor.The cableless transducers are assigned by simply docking them at the Avalon CL base station. If they are picked up from their docking slot at the base station, they are automatically activated.CAUTIONTo ensure the correct assignment of CL transducers to the fetal monitor in use, always dock them at the base station connected to that fetal monitor before use. This is particularly important when you add an additional CL transducer that was previously docked at another base station.1Transducer finder LED - lights up on the transducer providing the measurement source.2CL Toco+ MP transducers (additionally capable of providing the maternal pulse measurement)3Belt buttonCL Ultrasound transducer
3 Basic Operation51Radio Range of CL TransducersThe CL transducers have a operating range around the base station of at least 70 m in the line of sight. Obstructions as walls, metal doors, elevators and other environment structures can lead to signal loss. The Tele symbol indicator and the Tele Info window on the monitor's display (see “Screen Elements” on page 56 and “Tele Info Window” on page 92) provide information on the status of the signal strength. When a patient is approaching the end of range, the US sound is replaced by an artificial QRS sound (like DECG), and the DECG and MECG waves are no longer displayed on the monitor.Connector Cap for the CL Toco+ MP TransducerThe CL Toco+MP transducer is delivered with a connector cap covering the MECG/DECG/IUP connector. The connector cap is designed to cover the connector, not to protect it from water. (The connector itself is water-proof and may be immersed in water). You can reorder lost connector caps in a kit of 10 (989803184841).CL ECG/IUP transducer
3 Basic Operation52Cableless Transducer LED IndicationThe cableless transducers have a multi-color LED that indicates the status of the transducer with specific colors. This LED remains visible when the transducer is correctly attached to the transducer belt (Philips standard belt).1LEDLED Status MeaningWhite The LED lights up to identify the US transducer among other US transducers, and to easily verify the correct transducer assignment (transducer finder). The transducer finder LED is controlled by the fetal monitor. Click on the numerics to identify the corresponding US transducer. The LED also lights up when the mother is paged with the Call Patient SmartKey.White one short blink The LED shortly lights up to indicate that the transducer successfully opened a radio communication with the base station and that it is ready to use.Green The LED lights up green when the transducer is fully charged and docked at the base station.Yellow The LED lights up yellow when the transducer is charging and docked at the base station.Red The LED lights up red when the transducer is out of battery and has to be recharged.Cyan The LED lights up cyan to indicate a technical problem that needs your attention. Check your fetal monitor for a related INOP.
3 Basic Operation53CL Transducer BatteryBattery replacement is recommended after 500 charge/discharge cycles *2) or if the battery is older than 4 years whatever is reached first. If the battery of a cableless transducer has aged and an exchange of the battery is highly recommended, a prompt message is displayed at the fetal monitor for ca. 60 seconds. The prompt is repeated whenever the Tele Info window is opened until the battery is replaced.Depending on the transducer type the following messages are displayed:cl US battery has aged. Replacement strongly recommendedcl Toco battery has aged. Replacement strongly recommendedcl ECG/IUP batt has aged. Replacement strongly recommendedIf you are getting this message contact your service personnel so they can replace the CL transducer's battery. The date of manufacture and number of charge/discharge cycles can be inquired on the connected fetal monitor. For battery cycle and battery life specification of the CL pods (NBP and SpO2) please refer to the Service Guide of the Cableless Measurements.Charge CycleThe CL transducer batteries are designed for frequent recharging. A complete charging cycle is only reached and counted, when all recharging periods equal a 100% charge (900 mAh equal 8 hours continued operation). Audio Signal CL TransducersThe Avalon CL transducers have two audio signals:• If a tone sequence is played, the transducer was triggered by the fetal monitor to page the patient wearing it, or to locate a not docked transducer.• An INOP tone indicates that the transducer has detected a technical problem (INOP). Check your fetal monitor for a related INOP message.
3 Basic Operation54CL PodsThe two CL Pods provide measurement values for SpO2 and NBP on the built-in display, and communicate them to other system components using a wireless short range radio (SRR) interface. They are controlled with SRR from the Avalon CL base station and the connected fetal monitor.The maternal measurement pods are easily assigned by docking them at the Avalon CL base station.The SpO2 Pod and the NBP Pod have an LCD display and three keys for basic operation e.g. to assign the device to a patient:For further operational details read the IntelliVue Cableless Measurements Instruction for Use.CL NBP PodCL SpO2 Pod1Integrated LCD display2Hard keys3Measurement identifier
3 Basic Operation55Battery Status LED for CL PodsThe CL Pods do not have their own battery status LED. On the Avalon CL base station the battery status LED for the CL Pods is located directly under the docking slot.The battery status LED shows five different states:Audio SignalThe Avalon CL base station has audio signals to let you know when a transducer's battery has to be recharged, or if the base station cannot set up radio communication with a CL transducer or a CL Pod. Only active CL transducers and CL Pods emit an audio signal.• If the base station issues a descending tone sequence, the attempt to set up radio communication to a CL transducer or a CL Pod has failed.• If an interval tone is played, the battery of one or more the CL transducers or CL Pods need to be recharged.Operating and NavigatingYour monitor has a touchscreen. Everything you need to operate the monitor, except the on and off switch, is contained on its screen. Most screen elements are interactive. Screen elements include measurement numerics, screen keys, information fields, status indicators, alarms fields, and menus.OperatorPositionThe typical operator's position is in front of the monitor.1Battery status LED for CL PodsStatus MeaningGreen The docked CL Pod is fully charged.Yellow The docked CL Pod is charging.Yellow blinking The communication is established with the docked CL Pod.Cyan Indicates that the docked CL Pod or the charging slot has a technical problem that needs your attention. Check your fetal monitor for a related INOP message.Off The battery status LED is off, when no CL Pod is docked.
3 Basic Operation56FM40/50 If an optional external touch display is connected to the monitor, you can operate the monitor using the external touch display.Screen ElementsMonitor Information Line1Monitor Information line2Measurement area3Key area1LAN connection status indicator only. RS232 system connection is not indicated. The train icon indicates if the fetal monitor is connected to OB TraceVue/IntelliSpace Perinatal, via a LAN cable or not.2Patient identification3Date and time4Bed label (when connected to a Philips OB TraceVue/IntelliSpace Perinatal system)5Fetal heart sound volume adjust/indicator6Alarm volume adjust/indicator7INOP and alarm status area - shows active alarm messages
3 Basic Operation57Measurement Area1Antenna symbol (indicates a cableless measurement from a connected Avalon CL or Avalon CTS system).2Configurable alarm limits3NST test 4Audio source symbol5Measurement numeric6Alarms off symbol7Fetal trace recorder - status indicator8Avalon CL or Avalon CTS system - status indicator9Battery status indicator10 Status line - shows status and prompt messages11 Signal quality indicator: good, acceptable, poor12 Fetal heart rate measurement label13 Measurement unit (configurable)14 Cross-Channel Verification symbol (see “Cross-Channel Verification (CCV)” on page 149)15 NST timer, if configured (default is Off)
3 Basic Operation58Screen DetailsIcon DescriptionThe antenna symbol indicates a cableless measurement (Avalon CL or Avalon CTS).Indicates a short range radio measurement (IntelliVue CL Pods).Signal quality indicator:1Good2Acceptable3PoorFetal trace recorder - status indicatorFetal recorder is onFetal recorder is off (when Paper Save Mode is off)Fetal recorder is off (when Paper Save Mode is on)There is a user-solvable recorder error (paper out, paper jam, wrong paper scale set)Fetal recorder is defective: call serviceAvalon CL or Avalon CTS system - status indicator: An interface cable is connected to the monitor, a base station is connected, powered on, and at least one cableless transducer has been taken from the base station and is active. Any connected wired transducers are disabled.An interface cable is connected to the monitor, the base station is connected, powered on, and cableless transducers are ready to use, but no cableless transducers are currently active (all are still docked at the base station).An interface cable is connected to the monitor, but the base station is not connected to the interface cable, or it is disconnected from AC mains, or is in Standby mode.
3 Basic Operation59Key AreaKeysThe monitor has three different types of keys.Permanent KeysA permanent key is a graphical key that remains permanently on the screen, giving you fast access to functions.The CL transducer is moved away from the base station approaching the limit of the area of reach. The US sound is replaced by an artificial QRS sound (like DECG). The DECG and MECG waves are no longer displayed.1SmartKeys - these can vary according to your monitor's configuration2Main Screen - which closes all open menus and windows and returns to main screen3Scroll to display more SmartKeys4Silence - key which acknowledges all active alarms by switching off audible alarm indicatorsIcon DescriptionKey Name FunctionSilence Acknowledges all active alarms by switching off audible alarm indicators.Main Screen Closes all open menus and windows and returns to the main screen.
3 Basic Operation60SmartKeysSmartKeys are configurable graphical keys, located at the bottom of the main screen. They give you fast access to functions. The selection of SmartKeys available on your monitor depends on your monitor configuration, and on the options purchased.SmartKey Name FunctionMain Setup Enters main setup menuPause Alarms Pauses alarm indicators. Pause duration depends on monitor configuration. If the pause duration is infinite, this key is labeled Alarms OffSelect again to immediately re-enable alarm indicatorsStart Recordng Turns the trace recorder onRecord ECG Wave Starts printing the MECG, DECG or both waves, when both are availablePatient Demogr. Enters the patient identification menu to admit/dischargeQuickAdmit Quick admits the patient for monitoringToco Baseline Resets Toco baselineZero IUP Zeros IUP measurementStart/ Stop • Starts/stops manual noninvasive blood pressure measurement• Starts auto series• Stops current automatic measurement within seriesStart NBP • Starts manual noninvasive blood pressure measurement• Starts auto seriesRepeat Time Sets the time interval between two noninvasive blood pressure measurementsSound Vol. Up Increases the fetal heart rate volumeMonitor Standby Enters the Standby mode, suspends monitoring. All numerics and waves disappear from the display. All settings and patient data information are retained
3 Basic Operation61Recorder Start/ Stop Turns the trace recorder on or offPaper Advance Advances the paper automatically to the next foldStop Recordng Turns the trace recorder offStored Data Rec Prints trace data from the monitor's memoryEnter Notes Enters notesTimer Enters NST timer windowSet Marker Marks an eventStop All Stops all noninvasive blood pressure measurementsStop NBP Stops manual noninvasive blood pressure measurementStops current automatic measurement within seriesNBP Modes Access NBP mode selection and setup, with direct start/stop functionDefaults Loads User DefaultSound Vol. Down Decreases the Fetal Heart Rate volumeNST Report Initiates an NST trace interpretation and obtains a Non-stress test (NST) reportCall Patient Pages the patient. Only enabled if at least one CL transducer is currently activeTele Info Calls up the Tele Info windowEnter Temp Allows the manual input of the patient's temperatureSmartKey Name Function
3 Basic Operation62Pop-Up KeysPop-up keys are context-sensitive graphical keys that appear automatically on the monitor screen when required. E.g. the Confirm pop-up key appears when you need to confirm a change.Using the TouchscreenSelect screen elements by pressing them directly on the monitor's screen.Disabling Touchscreen Operation1To temporarily disable the touchscreen operation of the monitor, press and hold the Main Screen permanent key for about three seconds. A red padlock will blink on the Main Screen permanent key.2Press and hold the Main Screen permanent key again for about three seconds to re-enable the touchscreen operation.Operating ModesWhen you switch on the monitor, it starts up in Monitoring Mode. To change to a different mode:1Select the Main Setup menu.2Select Operating Modes and select a mode.Your monitor has four operating modes. Some are passcode protected.Mode Description Password ProtectedMonitoring Mode The Monitoring Mode is the normal operating mode to monitor patients. You can change elements such as alarm limits. When you discharge the patient, these elements return to their default values. You cannot select or change grayed out items. These items are for your information only. To change these items, switch to the Configuration Mode.noDemo Mode The Demo Mode is used for demonstration and training purposes. Do not change into Demo Mode during monitoring. When transducers are connected to the monitor and the recorder is on, a demo trace is recorded. But the demo trace is not transmitted to an information and surveillance system such as OB TraceVue/IntelliSpace Perinatal.yes
3 Basic Operation63A field displayed at the fetal monitor screen indicates if the monitor is in Demonstration Mode, Configuration Mode, or Service Mode. To change to a different mode, select this field.Automatic Screen LayoutsYour monitor's preconfigured screen layouts define how measurement information is arranged on the screen. The monitor automatically applies the correct screen layout for the measurements you are monitoring. No user action is required.Connecting or disconnecting transducers, or switching the noninvasive blood pressure measurement on or off, results in an automatic adjustment of the screen layout. When a measurement is off, its numerics are removed from the monitor's screen. The monitor stops acquiring data and generating alarms for this measurement. If you disconnect a transducer while it is performing a measurement, the monitor issues a disconnect INOP (and in the case of SpO2, replaces the measurement numeric with a question mark).SettingsThis section describes the various settings available on the monitor.Active SettingsWhat the monitor displays, and the way it operates, is controlled by its settings. They determine screen content, layout, high and low alarm limits and so forth.The "active settings" are the current settings the monitor uses, including any adjustments made by the last user. Active settings are not permanent, but are retained after a loss of mains power.There are also two preconfigured default settings:•User Default•Factory DefaultConfiguration Mode The Configuration Mode is for personnel trained in configuration tasks. You can change and store the default values and patient profiles permanently in the Configuration Mode. These tasks are described in the Configuration Guide. During installation, the fetal monitor is configured for use in your environment. This configuration defines the default settings you work with when you switch on the fetal monitor.yesService Mode The Service Mode is for trained and authorized service personnel only. yesMode Description Password Protected
3 Basic Operation64User DefaultThe User Default is a complete configuration stored in the monitor's long-term memory. You can store the active settings, modified to your preference, in the User Default (in Configuration Mode).In monitoring mode, you can load the User Default settings to return to your preferred settings:1Select the Defaults SmartKey 2Select Confirm in the dialog box to load the User Default.Factory DefaultThe Factory Default is a complete configuration pre-defined at the factory. You cannot modify it. In Configuration Mode, you can load the Factory Default as the active settings.CAUTIONThis resets all settings to factory defined values, but be aware that some values will differ from those with which the fetal monitor was originally shipped from the factory (recorder speed and paper scale type will need to be corrected, for instance). After loading the Factory Default, check the settings and, if necessary, change them to the settings you normally use.You can use the Factory Default as the basis for producing your User Default. See the Service Guide for details.Global SettingsGeneral monitor configuration settings are stored in the Global Settings. These include settings for line frequency, QRS type, and whether the monitor is automatically reset to the User Default after a power interruption of more than one minute. You can change the Global Settings in Configuration Mode.Changing Measurement SettingsEach measurement has a setup menu in which you can adjust all of its settings. You can enter a setup menu:1with the measurement numeric - select the measurement numeric on the screen to enter its setup menu. For example, to enter the Setup FHR1 menu, select the FHR1 (fetal heart rate 1) numeric.2with the Main Setup SmartKey - if you want to setup a measurement when the measurement is switched off, use the Main Setup SmartKey and select Measurements. Then select the measurement name from the pop-up list. With this SmartKey you can access any setup menu in the monitor.This guide always describes the entry method using the measurement's setup menu. You can use the method you prefer.
3 Basic Operation65Switching the Noninvasive Blood Pressure Measurement On and OffThe noninvasive blood pressure measurement is the only measurement that you can manually switch on and off. To do this:1Enter the noninvasive blood pressure measurement's setup menu.2Select NBP to toggle between on and off. The screen display indicates the active setting.Changing Monitor SettingsTo change monitor settings such as brightness, or touch tone volume:1Enter the Main Setup menu.2Select the setting you want to change, or select User Interface to enter a sub menu where you can change user interface settings.Adjusting the Screen Brightness1Enter the Main Setup menu.2Select User Interface.3Select Brightness.4Select the appropriate setting for the screen brightness. 10 is the brightest, 1 is the least bright. Optimum is suitable for most situations.Adjusting Touch Tone VolumeThe touch tone is the tone you hear when you select any field on the monitor screen. To adjust the touch tone volume:1Enter the Main Setup menu.2Select User Interface.3Select Touch ToneVolume, then select the appropriate setting for the touch tone volume: 10 is the loudest and 1 is the quietest. Selecting zero switches the touch tone volume off.Setting the Date and TimeThe current date and time is displayed in its own element in the information section of the monitor screen. 1Select the date and time screen element from the monitor's information line to enter the Date, Time menu.2Select, in turn, the Year, Month, Day, Hour (in 24 hour format) and Minute, as necessary.3Select Store Date, Time to change the date and time.
3 Basic Operation66WARNINGDo not change the date and time setting, if the fetal monitor is connected to a Philips OB TraceVue/IntelliSpace Perinatal system via a LAN -setup. The monitor uses the OB TraceVue/IntelliSpace Perinatal system date and time, including daylight saving time changes. As long as the fetal monitor is connected to the OB TraceVue/IntelliSpace Perinatal system via the LAN-setup (locomotive icon displayed on the monitor's screen), the option to change the date and time settings at the fetal monitor are disabled, this is not valid for RS232 connections, or the connection to other systems.When disconnected from AC power, the monitor retains the date and time setting for at least two months. If the monitor is off longer than two month, and the operating system detects that the date and time settings are invalid, the monitor initiates a "cold" start and sets the date to 1 Jan 1997 and the time to 00:00. Checking Your Monitor Revision1Select Main Setup, Revisions to open the Monitor Revision menu.2From the Monitor Revision menu, select the monitor component for which you need revision information.Preparing to MonitorConfirm fetal life before you begin fetal monitoring. Familiarize yourself with the basic operation principles before you start to monitor.CAUTIONCheck the fetal monitors housing for damage before you start to monitor as part of your safety precautions.After you switch on the monitor:1Check that you have the correct patient cables and transducers plugged in for the measurement you want to monitor.2If you use an Avalon CL or Avalon CTS system, check if the cableless transducers are ready and charged (apparent by either a lit up green or yellow LED indicator).3Admit your patient to the monitor (see “Admitting a Patient” on page 135).4Check that the alarm limits, alarm and fetal heart rate volumes, patient category, and so forth are appropriate for your patient. Change the settings if necessary.5Refer to the appropriate measurement section for details of how to perform the measurements you require.6Start recording.
3 Basic Operation67Switching On: FM20/FM30FM20/30 1Connect the monitor to AC mains and switch the monitor on.– The green power-on LED lights up.– The monitor performs a self-test as it starts up. Selftest: OK, the serial number, and revisions for the software and firmware are printed on the fetal trace paper (if recorder Auto Start is configured to On).– The monitor display comes on.– There is a start-up tone from the loudspeaker.FM20/30BatteryOption• If this option has been chosen, the green power-on LED on both the external power supply and the battery LED indicator will light up.Switching On: FM40/FM50FM40/50 1Connect the monitor to AC mains. – The green LED lights up.2Press the On/Standby switch.– The monitor performs a self-test as it starts up. Selftest: OK, the serial number, and revisions for the software and firmware are printed on the fetal trace paper (if recorder Auto Start is configured to On).– The monitor display comes on.– There is a start-up tone from the loudspeaker.Adjusting the Display Angle (FM20/FM30)FM20/30 You can tilt the display on the FM20 and FM30 to one of five different positions, or you can fold it completely down. The tilt/fold mechanism works on a one-way ratchet system. You hear a click as each of the five positions is reached. The screen can be folded back down only after tilting the display forwards as far as it will go.To tilt the display from the folded position:1Unlock the display by releasing the catch.
3 Basic Operation682Lift the display forward. You will hear a click as the first position engages. If you want to tilt the display further, lift the display further forward until you reach the desired angle.3To fold the display, pull the display forwards as far as it will go4Then push the display all the way back until it clicks shut.If your monitor is wall-mounted, the display should be folded flat.
3 Basic Operation69Fastening Belts and TransducersYou can use more than one belt if, for example, you are monitoring uterine activity and FHR simultaneously. There are two basic ways to fasten belts and transducers:• Belts with button fixings.• Velcro belts together with the butterfly belt clip.What You Need• Ultrasound transducer• Toco MP or CL Toco+MP transducer•Ultrasound gel• Transducer belt (and optional butterfly belt clip, if applicable)Using Belts with Button Fixings1Place the transducer belt across the bed, so that the fixing button will face away from the mother when it is fastened.2Lie the patient on the bed and arrange the belt around her until it is tight but still comfortable.3Fasten the belt by pushing the fixing button through the overlapping section of the belt. Ensure that the fixing button and the loose ends of the belt are at the patient's side.
3 Basic Operation704When you have positioned a transducer satisfactorily, you can attach it to the belt by pushing the belt button on the transducer through one of the holes in the belt.5Alternatively, attach the butterfly belt clip to the transducer belt button and use this to attach the transducer to the belt. The clip allows you to slide the transducer for easy repositioning.
3 Basic Operation71Using CL Transducers with a Belt ClipThe Avalon CL transducers have their own belt clip. They can be optional ordered in a kit of 10 (989803184851).Using Belt with Velcro FixingsInsert one end of the belt between the belt guides on one side of the butterfly belt clip, and secure with the velcro fixing. Insert the other end of the belt between the belt guides on the other side of the butterfly belt clip, adjust for the correct tension, then secure with the velcro fixing.WARNINGWhen connecting devices for acquiring measurements, always position cables and NBP tubing carefully to avoid entanglement or potential strangulation.1Avalon CL belt clip1Velcro fixing2Belt guides3Velcro fixing
3 Basic Operation72Repositioning TransducersA patient possibly wears transducers for long periods without interruption. In rare cases, skin irritations may occur if a transducer is attached to one location for a longer period. To ensure there are no adverse effects on the patient's skin, inspect the transducer application site at least every three hours. If the skin quality changes, move the transducer to another site.The ultrasound transducer is often repositioned to follow the fetal heart as part of the normal monitoring process, but this is not so for the Toco transducer. Therefore, remember to check its application site (between contractions) at least every three hours.To reduce the risk of skin irritations, do not allow a cleaning or disinfecting agent to remain on the transducer. Follow all instructions that accompany the specific cleaning and disinfecting agents you are using. Remove agent residues with a cloth dampened in water before applying a transducer to a patient.See “Care and Cleaning” on page 245 for further information, and a list of approved agents.Connecting a Transducer to the Monitor1SpO2 socket2Noninvasive blood pressure socket3Fetal sensor socketsYou can plug a fetal transducer, an ECG/IUP patient module, an Avalon CL or Avalon CTS Cableless Fetal Transducer System interface cable (red connector), or an external event marker into any of the four fetal sensor sockets marked by the fetal icon, or "Fetal Sensors" (depending on geography). For measuring maternal SpO2, connect the sensor to the socket marked with the SpO2 icon or "SpO2" (depending on geography).For maternal non-invasive blood pressure, connect the cuff to the socket marked with the NBP icon or "NBP" (depending on geography).
3 Basic Operation73For the FM20 and FM30, you can connect an Avalon CL Cableless Fetal Transducer system interface cable (red connector) to one of the fetal sensor sockets at the left side of the monitor.For the FM40 and FM50, you can connect an Avalon CL or Avalon CTS Cableless Fetal Transducer System interface cable (black connector) to one of the two dedicated black sockets marked "Tele" at the rear of the monitor, as an alternative to using one of the fetal sensor sockets (red connector) at the front.What You See on the MonitorWhen you connect a transducer or sensor, the measurement numeric appears on the screen. Fetal heart rate measurements are labeled in the order in which you plug in the transducers for those measurements. It does not matter which fetal sensor socket you use, as the monitor allocates a channel automatically. For instance, when monitoring triplets, the first transducer you connect is automatically allocated a channel, and the measurement is labeled FHR1, the second FHR2, and the third FHR3. See also chapters “Monitoring Twin FHRs” on page 171 and “Monitoring Triple FHRs” on page 179.When you touch a measurement numeric on the screen, the setup menu for that measurement opens. The fetal sensor socket to which the transducer for this measurement is connected is identified by the transducer position indicator in the blue setup menu header.1Interface cable to Avalon CL and Avalon CTS Cableless Fetal Transducer System.2Connect the black connector to one of the two black sockets (marked "Tele") on the rear of the monitor.for FM20/FM30 for FM40/FM50
3 Basic Operation74The blue finder LED on a wired fetal transducer lights up when you touch the measurement on the screen, allowing you to identify the corresponding transducer.The white finder LED on a cableless fetal transducer lights up when you touch the measurement on the screen, allowing you to identify the corresponding transducer.The recorder prints an annotation showing the date, time, paper speed, and monitoring mode. It repeats this every 10 minutes.Start RecordingChecking/Setting Paper ScaleYou can check the paper Scale Type (US for USA, or Internat'l for other geographies) in the Fetal Recorder menu. In Monitoring Mode, you can see these settings (grayed out), but you cannot change them. They can be changed in Configuration Mode, see the Configuration Guide.1Finder LED1Finder LED cableless transducer
3 Basic Operation75Paper Guide FM40/FM50FM40/50 The recorder in the FM40 and FM50 features a transparent paper guide which:• facilitates correct alignment of the paper, both during loading and while the recorder is running. See “Loading Paper FM40/FM50” on page 84.• incorporates a tear-off edge, which not only allows you to tear off the trace paper where you like (not necessarily at a fold), but also helps to avoid paper misalignment while doing so (see “Tearing Off the Paper” on page 80).• is removable (see “Removing the Paper Guide: FM40/FM50” on page 250).Switching the Recorder On and OffIn addition to the normal recording of real-time traces, you will sometimes see a trace recovery printout from the monitor's internal backup memory at high speed when the recorder is started. For details, see “Recovering Traces on Paper” on page 241.For an explanation of the various symbols that can appear on the trace recording, see “Recorder Specifications” on page 284.To switch the recorder on, select in Main Setup the menu item Fetal Recorder, or press one of the SmartKeys: Start/ Stop or Start Recordng.The "recorder on" status indicator is displayed in the bottom right-hand corner of the screen when you switch on the recorder.The paper advances quickly for 2 cm and then returns to the set speed. Whenever the recorder is switched on, a trace header is printed vertically on the trace paper, containing the following:•Selftest: OK: confirmation that the monitor's self-test completed successfully, and that it is ready to use.• the software revision and firmware revision•the serial number•the time•the date• patient name and medical record number (if entered)
3 Basic Operation76•the Recorder SpeedThe current monitoring modes (if any transducers are connected to the monitor) are printed. Whenever a transducer's mode is changed, the following are printed:•the time•the date• trace identification symbols•the Recorder SpeedThe monitor prints the time, date, Recorder Speed, and monitoring modes in the trace header when first switched on, in a periodic time stamp every ten minutes after, and if the monitoring modes change. The time stamp begins with the symbol shown below. The data is reprinted in the header if the 1Fetal heart rate label2Uterine activity label
3 Basic Operation77time and date are locally adjusted, or if an OB system is connected that readjusts the time and date automatically.The trace records maternal parameters also. When measuring noninvasive blood pressure, the annotation is made at the end of the measurement. If the noninvasive blood pressure measurement repetition time is short, the noninvasive blood pressure numeric may not always be printed.The recording of notes (see “Entering Notes” on page 88) or time/date information may be interrupted by connecting, or unplugging a transducer, or by a change in measurement-related setting (for example, artifact suppression, Toco sensitivity, or alarm settings).A new patient admission or a change to the paper scale setting stops all annotations, and prompts a new vertical trace header to be printed.To switch off the recorder:1Either select Start/Stop from the Fetal Recorder menu.2Or press one of the SmartKeys (depending on configuration): fetal recorder Start/ Stop or Stop Recordng.If your recorder is configured with Confirmed Stop on (a Configuration Mode setting), you will need to confirm that you want to stop the recorder, before it will stop.When the recorder is off, the "recorder off" status indicator is displayed in the bottom right-hand corner of the screen: When the Paper Save Mode is set to Off the paper icon shows an x mark, and when Paper Save Mode is On the icon shows a paper trace icon.1Time stamp printed every ten minutes
3 Basic Operation78Recording ElementsThe trace paper of the recorder has much information printed on it. Here is an exemplary trace with the most common print outs and their meaning. Each trace header contains the last name and first name, the patient ID, patient date of birth, the current date and time, patient's bed label, and the gestational age of the pregnancy.1Name, patient ID, date of birth, current date and time 2Recorder Speed3Gestational age and patient bed label4FMP - Fetal Movement Profile5Other measurement for the patient such as temperature, arterial oxygen saturation, and pulse.6Entered notes such as patient repositioned, or MD notified, or others7Time stamp8Trace separation9Recorder Speed10 Maternal ECG11 Direct ECG12 Coincidence of heart rate detected13 HR with Cross Bell14 Alarm Limits15 DFHR2 (second fetal heart rate from DECG)16 FHR1 (first fetal heart rate)
3 Basic Operation79Choosing Paper SpeedYou can choose a Recorder Speed of 1, 2, or 3 centimeters per minute (cm/min). The default setting is 3 cm/min.The ACOG technical bulletin on FHR monitoring states that "accurate pattern recognition is difficult if not impossible at 1 cm/min and that 1 cm/min is only recommended for more economic screening. When FHR abnormalities arise, the faster paper speeds will enhance FHR pattern recognition".Additionally, because a change in Recorder Speed results in a change in the appearance of an FHR trace, you are advised to ensure ALL monitors in your institution are set to the same speed.To set the Recorder Speed (in Configuration Mode) see the Configuration Guide.Advancing the PaperYou can advance the paper automatically to the next fold by pressing the Paper Advance SmartKey at any time except during a stored data recording. This is also possible using the Fetal Recorder menu.Marking an EventYou can record significant events on the trace paper (for example, when pain medication is administered or when the mother changes position). The mother can use the remote event marker to mark events herself. You connect the remote event marker to any free fetal sensor socket.To mark an event on the trace paper you can:1Either select the Set Marker SmartKey.2Or press the button on the remote event marker. The remote event marker is connected to the monitor via any fetal transducer socket.A small arrow is printed on the heart rate scale on the trace paper.
3 Basic Operation80This reflects exactly when the marker button was first pressed; keeping the button pressed has no influence on the annotation.Tearing Off the PaperCAUTIONNever pull on the paper to advance it, as this can cause misalignment of the paper. Always tear off the paper along the perforation.FM40/FM50 The recorder's paper guide incorporates a tear-off edge, allowing you to tear off the trace paper cleanly where you like (not necessarily at a fold). When not using the paper guide, always tear off the paper along the perforation.To tear off the trace paper after monitoring using the paper guide:1If the recorder is running (the "recorder on" status indicator is displayed), turn off the recorder by selecting the fetal recorder Start/ Stop SmartKey or the Stop Recordng SmartKey.
3 Basic Operation812Tear off the paper as shown in the picture. To ensure a clean tear, always tear in an upwards motion, as indicated by the arrows. You can start tearing from the left or right (right-handed user shown). You may want to use both hands to guarantee that the paper is not misaligned during the tear off.3If you wish to tear off the paper at a fold, select the Paper Advance SmartKey, wait for the paper to stop, then tear it off.FM20/FM30 The FM20/FM30 does not have a paper guide. The procedure is the same as described for the FM40/FM50 with the exception that you should advance the paper to a perforation. If you wish to tear off the paper at a perforation, select the Paper Advance SmartKey, wait for the paper to stop, then tear it off.Paper-Out IndicationEach pack of paper has 150 pages. The monitor issues a paper-out warning in the status line at the bottom of the screen, when there are five pages to go. If you switch on the recorder or press the paper advance key when there are fewer than five pages remaining, it may take two pages before the alarm is activated. Load a new pack in time.If the recorder runs out of paper, an audible paper-out alarm is sounded, if so configured. See “Loading Paper FM40/FM50” on page 84and “Loading Paper FM20/FM30” on page 82 to learn how to reload paper. Fetal traces continue to be recorded into the monitor's backup memory, and can be retrieved and printed completely if new paper is loaded within one hour, when the Bridge Paperout setting is enabled in Configuration Mode. See “Recovering Traces on Paper” on page 241 for further information.
3 Basic Operation82Loading Paper FM20/FM30CAUTIONUsing recorder paper that is not approved by Philips can result in accelerated paper fading and can damage the thermal line printhead. This type of damage is not covered by warranty.FM20/FM30 To load a pack of paper:1If the recorder is on, press the recorder Start/ Stop SmartKey or the Stop Recordng SmartKey to turn it off before loading a new pack of paper.1Press the paper table release to unlock the paper drawer and then pull the table forward to open it fully.2Lift out any remaining paper from the tray.3Prepare to place the new pack of paper in the tray with the bottom side down. The bottom side is indicated by the word STOP printed on the final page of the new pack.
3 Basic Operation834Unfold the top page of the pack and position the uterine activity scale on the right.5Slide the pack into the tray.
3 Basic Operation846Push the paper drawer back until it "clicks" closed.7Press the recorder Start/ Stop SmartKey or the Start Recordng SmartKey to switch on the recorder.Annotations of trace information are printed on the trace paper (see “Switching the Recorder On and Off ” on page 75 for details).Loading Paper FM40/FM50CAUTIONUsing recorder paper that is not approved by Philips can result in accelerated paper fading and can damage the thermal line printhead. This type of damage is not covered by warranty.FM40/FM50 To load a pack of paper:1If the recorder is on, press the Start/ Stop Rec SmartKey or the Stop Recordng SmartKey to turn it off before loading a new pack of paper.
3 Basic Operation852Press the paper eject button to open the paper drawer.3Lift out any remaining paper from the tray. 4Press and hold the paper eject button to partially eject the paper, thus making it easier to remove.5Hinge the transparent paper guide forward. It is held in the closed position by a small protrusion on each side of the holder.
3 Basic Operation866A - Protrusion holds paper guide in closed position.7Prepare to place the new pack of paper in the tray with the bottom side down. The bottom side is indicated by the word STOP printed on the final page of the new pack.8Unfold the top page of the pack and position the uterine activity scale on the right.9Slide the pack into the tray.
3 Basic Operation8710 Feed the paper evenly through the paper guide. Do not close the paper guide yet.11 Close the paper drawer.12 Now close the paper guide.
3 Basic Operation8813 Press the recorder Start/ Stop SmartKey or the Start Recordng SmartKey to switch on the recorder.Annotations of trace information are printed on the trace paper (see “Switching the Recorder On and Off ” on page 75 for details).Entering NotesYour monitor has a set of 15 factory pre-configured notes (see below). The maximum length of one single note is 30 characters. It is possible to edit the notes in Configuration mode (see the Configuration Guide).To enter a note:1Press the Enter Notes SmartKey to open the Enter Note menu.2Scroll if necessary, then select the note you wish to enter. A confirmation dialog box opens:3Select Confirm to enter the note. The note is then shown in the status line of the display, and is annotated on the fetal trace if the fetal recorder is on.
3 Basic Operation894By default, notes are printed lengthwise in the direction of the trace, in the space between the FHR grid and the uterine activity grid. If you prefer, you can configure the recorder to print across the trace.5You can change this in Configuration Mode by changing the Notes Recording setting in the Fetal Recorder menu from Along (default) to Across (notes print width wise across the trace).The following are the pre-configured notes from which to choose:1Patient Repositioned2Vaginal Examination3MD Notified4Sitting5On Back6Left Lateral7Ambulating8Tocolytic Given9Membranes Ruptured10 Amniotomy11 Amniotic Fluid Clear12 Amniotic Fluid Not Clear13 Oxytocin14 Urinary Catheter15 Micro Blood AnalysisUp to two notes can be printed directly, and the monitor can temporarily store up to a further two notes, and these are printed after the first two have been recorded. Any further notes are discarded. For example, if you enter six notes in quick succession, the first two notes you entered are recorded right away, the next two are stored in memory and then printed when the first two have been recorded, and the last two are discarded.If the printing of two notes happens to coincide with the regular recording of the time stamp that takes place once every ten minutes, the time stamp is delayed until the notes have finished printing.Signal QualityDuring monitoring, if the fetal heart rate signal quality fluctuates, and becomes poor, it does not necessarily mean that the transducer needs repositioning. The fluctuation may be caused by fetal movement. Allow time for the signal to stabilize before deciding whether to reposition the transducer (ultrasound), or apply a new electrode (ECG). For the best trace quality, the signal quality indicator should be full, indicating good signal quality, even though it may be possible to make traces at a lower signal quality level.
3 Basic Operation90Cableless MonitoringBasics of Cableless SystemsThe fetal monitors FM20/FM30 and FM40/FM50 are compatible with the Avalon CL and Avalon CTS Cableless Fetal Transducer system. Regard the following points for cableless monitoring:• You can connect one Avalon CL with a red connector to a FM20/FM30 or a FM40/FM50 (fetal socket).• You can connect up to two Avalon CLs with a black connector to a FM40/FM50 (Tele socket).• You can connect one Avalon CTS system to a FM20/FM30 or FM40/FM50 at a time (either fetal or Tele socket).•You cannot connect Avalon CTS and an Avalon CL at the same time to the same fetal monitor. • Monitoring multiple pregnancy using cableless transducers is supported by the Avalon CL system only.• Using a mixture of wired and cableless fetal transducers is not supported. You can use either wired or cableless fetal transducers. • If you cannot get sufficient signal quality using Avalon CTS transducers, switch to wired transducers.Assigning Cableless TransducersThe cableless transducers of the Avalon CL are assigned by simply docking them at the base station connected to the patient’s fetal monitor. See the Avalon CTS Instruction for Use for the assignment of the cableless transducers of this system.Avalon CL Transducer System Avalon CTS Transducer System
3 Basic Operation91Activating Cableless TransducersThe CL transducers of the Avalon CL are activated by picking them up from the base station. If the CL transducer is activated, an antenna symbol is displayed on the fetal monitor screen next to the numeric of the measurement. See the Avalon CTS Instruction for Use for the activation of the cableless transducers of this system.Unassigning Cableless TransducersThe CL transducers of the Avalon CL are unassigned by manually removing them in the corresponding setup menu from the group of assigned cableless devices, or by unassigning them directly in the Tele Info window. See the Avalon CTS Instruction for Use for the unassignment of the cableless transducers of this system.Deactivating Cableless TransducersThe CL transducers of the Avalon CL are deactivated by redocking them at a base station. To deactivate all cableless transducers at once press the Standby button of the Avalon CL base station. See the Avalon CTS Instruction for Use for the deactivation of the cableless transducers of this system. Configuration of Cableless SystemsFor the Avalon CL and Avalon CTS Cableless Fetal Transducer system and the corresponding channels have to be configured for the radio communication to work and not to interfere with any other telemetry devices. The configuration of a connected Avalon CL system is done in Configuration Mode or Service Mode of the fetal monitor. Service Mode functions can be used to identify channel assignment conflicts in the hospital environment. The configuration should be carried out by authorized and qualified service personnel, either by the hospital's biomedical department, or by Philips Support.For a detailed description of the configuration see the Avalon CL Service Guide and the Fetal Monitor Configuration Guide. For details regarding the configuration of a connected Avalon CTS system see the Avalon CTS Service Guide.Setup OBRRevisions A.00.00Frequency BandChannelWMTS4Scan DurationStart ScanStop Scan15 minStart RSSI TraceStop RSSI Trace
3 Basic Operation92Tele Info WindowThe Tele Info window of the fetal monitors allows you to manage the Avalon CL system. Below is an exemplary view of the Tele Info window. Your window may differ depending on the status of the connected system.To open the Tele Info window you can:1Configure a Tele Info SmartKey to open the window,2click on the TELE icon on the main screen, or3select the Main Setup and then Tele Info.1Transducer icon assigned with the parameter label2Cableless module icon and equipment ID3Base station icon with docking indication (the white slot indicates a charging transducer)4Key Remove5Key Find6Key Battery Report7Tele icon8Remaining battery time9Out of battery icon10 Indication of signal quality
3 Basic Operation93TelemetryWhen the monitor recognizes a connected Avalon CL or Avalon CTS interface cable (red or black connector), it confirms the recognition with the following status indicators displayed in the lower right-hand corner of the screen:NOTEA cableless transducer is considered still active, even if it has an INOP condition (e.g. cl US Disconnect), until it is either deactivated by docking it at the base station, or until it is manually removed from the Tele Info window.CL transducers have priority over wired transducers. If an Avalon CL or Avalon CTS base station is connected to the fetal monitor, and both wired and cableless transducers are connected to the monitor, the wired transducers are disabled whenever one cableless transducer is active. If an CL Pod is activated it does not automatically deactivate all wired transducers, just the one with the corresponding measurement.To switch back to using wired transducers, redock the cableless transducers at the base station, or switch the base station to Standby mode, and continue monitoring with the wired transducers. If you cannot get sufficient ultrasound signal quality using the Avalon CTS base station, try repositioning the transducers, or switch to wired transducers. Using a Avalon CL base station you should get a better signal by reducing the distance between CL transducer and base station.• When using an Avalon CL or Avalon CTS you should be aware that FMP is not recommended when the mother is likely to move, and you should disable Fetal Movement Profile (FMP) on the fetal monitor (Fetal Movement Off) if the mother is walking. Maternal movements are likely to create artifact in the FMP output. See also “Switching FMP On and Off ” on page 161, the sections “Cableless Monitoring - Important Considerations” on page 156 and “Fetal Movement Profile” on page 160.Indicator Avalon CTS Avalon CLAvalon CTS interface cable is connected to the monitor, but the Avalon CTS base station is not connected to the interface cable, or it is disconnected from AC mains, or is in Standby mode.A base station is connected to the monitor, but the base station is in Standby mode.Avalon CTS interface cable is connected to the monitor, Avalon CTS base station is connected, powered on, and cableless transducers are ready to use, but no cableless transducers are currently active (all are still docked at the base station).A base station is connected to the monitor but no cableless transducers and no cableless Pods are currently active. All are still docked at the base station, or the base station holds no transducers.Avalon CTS interface cable is connected to the monitor, Avalon CTS base station is connected, powered on, and at least one cableless transducer is active and assigned.A base station is connected to the monitor, it is on, and minimum one cableless transducer or cableless Pod is active and assigned.Not applicable for Avalon CTS. The CL transducer is moved away from the base station approaching the end of range (at least 70 m). The US sound is replaced by an artificial QRS sound (like DECG). The DECG and MECG waves are no longer displayed.
3 Basic Operation94• With the Avalon CL Transducer system you can now monitor twins and triplets with CL transducers. The Avalon CTS System does not have this option.About RF Signal QualitySignal transmission can be disturbed if:• the patient is out of range of the receiving area.• there is interference from another, possibly stronger, RF signal (a broadcasting station, for instance).• the patient is near material that absorbs electromagnetic waves (for example, metal-reinforced concrete, elevator doors) or the base station antenna is in an enclosed metal rack.Pop-up KeysPromptsThe fetal monitor issues prompt messages to certain user interactions. For example if the CL SpO2 Pod is picked up from the base station to activate it, the monitor displays the prompt message cl SpO₂ Added and the equipment lable of the Pod.CL Transducer AssignmentThe cableless transducers of the Avalon CL are assigned by simply docking them at the base station connected to the patient’s fetal monitor. Since twins and triplets can be monitored with the Avalon CL base station, it can be delivered with up to seven CL transducers: one CL Toco+MP, three CL US, and three CL ECG/IUP transducers. Only up to four CL transducer can be assigned at one time to the Avalon CL base station. Four assigned CL transducers enable monitoring combinations such as 1 CL Toco+MP transducer + 3 CL US transducers for monitoring triplets externally, or 1 CL Toco+MP transducer + 2 CL US transducer + 1 CL ECG/IUP transducer for monitoring twins.Pop-Up Key FunctionRemove Selecting the Remove key deactivates and unassigns the selected active transducer or cableless Pod and removes it from the list. This key is disabled if no active device is selected.Find Selecting the Find key pages the selected active CL transducer or CL Pod. This key is disabled if no active device is selected.Battery Report Selecting the Battery Report key prints a combined battery report on the built in recorder. The report contains at least the following information for each CL transducer or CL Pod currently in the list:• Cableless device identification (like in the Tele Info window list)• Battery identification (e.g. part no.)• Battery serial number• Battery manufacturing date• Battery capacity: remaining/when fully charged/battery temperature• Number of cyclesThis key is only available and enabled in Service mode.
3 Basic Operation95Three CL transducers can be docked and charged at the Avalon CL base station at the time. If a fourth transducer should be assigned to the Avalon CL base station:1Remove first the three already docked CL transducers from the base station and place them on the patient. 2Then dock the remaining fourth transducer at the base station and wait until the LED of the fourth transducer signals that it has communication with the base station.3Place the fourth CL transducer on the patient and check on the fetal monitor in the Tele Info window if the base station and the monitor have communication with all four transducers, and if their numerics are displayed on the screen of the fetal monitor.CL Transducer UnassignmentThe cableless transducer are not unassigned by simply removing them from the base station. To unassign a cableless transducer, there are two methods:1Open the setup menu of the measurement e.g. FHR1 by pressing the numeric on the screen. 2Select Remove from the open setup menu.3A confirmation window opens with the prompt Please Confirm and Device will be removed.4Press the pop-up key Confirm. A prompt states then clDev has been removed.or1Open the Tele Info window.2Select the symbol of the cableless transducer you want to unassign, and select Remove from the pop-up menu. 3A confirmation window opens with the prompt Please Confirm and Device will be removed.4Press the pop-up key Confirm. A prompt states then clDev has been removed.NOTEWhen a cableless transducer is unassigned, all the measurements from this transducer are no longer monitored; e.g. if you unassign a CL Toco+MP, the Toco measurement, SpO2, and MECG are possibly no longer monitored. CL Pods AssignmentThe cableless Pods of the Avalon CL are assigned by simply docking them at the base station connected to the patient’s fetal monitor. CL Pods UnassignmentTo unassign a cableless Pods, there are four methods:1Open the setup menu of the measurement e.g. SpO₂ by pressing the numeric on the screen. 2Select Remove from the open setup menu.3A confirmation window opens with the prompt Please Confirm and Device will be removed.4Press the pop-up key Confirm. A prompt states then clDev has been removed.or1Open the Tele Info window.2Select the symbol of the cableless Pod you want to unassign, and select Remove from the pop-up menu.
3 Basic Operation963A confirmation window opens with the prompt Please Confirm and Device will be removed.4Press the pop-up key Confirm. A prompt states then clDev has been removed.orUnassign the cableless Pods via it's user interface. See the Cableless Measurement Instruction for Use.or Dock the cableless Pod at another base station or charger and therefore assigning it to the new device.Paging PatientsTo page a patient currently not near the fetal monitor and base station select the SmartKey Call Patient at the fetal monitor. The base station will then select the cableless transducer with the best signal quality to emit the tone sequence to notify the patient.Underwater MonitoringOnly the cableless transducers of the Avalon CL and Avalon CTS systems can be used to monitor under water. You can use them to monitor patients in a bathtub or shower. This does not apply to the maternal cableless SpO2 and NBP Pods, do not immerse the CL Pods into water. Cableless transmission distances are shorter when monitoring under water. A metal bathtub is likely to further reduce the operating range.WARNINGNever immerse the base station in liquid. You must protect it against water sprays or splashes. Place the base station where there is no chance of contact with, or falling into water or other liquids. CAUTIONAvoid the use of pulsating water jets in the bath or shower while monitoring, as these can be misinterpreted as an incorrect (or totally artificial) heart rate.Toco Baseline drift: The accuracy specified for baseline drift cannot be guaranteed for underwater usage. When using transducers under warm water the temperature increase causes a significant baseline change due to internal pressure increase. The depth under water at which the Toco transducer is used also has an effect on the Toco baseline, as the water pressure increases with depth. After immersion, allow one to two minutes for the pressure to stabilize, then adjust the Toco baseline (between contractions), and check it frequently.When using the transducers underwater, the radio transmission range is reduced, and signal loss may occur.Water-proof belts like M1562B are recommended for the cableless transducers when monitoring in water.
397Switching the Monitor to StandbyTo switch the monitor to Standby:Either 1Select the Monitor Standby SmartKey.Or1Enter the Main Setup menu using the SmartKey.2Select Monitor Standby.3Pressing any key or selecting any field on the screen will resume monitoring.NoteIf a Avalon CL base station is connected to your FM 20/30 monitor, do not turn off the monitor if you need to recharge the batteries of the CL transducers. They can only be recharged if the FM20/30 monitor is on. If an Avalon CL base station is connected to an FM40/50, the batteries of the CL transducers can be recharged while the monitor is in Standby mode.After Monitoring1Discharge the patient.2Remove the transducer from the patient and, using a soft tissue, remove any gel from it. Then clean the transducer.3Dock CL transducers to their base station so they can recharge.4Tear off the paper at the fold. To avoid misalignment of the recorder mechanism, NEVER pull on the paper to advance it, or try to tear it other than at a fold (unless using the paper guide with the FM40/FM50).5Switch off the monitor.
3 Basic Operation98Disconnecting from PowerFM20/30 To disconnect the monitor from AC power, switch the monitor off using the On/Off switch located on the right side of the device, or unplug the power cord from the AC mains socket.FM40/FM50and FM20/FM30 withBatteryOptionThe On/Standby button does not disconnect the monitor from the AC power source. To disconnect, unplug the power cord from the AC mains socket. Note that if the power cord is unplugged from the AC mains socket before the monitor is put into Standby, a beeper is activated. The beeper warns you if the monitor is accidentally disconnected from AC mains.Power On/Power Off BehaviorThe general rules determining the behavior of the fetal monitors when connected to, or disconnected from power are as follows:• A fetal monitor that was switched on prior to a temporary power loss, switches on again when power is restored.• A fetal monitor that was switched off prior to a temporary power loss, remains off when power is restored.• When AC mains power is lost, a battery powered monitor (FM20/30) continues to run without interruption on battery power.Monitoring After a Power Failure• A fetal monitor that was switched on prior to a temporary power loss switches on again when power is restored.• A fetal monitor that was switched off prior to a temporary power loss remains off when power is restored.• If the fetal monitor is without power for less than one minute, monitoring will resume with all active settings unchanged.• If the fetal monitor is without power for more than one minute, the behavior depends on your configuration. –If Automat. Default is set to Yes, the default profile will be loaded when power is restored. –If Automat. Default is set to No, all active settings are retained, if power is restored within 48 hours. The Automat. Default setting is made in Configuration Mode.
3 Basic Operation99TroubleshootingProblem Possible Causes SolutionsLight or no trace. Wrong paper. Use recommended paper.Dirty printhead. Clean printhead. See “Cleaning the Print Head” on page 255.FM20/30 only: Paper misaligned due to drawer not being correctly shut.Shut the drawer fully, pushing evenly with both hands.End of paper noted when pack not finished.Bad paper feed or wrong paper. Check paper feed and use recommended paper.Check Paper INOP is displayed. INOP messages always indicate equipment problems.See “Patient Alarms and INOPs” on page 121.FetRec Equip Malf INOP is displayed.Paper End INOP is displayed.Wrong Paper Scale INOP is displayed.
3 Basic Operation100
4 FM20/30 Battery Option1014FM20/30 Battery OptionYou can switch between battery-powered and mains-powered (AC) operation without interrupting monitoring.The monitor is connected to the AC mains power via the external power supply.NOTEThe battery option is not available for the FM40/FM50.External Power Supply M8023AThe external power supply M8023A (option #E25) allows you to operate the fetal monitor from an AC (alternating current) power source of 100 V to 240 V (± 10%) and 50/60 Hz (± 5%). If this option is used, then the M8023A (option #E25) power supply is included for FM20/30.1AC power cord. Connect to AC mains socket.2Measurement Link (MSL) cable. Supplies power to the monitor for operation and for battery charging.3Power-on LED. The green light is on when the external power supply is connected to AC mains.
4 FM20/30 Battery Option102WARNING• Always use the supplied power cord with the earthed mains plug to connect the external power supply M8023A (option #E25) to an earthed AC mains socket. Never adapt the mains plug from the power supply to fit an unearthed AC mains socket.• Do not use AC mains extension cords or multiple portable socket-outlets. If a multiple portable socket-outlet without an approved isolation transformer is used, the interruption of its protective earthing may result in enclosure leakage currents equal to the sum of the individual earth leakage currents, so exceeding allowable limits.• Do not connect any devices that are not supported as part of a system.• Any non-medical device placed and operated in the patient’s vicinity must be powered via an approved isolation transformer that ensures mechanical fixing of the power cords and covering of any unused power outlets.Using BatteriesThe Lithium Ion batteries used in your monitor store a large amount of energy in a small package. This allows reliable battery-operated monitoring but also requires care in use and handling of the batteries. Follow the instructions in this chapter and see the Service Guide for further details.Battery Power IndicatorsThe battery LED and battery status information on the Main Screen, in combination with INOP messages and prompts, help you keep track of the battery power status. The indicators always show the remaining capacity in relation to the battery's actual maximum capacity, which may lessen as the battery ages. You can see the actual capacity in the Battery Status window.Battery LEDThe possible battery LED status on the right side of the monitor is described in the table below.
4 FM20/30 Battery Option103Battery Status on the Main ScreenBattery status information is permanently displayed on all screens. It shows the status of the battery, with the battery power remaining, with an estimate of the monitoring time this represents. Battery power gauge: This shows the remaining battery power. It is divided into sections, each representing 20% of the total power. If three sections are filled, as in this example, this indicates that 60% battery power remains. If no data is available from the battery, a question mark is shown in the gauge.Monitoring Time Available: Below the battery power gauge a time is displayed. This is the estimated monitoring time available with the current battery power. Note that this time fluctuates depending on the system load (the display brightness, the recorder configuration, and how many measurements you carry out).Battery malfunction symbols: Normal battery function is indicated by the battery power gauge, together with the remaining operating time, on the main screen. You are informed of problems or changes in the status of the battery by the battery status/malfunction indicator. This consists of a blank battery gauge containing a "!" symbol. If the symbol is red, this indicates a critical situation. You can check the specific cause of the problem by looking at the symbol(s) displayed in the Battery Status window.Battery LED Colors If the monitor is connected to mains power, this meansIf the monitor is running on battery power, this meansGreen Battery power is > 90%Yellow Battery charging (battery power < 90%)Red, flashing Less than 10 minutes power remainingRed, flashes intermittently Battery or charger malfunction Battery malfunctionBattery Status Indicator Battery Malfunction IndicatorAlternates with the battery gauge on the main screen.Check in the Battery Status window to see which status symbol is displayed to identify the cause.The red exclamation mark flashes. Critical battery situation or malfunction. Check in the Battery Status window to see which malfunction indicator is displayed, or refer to the INOP, to identify the cause.
4 FM20/30 Battery Option104Battery Status Window1To access the Battery Status window and its associated pop-up keys, select the battery status information on the screen, or select Main Setup, Battery.–Capacity, remaining tells you how much power is left in the battery.–Capacity, fullCharge tells you how much power the battery can hold when fully charged.–TimeToEmpty tells you approximately how long you can continue to use the monitor without an AC connection. The time span fluctuates depending on the system load (the display brightness and how many measurements you carry out), and the remaining capacity of the battery.–TimeToFull is shown in place of TimeToEmpty if the monitor is connected to a power supply, and tells you how much time is left until the battery is charged to 90%. If >10 hrs is shown here, the battery may not charge completely when the monitor is in use.Battery status/malfunction symbols: If a problem is detected with the battery, an INOP may be issued, and the following symbols are displayed in the Battery Status window, where they may be accompanied by a status message providing more details.Symbols indicating critical situations are colored red.Battery Status Symbols Battery Malfunction SymbolsBattery is empty (Red) incompatible batteryBattery not charging as the temperature is above or below the specified range(Red) battery malfunctionBattery requires maintenance (Red) battery has no power leftCharging stopped to protect the battery(Red) battery temperature too high(Red) battery is missing, insert battery
4105Checking Battery ChargeTo check the charge status of a battery, refer to the battery power gauge on the screen, or open the Battery Status window.When Battery Lifetime is ExpiredWhen the battery is aged, either after 3 years from manufacturing date or after 500 charge/discharge cycles, it is recommended to replace the battery. To remind you of this, a message will appear in the Battery Status window. This message will only be displayed at the appropriate time when the date and time on the monitor is correct.Optimizing Battery PerformanceThe performance of rechargeable batteries may deteriorate over time. Battery maintenance as recommended here can help to slow down this process.Display Brightness Setting1In the Main Setup menu, select User Interface, Brightness, then Optimum. This selects a level of brightness suitable for most monitoring locations that uses less battery power than brighter settings.2Ensure that the current level of brightness is suitable for your monitoring location.Charging the BatteryTo charge the battery,1Connect the monitor to the external power supply (M8023A).2Charge the battery until it is full, the battery LED is green, and the battery power gauge is filled.During high load of the monitor (usage of multiple measurements) the battery may not charge. To remedy this:• reduce the load by removing measurements,• reduce the screen brightness or stop the recorder.Internal temperature conditions can also cause the battery to not charge. This is necessary to protect the battery from damage and does not indicate a malfunction. Keep the monitor at room temperature and move it away from heat sources or out of direct sunlight. The battery will resume charging when the temperature is within range again. The battery will charge more quickly if the monitor is switched off.
4 FM20/30 Battery Option106Conditioning the BatteryYou must condition the battery when the "battery requires maintenance" symbol shows on the screen. Do not interrupt the charge or discharge cycle during conditioning.CAUTIONCondition the battery with a monitor not currently in use. The monitor switches off automatically when there is no battery power left.To condition the battery,1Charge the battery until it is completely full. Open the Battery Status window and check that the Batt fully charged message is displayed.2Disconnect the monitor from mains power, and let the monitor run until there is no battery power left and the monitor switches itself off.3Reconnect the monitor to mains power and charge the battery until it is full for use or charge to 50% for storage.Storing the BatteryThe battery should not remain inside the monitor if it is not used for a longer period of time. Batteries should be charged to a maximum of 50% for storage. For battery removal or exchange, contact your service personnel.NOTEThe battery will discharge over time in a monitor that is not connected to AC via the external power supply (M8023A). The reported values for "remaining capacity" and "runtime" will become less accurate when the battery is stored in this way for a longer period of time (that is, several weeks).
4 FM20/30 Battery Option107Battery Safety InformationWARNINGUse only Philips batteries part number M4605A. Use of a different battery may present a risk of fire or explosion.Do not open batteries, or dispose of them in fire, or cause them to short circuit. They may ignite, explode, leak or heat up, causing personal injury.If battery leakage should occur, avoid contact with skin. Refer to qualified and authorized service personnel.Dispose of used batteries promptly and in an environmentally-responsible manner. Do not dispose of the battery in normal waste containers. Consult your hospital administrator to find out about local arrangements. Do not expose batteries to liquids.Do not crush, drop or puncture batteries - mechanical abuse can lead to internal damage and internal short circuits which may not be visible externally.If a battery has been dropped or banged against a hard surface, whether damage is visible externally or not:• discontinue use• dispose of the battery in accordance with the disposal instructions above.Keep batteries out of the reach of children.CAUTIONDo not disassemble, heat above 100°C (212°F) or incinerate the batteries, to avoid the risk of fire and burns. Keep batteries out of the reach of children and in their original package until you are ready to use them.If battery leakage should occur, use caution in removing the battery. Avoid contact with skin. Refer to qualified and authorized service personnel.Do not install or use pre-damaged batteries.
4 FM20/30 Battery Option108
5 Alarms1095AlarmsThe alarm information here applies to all measurements. Measurement-specific alarm information is contained in the sections on individual measurements.The fetal monitor has two different types of alarm: patient alarms and INOPs.Patient AlarmsRed and yellow alarms are patient alarms. A red alarm indicates high priority, such as a potentially life threatening situation (for example, SpO2 below the desaturation alarm limit). A yellow alarm indicates a lower priority alarm (for example, a fetal heart rate alarm limit violation).INOPsINOPs are technical alarms. They indicate that the monitor cannot measure and therefore not detect critical conditions reliably. If an INOP interrupts monitoring and alarm detection (for example, MECG Leads Off), the monitor places a question mark in place of the measurement numeric and sounds an audible tone. INOPs without this tone indicate that there may be a problem with the reliability of the data, but that monitoring is not interrupted.Most INOPs are light blue, however there are a small number of INOPs which are always yellow or red to indicate a severity corresponding to red and yellow alarms. The following INOPs can also be configured as red or yellow INOPs to provide a severity indication:•MECG Leads Off•<SpO₂ Label> No Pulse•Tele Disconnected•Battery Empty / Replace BatteryAlarm DelaysThere is a delay between a physiological event at the measurement site and the corresponding alarm indication at the monitor. This delay has two components:•The general measurement delay time is the time between the occurrence of the physiological event and when this event is represented by the displayed numerical values. This delay depends on the algorithmic processing and, for certain measurements (SpO2, EEG and BIS), on the configured averaging time. The longer the averaging time is configured, the longer it takes until the numerical values reflect the physiological event.•The time between the displayed numerical values exceeding an alarm limit and the alarm indication on the monitor. This delay is the sum of the alarm delay configured for the specific measurement plus the system alarm delay. The system alarm delay is the processing time the system needs for any alarm on the monitor to be indicated after the measurement has triggered the alarm. See the performance specifications in “Specifications and Standards Compliance” on page 269 for the system alarm delay specification.Multiple AlarmsIf more than one alarm is active, the alarm messages are shown in the alarm status area in succession. An arrow symbol next to the alarm message informs you that more than one message is active.The monitor sounds an audible indicator for the highest priority alarm. If more than one alarm condition is active in the same measurement, the monitor announces the most severe.
5 Alarms110WARNINGAlarm systems of the monitor and those of the connected OB system are independent and not synchronized.Alarm ModeYou can configure the alarm mode for your fetal monitor. There are two possible modes:•All: alarms and INOPs are enabled, with all audible and visual indicators active.•INOP only: only INOPs are enabled, with audible and visual indication active. This is the default alarm mode.WARNINGIn INOP only mode, no fetal/maternal patient alarms are enabled or indicated.The alarm status area for yellow and red alarms shows the INOP only indication in conjunction with the "Alarms Off" symbol. No alarm limits or alarm off icons are displayed. No fetal/maternal patient alarm settings are available in the setup menus.Nurse Call SystemsIf configured to do so, red, yellow and light blue alarms are indicated on a nurse call system which is connected to the optional nurse call relay. Visual Alarm IndicatorsAlarm message: An alarm message appears in the alarm status area on the second line at the top of the screen indicating the source of the alarm. If more than one measurement is in an alarm condition, the message changes every two seconds, and has an arrow at the side. The background color of the alarm message matches the alarm priority: red for red alarms, yellow for yellow alarms, and light blue for INOPs. The asterisk symbols (*) beside the alarm message match the alarm priority: *** for red alarms, ** for yellow alarms. INOPs are displayed without asterisks.Depending on how your monitor is configured, it may display alarm limit violation messages:• in text form, for example ** FHR1 Low or• in numeric form, for example **FHR1 94<110, where the second number shows the currently set alarm limit, and the first number shows the value at which that alarm limit was violated by the widest margin.Flashing numeric: The numeric of the measurement in alarm flashes.Bright alarm limits: If the alarm was triggered by an alarm limit violation, the corresponding alarm limit on the monitor screen is shown more brightly.
5 Alarms111Audible Alarm IndicatorsThe audible alarm indicators configured for your fetal monitor depend on which alarm standard applies in your hospital. Audible alarm indicator patterns are repeated until you acknowledge the alarm by switching it off or pausing it, or until the alarm condition ceases (if audible alarm indication is set to non-latching).WARNINGDo not rely exclusively on the audible alarm system for fetal monitoring. Adjustment of alarm volume to a low level or off during monitoring may result in a dangerous situation. Remember that the most reliable method of fetal monitoring combines close personal surveillance with correct operation of monitoring equipment.Alarm Tone ConfigurationThe audible alarm indicators of your monitor are configurable. In the monitor's Configuration Mode, you can:• increase the alarm volume of unacknowledged alarms at regular intervals• change the interval between alarm sounds (ISO/IEC Standard alarms only)• change the base volume of the red and yellow alarm tones and the INOP tones• change the alarm sound to suit the different alarm standards valid in different countries.Standard Philips Alarms• Red alarms: a high pitched sound is repeated once a second.• Two-star yellow alarms and yellow INOPs: a lower pitched sound is repeated every two seconds.• One-star yellow alarms (short yellow alarms): the audible indicator is the same as for yellow alarms, but of shorter duration.• Standard INOPs: an INOP tone is repeated every two seconds.ISO/IEC Standard 9703-2 Audible Alarms• Red alarms and red INOPs: a high pitched tone is repeated five times, followed by a configurable pause.• Two-star yellow alarms and yellow INOPs: a lower pitched tone is repeated three times, followed by a configurable pause.• One-star yellow alarms (short yellow alarms): the audible indicator is the same as for yellow alarms, but of shorter duration.• Standard INOPs: a lower pitched tone is repeated twice, followed by a pause.
5 Alarms112Changing the Alarm Tone VolumeThe alarm volume symbol at the top right of the monitor screen gives you an indication of the current volume. To change the volume:1Select the volume symbol.2The volume scale pops up.3Select the required volume from the volume scale.When the alarm volume is set to zero (Off), the alarm volume symbol shows this symbol:If you switch the alarm volume off, you will not get any audible indication of alarm conditions.Minimum Volume for Severe Yellow or Red INOPsSevere yellow or red INOPs require action to ensure the well-being of the patient. Therefore the minimum volume for the INOP tone is set to at least alarm volume 8, irrespective of the current alarm volume setting. The INOP tone will sound even if the monitor alarm volume is set to zero.The severe INOPs for which this applies are:Alarm VolumeINOP Factory Default INOP toneBattery Empty cyan severe (fetal monitor with battery option)hard (CL Pods)soft (CL transducers)ECG Leads Off cyan hardNBP Cuff Overpress cyan severeCuff Not Deflated cyan severe!! <SpO₂ Label> No Pulse cyan hard
5 Alarms113Power Loss ToneFM20/30withBatteryOption,FM40/50When power is lost - no power is available from the AC power source or from the battery - a beeper will sound. The tone can be silenced by pressing the On/Standby button.Acknowledging AlarmsTo acknowledge all active alarms and INOPs, select the Silence key This switches off the audible alarm indicators.A check mark beside the alarm message indicates that the alarm has been acknowledged.If the condition that triggered the alarm is still present after the alarm has been acknowledged, the alarm message stays on the screen with a check mark symbol beside it.If the alarm condition is no longer present, all alarm indicators stop and the alarm is reset.Switching off the alarms for the measurement in alarm, or switching off the measurement itself, also stops alarm indication.Acknowledging Disconnect INOPsAcknowledging an INOP that results from a disconnected transducer switches off the associated measurement.Alarm ReminderIf Alarm Reminder is configured on for your monitor, you will get an audible reminder of alarm conditions that remain active after you have acknowledged the alarm. This reminder may take the form of a repetition of the alarm tone for a limited time, or an unlimited repetition of the alarm tone (this is the same as a new alarm). Alarm Reminder is available only for yellow and red INOPs and not for standard light blue INOPs.In Configuration Mode, you can set the interval between silencing the alarm and sounding the reminder tone to one, two, or three minutes.
5 Alarms114Pausing or Switching Off AlarmsIf you want to temporarily prevent alarms from sounding, for example while you are moving a patient, you can pause alarms. Depending on your fetal monitor configuration, alarms are paused for one, two, or three minutes, or infinitely.To view the alarm pause setting chosen for your unit:1Select Main Setup, Alarms, Alarm Settings.2Check the Alarms Off setting.This setting can be changed in Configuration Mode.There are some settings made in Configuration Mode that can affect the availability of the pause alarms functionality.•The Pause Alarms / Alarms Off permanent key can be removed from the screen to avoid unintentional switching off of alarms. In this case you can only pause alarms or switch alarms off permanently in the Alarms menu, under Main Setup.•The Pause Alarms / Alarms Off permanent key and the corresponding hardkey can be configured to pause or switch off red and yellow alarms, yellow alarms only, or not to function at all. If they are configured not to function, you cannot pause alarms or switch alarms off permanently at all.When the alarms off priority is set to Yellow Only, the Pause Alarms / Alarms Off key becomes the Pause Yellow / Yellow Al. Off.To Pause All AlarmsIf you have configured alarms to be paused for one, two, or three minutes, the SmartKey is labeled Pause Alarms.Select the Pause Alarms SmartKey to pause all alarms.Or1Select Main Setup.2Select Alarms.3Select Pause Alarms.To Switch All Alarms OffYou can switch alarms off permanently if your monitor is configured to allow infinite alarms pause, and the SmartKey is labeled Alarms Off.Select the Alarms Off SmartKey.Or1Select Main Setup.2Select Alarms.
5 Alarms1153Select Alarms Off.To Switch Individual Measurement Alarms On or OffThis applies to alarm mode All.1Select the measurement numeric to enter its setup menu.2Select Alarms to toggle between On and Off.The alarms off symbol is shown beside the measurement numeric.While Alarms are Paused or OffWhen red alarms are paused or off:The red Alarms Paused lamp on the monitor front panel is lit.In the alarm field, the monitor displays the message Al. Paused x:yy or Alarms Off, together with the alarms paused symbol or the alarms off symbol.When yellow alarms are paused or off:The yellow Alarms Paused lamp on the monitor front panel is lit.In the alarm field, the monitor displays the message YellowPaused x:yy or Yellow Alarms Off, together with the alarms paused symbol or the alarms off symbol.For red and yellow alarms:• No alarms are sounded and no alarm messages are shown.• INOP messages are shown but no INOP tones are sounded.The following INOPs are the only exceptions:NBP Cuff Overpress, Batt Empty and Batt Malfunction (these INOPs are issued even if alarms are paused or off).These INOPs switch the alarms on, and the INOP tones are sounded, even if alarms are paused or off. You need to remove the INOP condition first before you can switch the alarm tones off again.Restarting Paused AlarmsTo manually switch on alarm indication again after a pause, select the SmartKey Pause Alarms (or Alarms Off) again.Alarm indication starts again automatically after the pause period expires. If the monitor is configured to stay paused infinitely, you must select Alarms Off again to restart alarm indication. Alarms Paused Alarms Off
5 Alarms116Extending the Alarm Pause TimeIf your monitor has the function extended alarm pause enabled, you can extend the alarm pause time. Use this to prevent alarms being indicated, for example, while you are washing a patient or carrying out a procedure. Only extend the alarm pause time when you are sure that clinical personnel are available to monitor the patient's condition closely.To extend the alarm pause time to five or 10 minutes,1Select one of the alarm fields. This calls up the Alarm Messages window.2Select either the pop-up key PauseAl. 5 min or the pop-up key PauseAl. 10 min. Each time you select one of these pop-up keys, the Alarm Pause Time is reset to five (or 10) minutes.Alarm LimitsThe alarm limits you set determine the conditions that trigger yellow and red limit alarms.WARNINGBe aware that the monitors in your care area may each have different alarm settings, to suit different scenarios. Always check that the alarm settings are appropriate before you start monitoring.Viewing Individual Alarm Limits (Alarm Mode "All" Only)You can usually see the alarm limits set for each measurement next to the measurement numeric on the main screen. If your monitor is not configured to show the alarm limits next to the numeric, you can see them in the appropriate measurement setup menu. Select the measurement numeric to enter the menu and check the limits.Changing Alarm LimitsTo change individual measurement alarm limits using the measurement's setup menu:1In the measurement's setup menu, select the alarm limit you want to change. This calls up a list of available values for the alarm limit.2Select a value from the list to adjust the alarm limit.Alarm LimitsAudio source symbol
5117Reviewing AlarmsTo review the currently active alarms and INOPs, select any of the alarm status areas on the fetal monitor screen. The Alarm Messages window pops up. All alarms and INOPs are erased from the monitor's alarm history when you discharge a patient, or if you enter Demonstration Mode.Alarm Messages WindowThe Alarm Messages window shows all the currently active alarms and INOPs in chronological order, beginning at the top with the most recent. INOPs are shown on the left hand side, and alarms are shown on the right hand side. Any active red alarms are shown first, followed by yellow alarms. Acknowledged alarms or INOPs are shown with the check mark symbol.The Alarm Messages window pop-up keys appear when the window is opened. Selecting the Review Alarms pop-up key opens the Review Alarms window.Review Alarms WindowThe Review Alarms window contains a list of up to 300 of the most recent alarms and INOPs with date and time information. If configured to do so, each alarm is shown with the alarm limit active when the alarm was triggered and the maximum value measured beyond this limit. The Review Alarms window also shows any changes made to the Alarms On/Off or Silence status. Only the main alarms On/Off transitions are logged in the alarm history, and On/Off alarm transitions for individual measurements are not logged.The information in the Review Alarms window is deleted when a patient is discharged.The Review Alarms window pop-up keys appear when the window is opened. Selecting the Active Alarms pop-up key opens the Alarm Messages window.1Alarms On2SpO₂ No Pulse3Alarms Silenced4** FHR1 High5** SpO₂ Low
5 Alarms118Latching AlarmsThe alarm latching setting for your monitor defines how the alarm indicators behave when you do not acknowledge them. When alarms are set to non-latching, their indicators end when the alarm condition ends. Switching alarm latching on means that visual and/or audible alarm indications are still displayed or announced by the monitor after the alarm condition ends. The indication lasts until you acknowledge the alarm.Viewing the Alarm Latching SettingsTo see the alarm latching setting for your monitor:1In the monitor's Main Setup menu, select Alarms.2Select Alarm Settings, and see the Visual Latching and Audible Latching settings.This setting can be changed in Configuration Mode. You should be aware of the settings chosen for your unit. There are three possible choices each for visual and audible latching: Red, Red & Yellow, and Off. The audible latching configuration can never be configured to a higher level than that configured for the visual latching. In other words, the audible latching setting is always the same level, or lower, than the visual latching setting. For example, if visual latching is configured to Red Only, then audible latching can only be set to Red or Off. The following table shows the possible combinations for latching settings:Possible Combinations for Alarm Latching SettingsVisual Latching Setting Audible Latching SettingRed & Yellow Red & YellowRed & Yellow RedRed & Yellow OffRed RedRed OffOff Off
5 Alarms119Alarm Latching BehaviorAll INOPs except the "unplugged" INOPs are non-latching.Testing AlarmsIn general, to test the functioning of visible and audible alarms, do the following:1Enable the alarm.2Set the alarm limits.3Measure or simulate the parameter that is out of range, or signal loss.4Verify that the visible and audible alarms are working.As an example, to test the FHR alarms:1Connect the US transducer to a fetal sensor socket.2Enable the FHR alarming (see “Turning Alarms On or Off ” on page 185).Set the high alarm limit and delay to 150 bpm and 60 seconds respectively, and the low alarm limit and delay to 110 bpm and 60 seconds respectively (see “Changing Alarm Limits” on page 185).1Generate a fetal heart rate of approximately 180 bpm (3 beats per second) for more than one minute.2Verify the functioning of the visible and audible alarm.Alarm Condition Red and Yellow Measurement AlarmsAcknowledgment Presence Non-latching alarms Visual and audible latchingVisual latching, audible non-latchingAlarm has not been acknowledgedAlarm condition still presentAlarm tone on Alarm messageAlarm tone on Alarm message Flashing numericsAlarm tone on Alarm message Flashing numericsAlarm condition no longer presentAll audible and visual alarm indicators automatically stopAlarm tone onAlarm messageFlashing numericsAlarm message Flashing numericsAudible alarm indicators automatically stopAlarm has been acknowledgedAlarm condition still presentAlarm tone off. Alarm message. Audible alarm reminder (if configured)Alarm tone off Alarm message Flashing numerics Audible alarm reminder (if configured)Alarm tone off Alarm message Flashing numerics Audible alarm reminder (if configured)Alarm condition no longer presentAudible and visual alarm indicators automatically stopAudible and visual alarm indicators automatically stopAudible and visual alarm indicators automatically stop
5 Alarms120Alarm Behavior at Power OnIf the monitor is switched off for longer than one minute and then switched on again, or after a loss of power lasting longer than one minute, the monitor can be configured to restore either the alarm settings from the monitor's User Defaults, or the most recently used alarm settings. When a patient is discharged, the User Defaults of the monitor are always restored independent of the setting. After any of these situations, you should check that the alarm settings are appropriate for your patient. If power is lost for less than one minute, the alarm settings prior to the power loss are restored.If AlarmsOffAtStart is enabled in Configuration Mode alarms will be initially paused or off the next time the monitor is switched on (depending on the configuration setting for Alarms Off). Even if it is enabled, this setting only takes effect if the power down time is more than one minute, and the Global Setting Automat Default is set to Yes.In order for alarms to be paused or switched off initially:• the monitor must be switched off for more than one minute, and• the main alarms were switched off or paused before the monitor was switched off.
6 Patient Alarms and INOPs1216Patient Alarms and INOPsThis chapter lists alarms and technical alarms (INOPs) for the fetal monitors irrespective of their priority.Alarm MessagesFetal alarms are identified by either "FHR" or "DFHR". All other alarms without these identifiers refer to maternal parameters.Alarm Message From Condition Indication*** Brady (Pulse)***Brady xxx < yyySpO2The heart rate from the Pulse signal has fallen below the bradycardia limit. xxx denotes the lowest measured value; yyy is the bradycardia limit.Numeric flashes and alarm limit is highlighted, red alarm message, alarm tone.*** Desat*** Desat xx < yySpO2The SpO2 value has fallen below the desaturation alarm limit. xx denotes the lowest measured value, and yy is the desaturation limit.Numeric flashes, red alarm message, alarm tone.** DFHR1 High** DFHR2 High** DFHR3 High**DFHR1 xxx>yyy**DFHR2 xxx>yyy**DFHR3 xxx>yyyFHR (DECG) The fetal heart rate obtained from DECG has risen above the high alarm limit.xxx denotes the highest measured value, and yyy is the high alarm limit.Numeric flashes and high limit is highlighted, yellow alarm message, alarm tone.** DFHR1 Low** DFHR2 Low** DFHR3 Low**DFHR1 xxx<yyy**DFHR2 xxx<yyy**DFHR3 xxx<yyyFHR (DECG) The fetal heart rate obtained from DECG has fallen below the low alarm limit.xxx denotes the lowest measured value, and yyy is the low alarm limit.Numeric flashes and low limit is highlighted, yellow alarm message, alarm tone.*** Extreme Brady***Brady xxx < yyyMECG The maternal heart rate obtained from the maternal ECG has fallen below the extreme bradycardia limit.xxx denotes the lowest measured value, and yyy is the extreme bradycardia limit.Numeric flashes, red alarm message, alarm tone.
6 Patient Alarms and INOPs122*** Extreme Tachy***Tachy xxx > yyyMECG The maternal heart rate obtained from the maternal ECG has risen above the extreme tachycardia limit.xxx denotes the highest measured value, and yy is the extreme tachycardia limit.Numeric flashes, red alarm message, alarm tone.** FHR1 High** FHR2 High** FHR3 High**FHR1 xxx>yyy**FHR2 xxx>yyy**FHR3 xxx>yyyFHR (ultrasound) The fetal heart rate obtained from ultrasound has risen above the high alarm limit.xxx denotes the highest measured value, and yyy is the high alarm limit.Numeric flashes and high limit is highlighted, yellow alarm message, alarm tone.** FHR1 Low** FHR2 Low** FHR3 Low**FHR1 xxx<yyy**FHR2 xxx<yyy**FHR3 xxx<yyyFHR (ultrasound) The fetal heart rate obtained from ultrasound has fallen below the low alarm limit.xxx denotes the lowest measured value, and yyy is the low alarm limit.Numeric flashes and low limit is highlighted, yellow alarm message, alarm tone.** HR High**HR xxx>yyyMECG The maternal heart rate obtained from the maternal ECG has risen above the high alarm limit.xxx denotes the highest measured value, and yyy is the high alarm limit.Numeric flashes and high limit is highlighted, yellow alarm message, alarm tone.** HR Low**HR xxx<yyyMECG The maternal heart rate obtained from the maternal ECG has fallen below the low alarm limit.xxx denotes the lowest measured value, and yyy is the low alarm limit.Numeric flashes and low limit is highlighted, yellow alarm message, alarm tone.** NBPs High** NBPd High** NBPm HighNoninvasive blood pressureThe measured noninvasive blood pressure value is above the high alarm limit.s, d, or m after the label s indicates whether the systolic, diastolic or mean pressure has crossed the limit.Numeric flashes and high limit is highlighted, yellow alarm message, alarm tone.** NBPs Low** NBPd Low** NBPm LowNoninvasive blood pressureThe measured noninvasive blood pressure value is below the low alarm limit.s, d, or m after the label s indicates whether the systolic, diastolic or mean pressure has crossed the limit.Numeric flashes and low limit is highlighted, yellow alarm message, alarm tone.** Pulse High SpO2The pulse rate has exceeded the high alarm limit.Numeric flashes and high limit is highlighted, yellow alarm message, alarm tone.** Pulse Low SpO2The pulse rate has dropped below the low alarm limit.Numeric flashes and low limit is highlighted, yellow alarm message, alarm tone.Alarm Message From Condition Indication
6 Patient Alarms and INOPs123** SpO₂ High SpO2The arterial oxygen saturation has exceeded the high alarm limit.Numeric flashes and high limit is highlighted, yellow alarm message, alarm tone.** SpO₂ Low SpO2The arterial oxygen saturation has fallen below the low alarm limit.Numeric flashes and low limit is highlighted, yellow alarm message, alarm tone.*** Tachy (Pulse)***Tachy/P xxx>yyySpO2The heart rate from the Pulse signal has exceeded the tachycardia limit.xxx denotes the highest measured value, and yyy is the tachycardia limit.Numeric flashes, alarm limit is highlighted, red alarm message, alarm tone.** <iTemp Label> High iTemp The temperature value has exceeded the high alarm limit.Numeric flashes and high limit is high-lighted, yellow alarm lamp, alarm tone** <iTemp Label> Low iTemp The temperature value has dropped below the alarm limit.Numeric flashes and high limit is high-lighted, yellow alarm lamp, alarm toneAlarm Message From Condition Indication
6 Patient Alarms and INOPs124Technical Alarm Messages (INOPs)Monitor INOPsINOP Message Indication What to doBus Master Malfunc Monitor: INOP tone There is a problem with the monitor's hardware. Contact your service personnel.Bus Master Incomp Monitor: INOP tone The Bus Master board or firmware is incompatible and cannot be used with this monitor software revision. Contact your service personnel.Check Flex Texts Monitor: INOP tone If this INOP appears, check the monitor and patient settings before you resume monitoring. If the settings are unexpected, there may be a problem with the monitor software. Contact your service personnel.Check Monitor Func Monitor: INOP tone A potential internal problem with the monitor has been detected. Contact your service personnelCheck Keyboard Monitor: INOP tone Perform a visual and functional check of the keyboard. Contact your service personnel.Check Mouse Monitor: INOP tone Perform a visual and functional check of the mouse input device. Contact your service personnel.Check OBR Config Monitor: INOP tone OBR (OB Radio) channel configuration is invalid or settings are not present. Check channel configuration and hardware option.Check Settings Monitor: INOP tone If this INOP appears, check the monitor and patient settings before you resume monitoring. If the settings are unexpected, there may be a problem with the monitor software. Contact your service personnel.Check TI Config Monitor: INOP tone If this INOP appears, the monitor can be used normally, except for the Trace Interpretation feature. Contact your service personnel.Check Touch Input Monitor: Display only Perform a visual and functional check of the touch input device. Contact your service personnel.Coincidence Monitor: INOP tone One or more fetal/maternal heart rates/pulse rates persistently coincide with each other (see “Cross-Channel Verification (CCV)” on page 149). The INOP tone has a configurable delay. The default setting is an instant INOP tone.Internal.Comm.Malf Monitor: INOP tone There is a problem with I2C Bus communication in the monitor. Contact your service personnel.No Central Monit. Monitor: INOP tone There is a problem with the communication to the network. Central monitoring is currently not possible (no patient alarms or information). Check the connection. Contact your service personnel.Paper End Monitor: INOP tone The end of the paper pack is detected. Insert a new pack of paper.
6 Patient Alarms and INOPs125Settings Malfunct Monitor: INOP tone The monitor cannot use the predefined settings for monitoring. Contact your service personnel.Speaker Malfunct Monitor: INOP tone Contact your service personnel to check the speaker and the connection to the speaker.SRR Incompatible Monitor: INOP tone The connected SRR (Short Range Radio) board or FW cannot be used with this base station SW revision. Contact your service personnel.SRR Malfunction Monitor: INOP tone Malfunction in the SRR (Short Range Radio) module(s). If the INOP persists, contact your service personnel.SRR Invalid Chan Monitor: INOP tone The channel configuration of the Short Range Radio is invalid. Check channel and channel mask configuration.SRR Interference Monitor: INOP tone The short range radio connection has interference from another device. Try using another channel.Tele Malfunction Monitor: INOP tone Malfunction of the connected base station. If the INOP persists contact your service personnel.Tele Unsupported Monitor: INOP tone The base station is not supported by the monitor. Check software revisions.TimeExpired:NST Monitor: INOP tone(Message and tone only if Setup NST Timer, Notification is set to Alarm.The time has expired for the NST timer. Clearing the timer clears the INOP.Unsupported LAN Monitor: INOP tone There is a problem with the communication to the network and central monitoring is currently not possible. Check the connection. If the INOP persists, switch off the monitor and contact your service personnel.User I/F Malfunct Monitor: INOP tone Perform a visual and functional check of all the monitor input devices. Contact your service personnel.INOP Message Indication What to do
6 Patient Alarms and INOPs126FM20/FM30 Battery INOPsRecorder INOPsINOP Message Indication What to doBatt Empty Monitor: INOP toneBattery: battery LED flashes during this INOP, alarms cannot be paused or switched offThe estimated remaining battery-powered operating time is less than 10 minutes. Connect the monitor to AC immediately.If the condition persists and the monitor is not connected to mains power, this INOP is re-issued two minutes after you acknowledge it.Batt Incompat Monitor: INOP tone The battery cannot be used with this monitor. Replace it with the correct battery.Batt Low Monitor: INOP tone The estimated battery-powered operating time remaining is less than 20 minutes.Batt Malfunction Monitor: INOP toneBattery: battery LED flashes during this INOP, alarms cannot be paused or switched off unless the monitor is connected to mains power.The monitor cannot determine the battery status. If the INOP persists, replace the faulty battery. If the condition persists and the monitor is not connected to mains power, this INOP is reissued two minutes after you acknowledge it.Batt Missing Monitor: INOP tone No battery found in FM20/30. Contact your service personnel.Charger Malfunct Monitor: INOP toneBattery: battery LED may flashThere is a problem with the battery charger in the monitor. Connect the monitor to mains power and contact your service personnel.Check Batt Temp Monitor: INOP tone The temperature of the battery is too high. Check that the monitor is not exposed to heat.INOP Message Indication What to doCheck Paper Monitor: display onlyRecorder: Print-outCheck that there is no paper jam, that the print drawer is properly shut, that the paper is loaded with the grid facing upwards, and that the correct Philips paper is being used.FetRec Equip Malf Monitor: INOP tone There is a problem with the fetal recorder hardware. Contact your service personnel.FetRec Chk Config Monitor: INOP tone Recorder Speed and/or Scale Type settings are set to "Unknown" and need to be set to the correct values in Configuration Mode before the recorder can be operated.Printhead Overheat Monitor: INOP tone The printhead is too hot. The recorder stops, the recorder Start/ Stop key is disabled, and remains so until the printhead cools down sufficiently. Wait for the printhead to cool down, then press the recorder Start/ Stop key or the Silence key to clear the INOP.
6 Patient Alarms and INOPs127Wired Transducer INOPsFHR (Ultrasound)IUPTocoWrong Paper Scale Monitor: INOP toneRecorder: Print-outThe grid scale of the paper in the monitor does not match the grid scale configured in the monitor. Make sure that you use the correct paper and scale for your institution:pre-printed: 30-240 in US and Canada, 50-210 in other geographies.INOP Message Indication What to doINOP Message Indication What to doFHR1 Equip MalfFHR2 Equip MalfFHR3 Equip MalfMonitor: INOP tone There is a problem with the FHR hardware. Contact your service personnel.FHR1 Signal LossFHR2 Signal LossFHR3 Signal LossMonitor: INOP toneINOP tone if Alarm Mode is set to ALL. No tone if Alarm Mode is set to INOP only.The input signal quality is not sufficient to process the measurement. Adjust the position of the transducer to obtain a better signal.FHR1 UnpluggedFHR2 UnpluggedFHR3 UnpluggedMonitor: INOP tone Reconnect the FHR transducer to the monitor. Check all connections are sound.INOP Message Indication What to doIUP Equip Malf Monitor: INOP tone There is a problem with the IUP hardware. Contact your service personnel.IUP Unplugged Monitor: INOP tone Reconnect the IUP transducer to the monitor. Check all connections are sound.INOP Message Indication What to doToco Equip Malf Monitor: INOP tone There is a problem with the Toco hardware. Contact your service personnel.Toco Unplugged Monitor: INOP tone Reconnect the Toco transducer to the monitor. Check all connections are sound.Pulse(Toco) Malf Monitor: INOP toneToco MP Maternal Pulse MeasurementThere is a problem with the Toco MP transducer hardware. Contact your service personnel.
6 Patient Alarms and INOPs128Cableless Transducer INOPsINOP Message Indication What to docl US Disconnectcl Toco Disconnectcl ECG/IUP DisconnMonitor: INOP tone CL transducer: tone and cyan LEDThe cableless transducer has lost the connection to the monitor for more than 5 sec.cl US Malfunctioncl Toco Malfcl ECG/IUP MalfMonitor: INOP tone Numeric is replaced by a -?-CL transducer: tone and cyan LEDMalfunction of the transducercl US Batt Lowcl Toco Batt Lowcl ECG/IUP BattLowMonitor: Display onlyCL transducer: LED flashes redThe remaining monitoring time with this transducer is below 30 minutes. Charge battery.cl US Batt Empty!!cl US Batt Empty!!!cl US BattEmptycl Toco Batt Empty!!clToco BattEmpty!!!clTocoBattEmptycl ECG/IUP Empty!!cl ECG/IUP Empty!!!clECG/IUP EmptyMonitor: Display onlyCL transducer: LED flashes redThe remaining monitoring time with this transducer is below 15 minutes. Charge battery.cl US Batt Malfcl Toco Batt MalfclECG/IUP BattMalfMonitor: INOP tone CL transducer: tone and cyan LEDMalfunction of the battery system (charger circuit or battery) detected (e.g. persistent communication error, over-voltage, over-current, battery incompatible). Contact your service personnel.cl US Check Tempcl Toco Chk TempclECG/IUP Chk TempMonitor: INOP tone CL transducer: tone and cyan LEDThe temperature of the transducer or its battery is critically high. If the transducer is docked on the base station, charging is interrupted. Check that device is not covered and do not expose device to heat sources. Do not place the base station in a sunny window in a room without active air conditioning. The environment temperature to charge a transducer battery should not exceed 40 °C. If the INOP persists, remove device from patient and contact your service personnel.
6 Patient Alarms and INOPs129DECG and MECG INOPsNBP INOPsINOP Message Indication What to doDFHR1 Equip MalfDFHR2 Equip MalfDFHR3 Equip MalfMonitor: INOP tone There is a problem with the DECG hardware. Contact your service personnel.DFHR1 Leads OffDFHR2 Leads OffDFHR3 Leads OffMonitor: INOP toneNumeric is replaced by a -?-One or more DECG lead is not attached. Make sure that all required leads are attached, and no electrodes have been displaced. Check all connections are sound, and that the legplate attachment electrode is properly attached. If the INOP persists, try using another adapter cable, or legplate attachment electrode. If the INOP persists, contact your service personnel.DFHR1 Signal LossDFHR2 Signal LossDFHR3 Signal LossMonitor: INOP toneNumeric is replaced by a -?-INOP tone if Alarm us set to ALL. no tone if Alarm Mode is set to INOP only. The input signal quality is not sufficient to process the measurement. Reapply the fetal scalp electrode.DFHR1 UnpluggedDFHR2 UnpluggedDFHR3 UnpluggedMonitor: INOP toneNumeric is replaced by a -?-Reconnect the DECG transducer to the monitor. Check all connections are sound.MECG Equip Malf Monitor: INOP tone There is a problem with the MECG hardware. Contact your service personnel.MECG Leads Off Monitor: INOP toneNumeric is replaced by a -?-One or more MECG lead is not attached. Ensure that all required leads are attached, and no electrodes have been displaced. Check all connections are sound. If the INOP persists, try using another adapter cable. If the INOP still persists, contact your service personnel. MECG Unplugged Monitor: INOP toneNumeric is replaced by a -?-Reconnect the MECG transducer to the monitor. Check all connections are sound.INOP Message Indication What to doCuff Not Deflated Monitor: INOP tone (severe yellow/red INOP tone)Numeric is replaced by a -?-During this INOP, alarms cannot be paused or switched off.Remove the cuff from the patient. Make sure that the tubing is not kinked or twisted. Try restarting the measurement. You can silence the INOP, but the INOP message remains visible until the next measurement is started or the Stop All SmartKey is selected.
6 Patient Alarms and INOPs130NBP Cuff Overpress Monitor: INOP tone (severe yellow/red INOP tone)Numeric is replaced by a -?-During this INOP, alarms cannot be paused or switched off.The cuff pressure exceeds the overpressure safety limits. Remove the cuff from the patient. Ensure that the tubing is not kinked or twisted and that the correct patient category is selected. Try restarting the measurement. You can silence this INOP, but the INOP message remains visible until the next measurement is started or the Stop All SmartKey is selected.NBP Equip Malf Monitor: INOP toneNumeric is replaced by a -?-Remove the cuff from the patient. The noninvasive blood pressure hardware is faulty. Contact your service personnel. You can silence this INOP, but the INOP message remains visible until the next measurement is started or the Stop All SmartKey is selected.NBP Interrupted Monitor: INOP toneNumeric is replaced by a -?-Check the tubing and cuff for leakages or kinks. Check that you are using the correct cuff size and placement, and that the correct patient category is selected. Try restarting the measurement. If the INOP occurs repeatedly, contact your service personnel.You can silence this INOP, but the INOP message remains visible until the next measurement is started or the Stop All SmartKey is selected. This INOP arises when the measurement needed longer than the maximum time for inflation, deflation or the total measurement.NBP Measure Failed Monitor: INOP toneNumeric is replaced by a -?-Check that you are using the correct cuff size and placement, and that the correct patient category is selected. Try restarting the measurement.You can silence this INOP, but the INOP message remains visible until the next measurement is started or the Stop All SmartKey is selected.Check the condition and suitability of the patient for noninvasive blood pressure monitoring. Use another cuff to continue measuring.INOP Message Indication What to do
6131CL NBP Pod INOPsINOP Message Indication What to docl NBP Disconnect Monitor: INOP toneCL NBP Pod: INOP tone and display messageThe CL NBP Pod has lost the SRR connection to the monitor.cl NBP No Cradle Monitor: INOP toneCL NBP Pod: display messageThe CL NBP Pod is not in the cradle. You can silence this INOP, but the INOP message remains visible until the CL NBP Pod is inserted into the cradle and the next measurement is started or the Stop All SmartKey is selected.cl NBP Remove Monitor: INOP toneCL NBP Pod: display messageThe temperature of the battery in the CL NBP Pod is too high. Remove the Cableless Measurement Device from the patient and contact service personnel.cl NBP Batt Empty!!cl NBP BattEmpty!!!cl NBP BatEmptyMonitor: INOP toneCL NBP Pod: display messageThe remaining battery time of the CL NBP Pod is below 30 minutes. Charge the battery.cl NBP Batt Incomp Monitor: INOP toneCL NBP Pod: display messageThe battery in use with the CL NBP Pod is incompatible. Replace it with one approved for use with the CL NBP Pod.cl NBP Batt Low Monitor: INOP toneCL NBP POD: display messageThe remaining battery time of the CL NBP Pod is below 2 hours.cl NBP Batt Malf Monitor: INOP toneCL NBP Pod: display messageThere is a malfunction in the CL NBP Pod's battery system. Contact your service personnel.cl NBP Batt Temp Monitor: INOP toneCL NBP Pod: display messageThe temperature of the battery in the CL NBP Pod is critically high. Check that the Pod is not covered or exposed to a heat source. If the INOP persists, remove the Pod from the patient and contact your service personnel.cl NBP Check Batt Monitor: INOP toneCL NBP Pod: display messageThe battery in the CL NBP Pod is nearing the end of its useful life. Only 50 charge/discharge cycles remain. Contact your service personnel to replace the battery.cl NBP Serv Batt Monitor: INOP toneCL NBP Pod: display messageThe battery in the CL NBP Pod has reached the end of its useful life. It can no longer be charged. Contact your service personnel to replace the battery.
6 Patient Alarms and INOPs132SpO2 INOPsINOP Message Indication What to doSpO₂ Equip Malf Monitor: INOP tone There is a problem with the SpO2 hardware. Contact your service personnel.SpO₂ Erratic Monitor: INOP toneNumeric is replaced by a -?-Check the sensor placement. Try another adapter cable and sensor. If the INOP persists, contact your service personnel.SpO₂ Extd.Update Monitor: display onlyNumeric is replaced by a -?-The update period of displayed values is extended due to a noninvasive blood pressure measurement on the same limb or an excessively noisy signal.SpO₂Interference Monitor: INOP toneNumeric is replaced by a -?-There is too much interference, caused by a high level of ambient light and/or electrical interference. Cover the sensor to minimize ambient light. If the INOP persists, ensure that the sensor cable is not damaged or positioned too close to power cables.SpO₂ Low Perf Monitor: display onlyNumeric is replaced by a -?-Accuracy may be compromised due to very low perfusion. Stimulate circulation at sensor site. If INOP persists, change the measurement site.SpO₂ NoisySignal Monitor: INOP toneNumeric is replaced by a -?-Excessive patient movement or electrical interference is causing irregular pulse patterns. Try to reduce patient movement or to relieve the cable strain on the sensor.SpO₂ No Pulse Monitor: INOP toneNumeric is replaced by a -?-Check the perfusion at measurement site. If necessary, stimulate circulation or change measurement site. If the INOP is due to noninvasive blood pressure measurement on the same limb, wait until the measurement is finished.SpO₂ No Sensor Monitor: INOP toneNumeric is replaced by a -?-Ensure the SpO2 sensor is connected. If the INOP persists, try another adapter cable and sensor. If you silence this INOP, the measurement will be switched off.SpO₂ Poor Signal Monitor: display onlyNumeric is replaced by a -?-The signal condition of the SpO2 measurement is poor and measurement accuracy may be compromised.SpO₂ Pulse? Monitor: INOP toneNumeric is replaced by a -?-The detectable pulsations of the SpO2 signal are outside the specified pulse rate range.SpO₂ Searching Monitor: display onlyNumeric unavailableSpO2 is analyzing the patient signal to derive Pulse, and SpO2 values. Please wait until the search analysis is complete.SpO₂ Sensor Malf Monitor: INOP toneNumeric unavailableThe SpO2 sensor or adapter cable is faulty. Try another adapter cable and sensor. If the INOP persists, contact your service personnel.SpO₂ Sensor Off Monitor: INOP toneNumeric unavailableThe SpO2 sensor is not properly applied to the patient. Apply the sensor following the instructions supplied by the manufacturer.SpO₂ Unkn.Sensor Monitor: display onlyNumeric is replaced by a -?-The connected sensor or adapter cable is not supported by the SpO2 measurement. Use only specified sensors and cables.
6 Patient Alarms and INOPs133CL SpO2 Pod INOPsSpO₂ Upgrade Monitor: display onlyNumeric unavailableThe SpO2 measurement is currently in UPGRADE mode. Monitoring is not possible in this mode.INOP Message Indication What to doINOP Message Indication What to docl SpO₂ Batt Empty!!cl SpO₂ BatEmpty!!!cl SpO₂ BtEmptyMonitor: INOP toneCL SpO2 Pod: display messageThe remaining battery time of the CL SpO2 Pod is below 30 minutes. Charge the battery.cl SpO₂ Batt Incmp Monitor: INOP toneCL SpO2 Pod: display messageThe battery in use with the CL SpO2 Pod is incompatible. Replace it with one approved for use with the CL SpO2 Pod.cl SpO₂ Batt Low Monitor: INOP toneCL SpO2 Pod: display messageThe remaining battery time of the CL SpO2 Pod is below 2 hours.cl SpO₂ Batt Malf Monitor: INOP toneCL SpO2 Pod: display messageThere is a malfunction in the CL SpO2 Pod's battery system. Contact your service personnel.cl SpO₂ Batt Temp Monitor: INOP toneCL SpO2 Pod: display messageThe temperature of the battery in the CL SpO2 Pod is critically high. Check that the Pod is not covered or exposed to a heat source. If the INOP persists, remove the Pod from the patient and contact your service personnel.cl SpO₂ Check Batt Monitor: INOP toneCL SpO2 Pod: display messageThe battery in the CL SpO2 Pod is nearing the end of its useful life. Only 50 charge/discharge cycles remain. Contact your service personnel to replace the battery.cl SpO₂ Serv Batt Monitor: INOP toneCL SpO2 Pod: display messageThe battery in the CL SpO2 Pod has reached the end of its useful life. It can no longer be charged. Contact your service personnel to replace the battery.cl SpO₂ Disconnect Monitor: INOP toneCL SpO2 Pod: INOP tone and display messageThe CL SpO2 Pod has lost the SRR connection to the monitor.cl SpO₂ No Cradle Monitor: INOP toneCL SpO2 Pod: display messageThe CL SpO2 Pod is not in its cradle.cl SpO₂ Remove Monitor: INOP toneCL SpO2 Pod: display messageThe temperature of the battery in the SpO2 Pod is too high. Remove the SpO2 Pod from the patient and contact service personnel.
6 Patient Alarms and INOPs134Tympanic Temperature INOPsINOP Message Indication What to do<iTemp Label> MalfunctionMonitor: INOP toneNumeric is replaced by a -?-The thermometer or the interface board are defective. Check module on another monitor. Connect another module to this monitor and replace the interface board. If the problem persists, contact your service personnel.<iTemp Label> Incompat.Monitor: INOP toneNumeric is replaced by a -?-The iTemp device firmware is not supported by the monitor software.<iTemp Label> Meas FailedMonitor: INOP toneNumeric is replaced by a -?-Ambient temperature is out of range. If ambient temperature is within valid range, check the thermometer. Try to end the stand-by mode by picking up a new probe cover. If the problem persists, replace thermometer and contact your service personnel.<iTemp Lbl> NO DEVICE Monitor: INOP toneNumeric unavailableThe thermometer is not connected to the monitor.<iTemp Label> OverrangeMonitor: INOP toneNumeric is replaced by a -?-Temperature measurement is out of range. If temperature of measurement is within valid range, check with another thermometer.
71357Admitting and DischargingThe fetal monitor can store basic patient demographic information used to identify patients.Admit/Discharge on the MonitorThis section describes how you admit and discharge patients when using the monitor as a stand-alone device (that is, when not used with an obstetrical information and surveillance system such as OB TraceVue/IntelliSpace Perinatal).Admitting a PatientThe fetal monitor displays physiological data as soon as a patient is connected. This lets you monitor a patient who is not yet admitted. It is however important to admit patients properly so that you can identify your patient on recordings.Use the Patient Demographics window and its associated pop-up keys to admit and discharge patients.To admit a patient,1Select the patient name field or select the Patient Demogr. SmartKey to open the Patient Demographics window.2Clear any previous patient data by selecting Dischrge Patient and then Confirm.If you do not discharge the previous patient, you will not be able to distinguish data from the previous and current patients, for example, on the recording.3Select Admit Patient.4Enter the patient information: select each field and use the on-screen keyboard.If a conventional keyboard is connected to the monitor you can use this to enter patient information:–Last Name: Enter the patient's last name (family name), for example Doe.–First Name: Enter the patient's first name, for example Jane.–MRN: Enter the patient's medical record number (MRN), for example 12345678. Depending on your configuration this field may be labeled differently e.g. "Record ID", "Lifetime Id", "Account Number", "Serial Number", or "SSN".–Gestational Age: Enter the gestational age of the pregnancy. Enter one numeric for the week (0-50) and one numeric for the day (0-6).–Date of Birth: Enter the patient's date of birth.
7 Admitting and Discharging1365Select Confirm. The patient status changes to admitted. If the recorder is running, the recorder stops and immediately restarts to annotate the new patient data.Quick Admitting a PatientUse Quick Admit to quickly admit a patient using only a limited set of demographic data.1Select the Quick Admit SmartKey.2Enter the required data (ID fields or last name depending on configuration) with the keyboard or a barcode scanner.3Select Enter.4In the confirmation window, select Confirm to stop monitoring for the previous patient or free up the fetal monitor (if confirmation is configured).5If the monitor is connected to an Information Center and only the ID field is entered, the patient name may be set to - - - at the Information Center, depending on the configuration.Complete the rest of the demographic details as soon as possible to fully identify the patient on the network, on the monitor, and on printed reports. To complete the details, open the Patient Demographics window and complete all required fields.Editing Patient InformationTo edit the patient information after a patient has been admitted, select the patient name field on the main screen of the fetal monitor to open the Patient Demographics window, and enter the required changes.Discharging a PatientYou should always perform a discharge even if your previous patient was not admitted. A discharge:– clears the information in the Patient Demographics window.– resets all monitor settings to the settings defined in the User Default.– advances the paper automatically if the recorder is running.– stops the fetal recorder.When a patient is discharged from the monitor, all patient demographic data is deleted (trace data is not affected).Depending on your configuration, monitoring for a patient may end automatically when the fetal monitor has been powered off or in standby mode for a set time.To discharge a patient,1Select the patient name field to display the Patient Demographics window and associated pop-up keys.2Select the pop-up key for Dischrge Patient.3Select Confirm to discharge the patient.CAUTIONIn order to ensure that the settings are reset to user defaults for a new patient, always discharge the previous patient from the fetal monitor.
7 Admitting and Discharging137NOTEIn order to ensure a continuous record, it is recommended to discharge the patient at the monitor before performing a new patient admission in OB TraceVue/IntelliSpace Perinatal.New Patient CheckThe fetal monitor can be configured to ask you in certain situations:• after a specified power-off period• after a specified standby periodwhether a new patient is now being monitored. The pop-up window is entitled Is this a New Patient? The monitor offers a Yes key to discharge the previous patient and begin monitoring a new patient, and a No key to continue monitoring with the current patient data and settings.The time periods for the two conditions can be configured independently.OB TraceVue/IntelliSpace PerinatalWhen the monitor is connected to an OB TraceVue/IntelliSpace Perinatal system over a LAN connection, the OB TraceVue/IntelliSpace Perinatal system acts as the "master" over patient demographic data. All patient and location-related data that is visible on the monitor is set, overwritten or updated by the OB TraceVue/IntelliSpace Perinatal system. See the OB TraceVue/IntelliSpace Perinatal Instructions for Use for details.Transferring a PatientWhen you are transferring a patient from one bed to another, both the monitor from which you are transferring her and the monitor to which you are transferring her must be switched on and connected to the OB TraceVue/IntelliSpace Perinatal network during the patient transfer. OB TraceVue/IntelliSpace Perinatal via RS232In contrast to a LAN connection, when the monitor is connected to an OB TraceVue/IntelliSpace Perinatal system over an RS232 connection, the OB TraceVue/IntelliSpace Perinatal system has no control over the monitor's patient admission and discharge functions.Depending on how OB TraceVue/IntelliSpace Perinatal is configured, either the Last Name, First Name and the bed label, or just the bed label alone, are taken from the OB TraceVue/IntelliSpace Perinatal system. See the OB TraceVue/IntelliSpace Perinatal Instructions for Use for details.
7 Admitting and Discharging138
81398Non-Stress Test TimerThe non-stress test (NST) timer shows the elapsed time for the non-stress test. The timer counts up to the time you set for the NST.Setting NST Autostart/AutostopYou can set the recorder so that it starts automatically (NST Autostart) when the NST timer is started, and stops automatically (NST Autostop) when the NST is complete (when the set run time has elapsed). As default, NST Autostart is On, and NST Autostop is Off.Viewing the NST TimerYou can configure the timer notification symbol, (the NST label), a progress bar and the elapsed time to be displayed in the top left-hand corner of the screen. By default, the NST timer is not displayed on the screen.Alternatively, you can view the timer in the Timers window.To open the Timers window:Eithera. Press the Timer SmartKey.Orb. Access the NST pop-up keys (see “Accessing the NST Setup Pop-up Keys” on page 140), and press the Timers key.
8 Non-Stress Test Timer140Timer Expiry NotificationWhen the timer expires, the color changes from blue to green, you hear a single tone, and a message appears in the status line on the main screen.The volume of the tone can be set in Configuration Mode.Accessing the NST Setup Pop-up KeysYou control and set up the NST timer (for example, start, stop, or clear the timer, and set the run time) using a selection of pop-up keys that you access via any one of three possible routes:•Via the Timer SmartKey (Route 1).•Via the Main Setup SmartKey (Route 2).• Via the NST menu entry in the menu that pops-up when you touch the top left-hand corner of the screen (Route 3).Via the Timer SmartKey (Route 1)♦Press the Timer SmartKey. The Timers window opens, and the pop-up keys for controlling/setting up the NST timer appear (see “Pop-up Keys for NST Timer Setup” on page 141).Via the Main Setup SmartKey (Route 2)1Enter the Main Setup menu using the SmartKey.2Select NST to enter the Setup NST menu. At the same time, the pop-up keys for setting up the NST timer appear (see “Pop-up Keys for NST Timer Setup” on page 141).Via the NST Field (Route 3)♦Select the NST field displayed in the top left-hand corner of the screen (when so configured). The pop-up keys for controlling/setting up the NST timer appear (see “Pop-up Keys for NST Timer Setup” on page 141).
8 Non-Stress Test Timer141Pop-up Keys for NST Timer SetupRun TimeThe run time can be set from 10 to 60 minutes. To set the run time, you first need to enter the Setup NST menu:1To enter the Setup NST menu:EitherEnter the Main Setup menu using the SmartKey. Then select NST.OrAccess the NST pop-up keys (see “Accessing the NST Setup Pop-up Keys” on page 140), and press the Setup NST key.2Select Run Time.Pop-Up Keys Selecting this pop-up key lets you.... CommentsStart Start the timer.Stop Stop the timer, allowing either restarting after a pause (Start) or clearing (Clear key).Setup NST Enter the Setup NST menu. From here you can set the run time.This pop-up key is not available with Route 2, as the Setup NST menu is already open.Timer Return to the Timers window. This pop-up key is not available with Route 1, as the Timers window is already open.
8 Non-Stress Test Timer142
9 Non-Stress Test Report1439Non-Stress Test ReportIt is generally accepted that a non stress test (NST) allows you to assess fetal well-being. The monitor's NST report process uses fetal ultrasound (but not DECG) heart rate traces and the Maternal Toco trace, generating a printed report when criteria are met and it is an indication of the fetal well-being. The American term Non Stress Test (NST) is used for antepartum testing. The interpretation algorithm and rule set are equivalent to those implemented in OB TraceVue Revision G.xx or IntelliSpace Perinatal H.xx and higher, and are based on the 2008 NICHD guidelines.An NST report is a diagnostic aid, but it does not replace the clinician’s judgment. The interpretation and the appropriate clinical response remain with the clinician.A fetus normally produces characteristic heart rate patterns. Average baseline variability and acceleration of the FHR in response to fetal movement are considered reassuring signs. This test does not take into account any form of external fetal stimulation.For every active ultrasound fetal heart rate measurement, one NST report can reside in the monitor’s memory. The reports are cleared when you discharge a patient and when you start a new NST report.When the NST Report option is available and the "NST Report" feature is "on", the NST status for all available ultrasound fetal heart rate measurements are displayed on the screen.The minimum displayed information is:• NST identification (by FHR number: 1, 2, 3)• Current NST status (by color: inverse for "not started yet", white for "running", yellow for "stopped", green for "finished")Setting Up an NST ReportTo setup NST Report functionality:1Enter the Main Setup menu and select the NST Report or2Select the NST Report SmartKey.3Press the "Setup" pop-up key.4Set your configuration options.Select from:•NST Analysis. Choose from On or Off.This switches the report feature on or off. This is linked to the NST timer. Both must be set to On for the NST report to function.•Report Recording. Choose from:–Manual - press the Record Report pop up key to trigger a manual request.–After Recorder Stop - report is recorded as soon as recorder becomes idle.–Immediately - If a realtime recording is running, the monitor pauses it. The recording is continued after the report has been recorded.Average short term variability (STV) value is documented in [bpm] and [ms] if STV is configured as part of the NST Report. This parameter is not considered as reassuring criteria.
9 Non-Stress Test Report144NST Report Status WindowThe NST Report window displays a detailed overview of the current NST status for any available ultrasound fetal heart rate measurement. You can see:• NST Status - whether it is ready, ongoing, or the time and date at which it was stopped, or at which it finished.• Elapsed time - the time that has elapsed since the NST began.• Accelerations - the number of FHR accelerations detected so far.• Baseline - the average baseline value.• Variability - the average variability value.• Short Term Variability - the current short term variability (STV) value.• Decelerations - the number of FHR decelerations detected so far.• FHR Availability - current statistical FHR availability value.• Sinusoidal - the current status of sinusoidal rhythm detection.For criteria not yet met, a white arrow symbol marks the overall status on the top line, and also appear against every criterion not yet met. A yellow symbol indicates detection of severe or prolonged decelerations.The pop-up keys let you perform the following actions:•FHR1, FHR2, FHR3 - switch to the window showing the current NST status for the fetal heart rate.•Record Report - print the NST Report on paper.•Record Trace - record the trace episode that belongs to the current report. Depending on device usage, the trace recording might be incomplete.•Setup - open the Setup NST Report window.
9145Example NST ReportField Field ContentReport Title, with FHR label and dateNST Report for FHR1 on 12 Oct. 2009Product Information Product DE53102345 G.01.70, OB A.04.24,Toco DE52401090, FHR1 DE00002345 A.05.26Patient Information Rogers, AliceAge: 27Gestational Age: Week 34, Day 5Start time, end time, Elapsed time, configured Run time Time: 11:34 - 12:06Elapsed time:32 minutesRun time: 20 minutesOverall one-line NST result summaryNST Criteria*: not metTitle Trace Interpretation SummaryResult Accelerations Accelerations: 2at: 11:59 12:02Result: Contractions Contractions: 3at: 11:57 12:00 12:04Result: Baseline and VariabilityBaseline: 125 bpm (Range: 118 bpm - 129 bpm)Variability: 23 bpm (Range: 20 bpm - 24 bpm)Short Term Var.: 0.9 bpm (3.8 msec)Statistics: FHR availabilityFHR available: 95%Result: Decelerations Decelerations: 1at: 11:58severeprolonged
9 Non-Stress Test Report146NST CriteriaThe patient is monitored for a user-definable period of time (10 - 60 minutes in steps of 5 minutes). The test is considered reassuring when the following criteria are met:• The fetal heart rate is valid at least 90% (this is configurable) of the specified time span.• The FHR features a user-defined minimum number of accelerations.• The FHR features a user-defined maximum number of tolerated decelerations, and does not include severe or prolonged decelerations, which are never tolerated.• The average baseline fetal heart rate lies within the user-defined limits for low heart rate and high heart rate over the whole time span.• The FHR exhibits a moderate variability (user-defined) for the specified time span.Result:Sinusoidal Rhythm detectedSinusoidal: NoResult: Decelerations before Reporting PeriodEvents before Reporting Period:Decelerations: 1at: 11:38severeprolongedThis field is enabled if there were decelerations between the start of NST and the start of the reporting period.Guideline / Criteria Information(*) Interpretation Criteria based on guideline "NICHD 2008, v01"User-defined criteria for CTG tracing:• valid FHR for 90% of reporting period• baseline heart rate between 120 and 160 bpm• at least 2 accelerations in 10 min• not more than 1 decelerations• moderate baseline variability (5 - 25 bpm)• short term var. greater than 5.0 msecAdditional Criteria:• no severe or prolonged decelerations• no sinusoidal pattern in reporting periodField Field Content
9 Non-Stress Test Report147An NST Report is generated when the reassuring criteria are met the first time in the current monitoring phase. When performing NST with twins or triplets, a separate NST Report is generated for each fetus.In the printed report, the average short term variability (STV) value is shown in bpm and ms. This is not part of the reassurance criteria.After the reassurance criteria have been met, the clinician can print the NST Report and then turn the fetal monitor off, or may continue fetal monitoring and print the report at any time.Non-Reassuring ReportIf the reassurance criteria are not met when the test has run for 90 minutes, or if you stop anytime during the 90 minute period, then the test is stopped, and a report is generated stating the reassurance criteria have not been met.Non-Reactive NST TestIf a non-reactive test occurs and you then use acoustic stimulation, you must exercise caution in interpreting the resulting traces, as artificial stimulation is not taken into account when calculating test results.
9 Non-Stress Test Report148
10 Cross-Channel Verification (CCV)14910Cross-Channel Verification (CCV)Misidentification of Heart RatesFHR detection by the monitor may not always indicate that the fetus is alive. Confirm fetal life before monitoring, and continue to confirm that the fetus is the signal source for the recorded fetal heart rate (see “Confirm Fetal Life Before Using the Monitor” on page 10).To reduce the possibility of mistaking the maternal HR or pulse for FHR, or FHR1 for FHR2 or FHR3, it is recommended that you monitor both maternal HR/pulse and the heart rates of all fetuses (see “Monitoring FHR and FMP Using Ultrasound” on page 155, “Monitoring Twin FHRs” on page 171, “Monitoring Triple FHRs” on page 179, and “Monitoring Maternal Heart / Pulse Rate” on page 223). Here are some examples where the MHR can be misidentified as the FHR, or one FHR for another FHR (twins/triplets).•When using an ultrasound transducer:– It is possible to pick up maternal signal sources, such as the maternal heart, aorta, or other large vessels. Especially if the recorded MHR, and any other artifact is over 100 bpm.– It is possible to pick up the same fetal heart rate simultaneously with multiple transducersNOTEWhen an ultrasound transducer is connected to the monitor, but not applied to the patient, the measurement may generate unexpected intermittent FHR readings.•When Fetal Movement Profile (FMP) is enabled:The FMP annotations on a fetal trace alone may not always indicate that the fetus is alive. For example, FMP annotations in the absence of fetal life may be a result of:– Movement of the deceased fetus during or following maternal movement.– Movement of the deceased fetus during or following manual palpation of fetal position (especially if the pressure applied is too forceful).– Movement of the ultrasound transducer.•When using a scalp electrode (DECG):– Electrical impulses from the maternal heart can sometimes be transmitted to the fetal monitor through a recently deceased fetus via the spiral scalp electrode, appearing to be a fetal signal source.
10 Cross-Channel Verification (CCV)150Cross-Channel Verification FunctionalityThe cross-channel verification functionality (CCV) of the fetal monitors compares all monitored heart rates (maternal and fetal), and indicates automatically whether any two channels are picking up the same signal, or monitoring similar values.If the fetal monitor detects that any channels have the same or similar values the Coincidence INOP is issued with an INOP tone that can have a configurable delay. In addition yellow questions marks appear next to the numerics on the touch screen that have the same or similar values. On the recording trace there is also a question mark printed out from the point where recorded traces continuously overlap.Visual Aids for CCV DetectionOverview of Cross-Channel ComparisonsMeasurements from TransducersMeasurement Comparison Done by the Fetal Monitor for Cross-Channel VerificationCoincidence INOP appears on the touch screen of the fetal monitor.Question mark next to the numerics that show the same or similar values appears on the touch screen of the fetal monitor.Question mark printed out on the recorder trace from the point where two measured values coincide.Measurement TransducerFHR US From Ultrasound or CL Ultrasound transducerDFHR (DECG) From a fetal scalp electrodeMaternal pulse From Toco MP, or CL Toco+MP transducerMaternal pulse From SpO2 or CL SpO2 PodMaternal heart rate From MECG electrodesFHR1 (US) FHR2 (US) FHR3 (US) DFHR (DECG)FHR1 (US)FHR2 (US)FHR3 (US)
10151DFHR (DECG)Maternal Pulse (Toco MP)Maternal Pulse (SpO2)Maternal HR (MECG)FHR1 (US) FHR2 (US) FHR3 (US) DFHR (DECG)
10152Coincidence ExamplesCoincidence of Maternal Pulse and FHRWhen the maternal pulse and FHR are being monitored, and the measured values are very similar or the same, the coincidence question mark is displayed on the monitor’s screen above both of the corresponding numerics (in this case maternal pulse and FHR). Often the signal loss or coincidence happens because the fetal or maternal movement displaced the ultrasound transducer, and a repositioning of the transducer is necessary.1Coincidence INOP2Coincidence question mark by FHR13Coincidence question mark by pulse from Toco MP
10 Cross-Channel Verification (CCV)153The coincidence question mark is also printed on the trace paper next to the corresponding FHR and maternal pulse.Coincidence of Twins/Triplets FHRsWhen both FHR1 and FHR2 are being monitored, and the measured values are very similar or the same, the coincidence question mark is displayed on the monitor’s screen above both of the corresponding numerics (in this case FHR1 and FHR2).1Printed coincidence question mark on trace2FHR1 and pulse traces1Coincidence INOP2Coincidence question mark by FHR13Coincidence question mark by FHR2
10 Cross-Channel Verification (CCV)154The coincidence question mark is also printed on the trace paper next to the corresponding FHR1 and FHR2.Recommended Actions for INOP Coincidence1Confirm fetal life by palpation of fetal movement or auscultation of fetal heart sounds using a fetoscope, stethoscope, or Pinard stethoscope.2Manual determination of the maternal pulse and comparison with the fetal heart rate sound signals from the loudspeaker.3Reposition the transducer, or ensure that the fetal scalp electrode is placed correctly, until you receive a clear signal and the monitor is no longer issuing the Coincidence INOP.4In case of difficulties deriving a stable maternal pulse reading using the Toco MP or CL Toco+MP transducer, use SpO2 or the CL SpO2 Pod instead. In case of similar problems with the pulse measurement from SpO2, use MECG instead. Reasons to switch the method for deriving a maternal pulse or heart rate include: motion artifacts, arrhythmia, and individual differences in pulse signal quality on the abdominal skin (via Toco MP).5If you cannot hear the fetal heart sounds, and you cannot confirm fetal movement by palpation, confirm fetal life using obstetric ultrasonography.1Printed coincidence question mark on trace2FHR1 and FHR2 traces
11 Monitoring FHR and FMP Using Ultrasound15511Monitoring FHR and FMP Using UltrasoundTo monitor a single FHR externally, you use an ultrasound transducer attached to a belt around the mother's abdomen. The ultrasound transducer directs a low-energy ultrasound beam towards the fetal heart and detects the reflected signal. Your monitor can also detect fetal movements and print the fetal movement profile (FMP) on the trace. Monitoring using ultrasound is recommended from the 25th week of gestation for non-stress testing or routine fetal monitoring.WARNINGPerforming ultrasound imaging or Doppler flow measurements together with ultrasound fetal monitoring may cause false FHR readings, and the trace recording may deteriorate.Technical DescriptionFetal monitors use the ultrasound Doppler method for externally monitoring the fetal heart rate. Using the Doppler method, the transducer (in transmitter mode) sends sound waves into the body which are then reflected by different tissues. These reflections (Doppler echoes) are picked up by the transducer (in listening mode). These Doppler echoes are amplified and sent to the monitor’s speaker through which the fetal heart signal can be heard. In parallel the Doppler echoes are processed through an auto correlation algorithm to determine the fetal heart rate (FHR). The FHR is displayed on the monitor’s numeric display and on the recorded trace.Properly representing the fetal heart rate using a device that derives heartbeats from motion is a formidable task and the limitations of the technology will be discussed shortly. Basic fetal cardiac physiology may contribute to difficulties in obtaining a reliable ultrasound signal.A heart rate pattern of a fetus is capable of extraordinary variation, ranging from a stable pattern with minimal variation while the fetus is “asleep” to robust accelerations of 40-60 bpm above baseline rate over a few seconds, or exaggerated variability when the fetus is active. Decelerations of the rate 60-80 bpm below baseline may develop even more abruptly than the accelerations. The Beat-to-Beat arrhythmias of the FHR may further exaggerate how much the the FHR variability at the bottom of the variable decelerations, or in the presence of fetal breathing movements, which also tend to lower the fetal heart rate. The recognition of these normal variations in fetal heart rate patterns will greatly assist in the separation of genuine fetal information from the artifact.Limitations of the TechnologyAll tissues moving towards or away from the transducer generate Doppler echoes. Therefore, the resulting signal that is provided to the monitor’s speaker, and for further fetal heart signal processing, can contain components of the beating fetal heart wall or valves, fetal movements, fetal breathing or hiccup, maternal movements such as breathing or position changes, and pulsating maternal arteries.The fetal heart signal processing uses an auto correlation algorithm to obtain periodic events such as heart beats. If the signal is erratic such as from a fetal arrhythmia, the ultrasound device may have
11 Monitoring FHR and FMP Using Ultrasound156trouble tracking the abrupt changes, and may misrepresent the true FHR pattern. Signals such as those from moving fetal limbs are usually very strong, thereby masking the fetal heart signal. During prolonged movements where the fetal heart signal is masked, the FHR appears blank on the numeric display and as a gap on the recorded trace. Fetal position changes, maternal position changes, or uterine contractions can move the fetal heart partly or fully out of the ultrasound beam resulting in signal loss, or even picking up Doppler echoes from pulsating maternal arteries. In these cases a maternal heart rate or sometimes even a rate resulting from the mixture of fetal and maternal signals may be displayed on the monitor’s numeric display and on the recorded trace.In contrast to the timely well-defined R-peak of an ECG signal obtained with a fetal scalp electrode, the ultrasound Doppler signal from a fetal heart consists of multiple components from atria (diastole), ventricles (systole), valves, and pulsating arteries. These components vary depending on fetal and transducer position and angle, and are further modulated by factors such as fetal or maternal breathing. These effects may produce what is called “artifact”. Optimal transducer positioning therefore is key to minimizing these effects and thereby minimizing artifact.Misidentification of MHR as FHRFHR detection by the monitor may not always indicate that the fetus is alive. Confirm fetal life before monitoring, and continue to confirm that the fetus is the signal source for the recorded heart rate (see “Confirm Fetal Life Before Using the Monitor” on page 10 and “Cross-Channel Verification (CCV)” on page 149).What You Need• Ultrasound transducer• Toco MP or CL Toco+MP transducer•Ultrasound gel• Transducer belt (and optional butterfly belt clip, if applicable)Cableless Monitoring - Important ConsiderationsWhen using an Avalon CL or Avalon CTS Fetal Transducer system with your monitor, note the following:Refer to “Telemetry” on page 93 for general rules regarding the use of cableless transducers from an Avalon CL or Avalon CTS Cableless Fetal Transducer system.• When using a cableless ultrasound transducer from an Avalon CL or Avalon CTS system to measure the fetal heart rate, note that you cannot use any other ultrasound transducer (whether cableless or wired) at the same time.CAUTION Never use ultrasound transducers connected to more than one fetal monitor on the same patient.• When using an Avalon CL or Avalon CTS you should be aware that FMP is not recommended when the mother is likely to move, and you should disable Fetal Movement Profile (FMP) on the fetal monitor (Fetal Movement Off) if the mother is walking. See also “Fetal Movement Profile” on page 160.
11 Monitoring FHR and FMP Using Ultrasound157• With the Avalon CL Transducer System you can now monitor twins and triplets with cableless transducers. The Avalon CTS System does not have this option.The wireless symbol appears next to the measurement label, indicating that the measurement is being made by a cableless transducer.WARNING• Ensure that the conductive parts of the fetal scalp electrode and the maternal leg plate electrode do not contact other conductive parts, including earth.• Indication of the heart-rate may be adversely affected by the operation of cardiac pacemaker pulses or by cardiac arrhythmias.• During ambulant FHR monitoring, the chance of losing the signal or detecting the maternal heart rate is higher than during stationary monitoring. The frequency of the patient's walk may be detected, and mistaken for a FHR signal.• Check the mother’s pulse periodically during monitoring and compare this with the FHR signal. Beware of mistaking a “doubled” maternal heart rate for FHR. If a fetus is dead, there is a risk that the maternal heart rate is monitored and misinterpreted as the fetal heart rate. Therefore, the simultaneous monitoring of maternal heart rate (preferably, the maternal ECG) and the fetal heart rate is encouraged.• Do not interpret maternal movements as fetal movements.• Artifacts: FMP artifacts are generated during fetal heart rate searching by changing the transducer position, therefore Philips fetal monitors enable the FMP only after detecting a valid heart rate signal for several seconds. FMP is not recommended when the mother is likely to move, and you should disable Fetal Movement Profile (FMP) at the fetal monitor (Fetal Movement Off) if the mother is walking.• Gaps in maternal heart rate detection can occur:– if the transducer is not correctly positioned.– due to the pulsation of uterine blood vessels.–if the fetus moves.1FHR12Toco parameter
11 Monitoring FHR and FMP Using Ultrasound158Preparing to MonitorPrepare for ultrasound monitoring using the list below. The standard procedures in use in your facility determine the sequence of actions.1Determine fetal position.2Fasten the belt around the patient.3Switch on the monitor and the recorder.4Connect the transducer to a free socket. The signal quality indicator for the heart rate initially displays an invalid signal.5Apply a thin layer of ultrasound gel to the underside of the transducer.CAUTIONUsing ultrasound gel not approved by Philips may reduce signal quality and may damage the transducer. This type of damage is not covered by warranty.1Place the transducer on the abdomen, if possible over the fetal back or below the level of the umbilicus in a full-term pregnancy of cephalic presentation, or above the level of the umbilicus in a full-term pregnancy of breech presentation. Work the transducer in a circular motion to ensure the gel layer makes good contact.2When the sensor is connected correctly and you receive a good signal, the signal quality indicator should be filled out. If an inadequate signal is produced, the signal quality indicator will indicate a poor signal, and no numeric will appear on the screen.3Adjust the audio volume of the monitor's loudspeaker to a clearly audible level, while moving the transducer over the abdomen. When you have a good signal, secure the transducer in position below the belt.WARNINGPeriodically compare the mother's pulse with the signal coming from the monitor's loudspeaker to ensure that you are monitoring fetal heart rate. Do not mistake a doubled or elevated MHR for FHR.The ultrasound transducer may warm slightly (less than 1°C/1.8°F above ambient temperature) when applied to the patient,. When not applied, the transducer can reach a maximum temperature of 44°C/112.2°F at an air temperature of 40°C/104°F.Selecting Fetal Heart SoundYou can listen to the fetal heart sound from one ultrasound transducer at a time. When the fetal heart sound is selected for an FHR channel, you see the audio source symbol next to the FHR numeric label for that channel.
11 Monitoring FHR and FMP Using Ultrasound159To select the audio source for an FHR channel:1Enter the Setup FHR1 menu for the channel you want to hear (FHR1 used as an example).2Press Select Audio. It may take a few seconds for the audio source symbol to appear.Changing the Fetal Heart Sound VolumeThe FHR volume symbol at the top right of the Fetal Heart Sound Volume window gives you an indication of the current volume. To change the volume:1Select the volume symbol. The volume scale pops up.2Select the required volume from the volume scale.1FHR12Audio source symbol1Fetal Heart Sound Volume
11 Monitoring FHR and FMP Using Ultrasound160Fetal Movement ProfileThe Fetal Movement Profile (FMP) parameter detects fetal movements via an ultrasound transducer connected to the monitor. Only the fetus monitored on the FHR1 channel is monitored for FMP.Once you have enabled FMP (see “Switching FMP On and Off” on page 161), it is triggered automatically whenever:• You connect an ultrasound transducer.• A patient is discharged.When FMP is enabled, the ultrasound transducer detects most fetal body movements. Eye movements are not detected and movement of the feet and hands may not be detected. Positioning or repositioning of the transducer is recorded as fetal movement. Maternal movement, excessive fetal breathing, or fetal hiccups may also be recorded as fetal movement (also in case of fetal demise or during the second stage of labor). You can mark these artifacts on the trace paper using either the remote event marker, or the event marker key as described in “Marking an Event” on page 79. FMP should be interpreted with care, or disabled when the patient is ambulating or during 2nd stage of labor. Ignore these movements when you interpret the FMP. When monitoring twins or triplets, only the fetus monitored on the FHR1 channel is monitored for movement, but be aware that movements recorded for FHR1 may also be caused by movement of the second or third fetus.The fetal movement profile (FMP) appears as "activity blocks" (see A below) along the top of the Toco Scale, the length of each block showing the duration of the activity.FMP StatisticsFMP statistics are printed every ten minutes.1FMP enabled
11 Monitoring FHR and FMP Using Ultrasound161The FMP detection activates after about half a minute of steady heart rate signals (signal indicator half-full, or full) to minimize transducer positioning artifact. You will notice this deliberate delay:• When a new patient is admitted. A patient discharge restarts the FMP statistics from zero.• When you connect an ultrasound transducer.Switching FMP On and OffYou can switch FMP on and off from any FHR channel. For example, to set it from the FHR1 channel:1Enter the Setup FHR1 menu.2Select Fetal Movement to toggle between On and Off.3Return to the main screen.2FMP started hereAIndication of current fetal movement.BThe FMP statistics are presented as two percentage figures:The first figure shows the percentage of detected fetal movements in the previous ten minutes.CThe second figure shows the percentage of detected fetal movements since the start of recording.To mark the start of the FMP statistic, FMP is printed on the paper with an arrow.
11 Monitoring FHR and FMP Using Ultrasound162TroubleshootingProblem Possible Causes SolutionsErratic traceErratic displayFetal arrhythmia Consider monitoring FHR using DECG after the rupture of membranes.Obese patientTransducer position not optimal Reposition transducer until signal quality indicator shows a good signal (at least half-full).Belt loose Tighten beltToo much gel Remove excessVery active fetus -Insufficient gel Use enough gel to ensure the transducer makes good contact with the mother's skin.Signal quality indicator is continuously poorTransducer position not optimal Reposition transducer until signal quality indicator shows a good signal (at least half-full).FHR less than 50 bpm (and the FHR is audible)If membranes are ruptured, using a fetal scalp electrode (FM30 and FM50 only) allows measurement of FHR down to 30 bpm.Questionable FHR Recording MHR by mistake Reposition transducer.Confirm fetal life.Recording periodic signals when the transducer is not applied to the patientDisconnect all NON-USED ultrasound transducers, as continuous, regular mechanical, or electromagnetic influences can result in an artificial trace.Recorded FHR appears to be suspiciously higher, or suspiciously lower, than real FHR. In very rare cases, half- or double-counting of the FHR can occur.If you have reason to question the validity of the recorded FHR, always verify FHR by independent means (by auscultation, for example). Measure maternal pulse by independent means.FHR not recorded FHR is less than 50 bpm or over 240 bpm If membranes are ruptured, using a fetal scalp electrode (FM30 and FM50 only) allows measurement of FHR down to 30 bpm.If FHR is outside of the specified range, verify FHR by independent means.FHR1 Equip Malf or FHR2 Equip Malf or FHR3 Equip Malf INOP displayed.See “Patient Alarms and INOPs” on page 121.FHR1 Signal Loss or FHR2 Signal Loss or FHR3 Signal Loss INOP displayed.FHR1 Unplugged or FHR2 Unplugged or FHR3 Unplugged INOP displayed.If you suspect the transducer is malfunctioning Test the transducer.
11 Monitoring FHR and FMP Using Ultrasound163Additional InformationArtifact in Fetal Heart Rate MeasurementHow to detect it and reduce its occurrence using the Avalon Fetal MonitorThe ultrasound derived FHR measurement technique in Avalon fetal monitors, like all other ultrasound fetal monitors’ FHR measurement techniques, has limitations that can lead to misrepresentation of the fetal heart rate pattern and potential misinterpretation of the fetal condition.An incorrect interpretation of the trace may lead to either unnecessary interventions, or to failure to detect fetal distress and the need for intervention. Thus, the on-going evaluation of the recorded trace requires regular confirmation that the trace represents the true FHR. Specific situations requiring such confirmation include the following:• After starting a measurement or changing a transducer• After maternal position changes, for example during pushing with contractions• When the tracing shows abrupt changes in baseline rate, variability, or pattern (decelerations to accelerations) especially in the second stage of labor• When the baseline maternal heart rate is within about 15 bpm of the FHR• When the user is unable to determine a baseline rate and variability occurs between consecutive contractionsThere are several ways to verify the source and/or accuracy of the recorded fetal heart rate pattern. These include:Verification of the FHR with:• An obstetric stethoscope,• Ultrasound imaging, or• A fetal scalp electrodeVerification of the maternal heart rate:• Using pulse oximetry - for a maternal heart rate pattern displayed simultaneously with the FHR (Cross-Channel Verification (CCV) feature),• Using Maternal ECG - for a maternal heart rate pattern displayed simultaneously with the FHR (CCV feature), or• Manual determination of the maternal pulseWhenever possible measure the maternal pulse rate to make use of the monitor’s Cross-Channel Verification (CCV) feature, especially during the second stage of labor, or when the maternal pulse is elevated over 100 bpm. The Philips Avalon fetal monitor provides a Toco MP or CL Toco+MP transducer for maternal pulse detection and the creation of a maternal heart rate pattern plotted on the same recorder as the FHR pattern. In case of difficulties deriving a stable maternal pulse reading using the Toco MP or CL Toco+MP transducer, use SpO2 or MECG instead. When either of these parameters is utilized, the monitor will automatically and continuously perform a CCV of the maternal heart rate pattern against the FHR pattern displayed on the monitor. If the patterns and rates are similar, the CCV provides an alarm that both rates are probably from the same source (i.e., they both represent the maternal heart rate pattern and the fetus is not being monitored). Repositioning the ultrasound transducer will usually correct this, but it may be necessary to apply a fetal scalp electrode. Advising the mother to temporarily cease pushing during contractions may help to more rapidly resolve any uncertainty in this situation.
11 Monitoring FHR and FMP Using Ultrasound164Doubling: The auto correlation algorithm can display a doubled fetal or maternal heart rate if the duration of diastole and systole are similar to each other, and if the heart rate is below 120 bpm. Doubling, usually brief, is accompanied by an abrupt switch of the trace to double the baseline value.Halving: With fetal tachycardia (above 180 bpm) and some interference from breathing or maternal arteries the auto correlation algorithm may only recognize every second beat resulting in a halved rate for a limited time. If the actual FHR is above the maximum limit of the monitor (240 bpm), the algorithm will also half-count. Halving is accompanied by an abrupt switch of the trace to exactly half the prior baseline value. This switch may simulate a FHR deceleration and be referred to by clinicians as a “false deceleration.”Switching to maternal heart rate (also referred to as "Maternal Insertion"): The fetal heart can move partly or fully out of the ultrasound beam and the auto correlation algorithm may then pick up and display the maternal heart rate. Depending on the signal mix in the ultrasound signal, switching to the maternal heart rate may mimic several conditions with the potential for erroneous interpretation and response as follows:•The switch to the maternal heart rate may simulate a FHR deceleration (i.e., a decrease of the fetal heart rate, and be referred to by clinicians as a “false deceleration”).•The maternal heart rate may simulate a normal fetal heart rate pattern (i.e., it may mask a FHR deceleration or fetal demise).Especially during pushing with contractions in the second stage of labor, the maternal heart rate may increase to the point where it may equal or exceed the fetal rate. Here the maternal trace may mimic a normal fetal trace while the fetus may be having decelerations or fetal demise has occurred. This change from fetal to maternal heart rate pattern may not be at all obvious unless CCV is used and represents the most dangerous pitfall of all the artifacts because fetal distress may go unrecognized.•The maternal heart rate may simulate a FHR acceleration, which is an increase of the fetal heart rate.During expulsive efforts, the maternal heart rate normally accelerates and may be at or above the normal FHR range.•The FHR may display gradual appearing decelerations. Generally, the “false decelerations” described above are abrupt. Rarely, combinations of “noisy/erratic signal” associated with changes in maternal and/or fetal rate or movement will produce more gradual appearing “false decelerations” but these are usually short-lived with an abrupt return to an obviously stable FHR baseline.“Noisy/Erratic” signals: With mixed or weak signals the tracing may reveal very brief episodes of erratic recorded traces. These represent the auto correlation algorithm finding brief sequences of apparent and persistent heartbeats amidst a mixed or weak signal. These erratic recorded traces are commonplace, especially in association with fetal or maternal movement. During prolonged periods of such noisy/erratic signals, the fetus is not being adequately monitored.Drop out: With mixed or weak signals there may be no heart rate tracing at all. These episodes reflect that if the algorithm does not find an apparent and persistent heartbeat amidst a mixed or weak signal, it will not print a heart rate on the tracing. Brief episodes of drop out are commonplace, especially in association with fetal or maternal movement. During prolonged periods of drop out, the fetus is not being adequately monitored.
11 Monitoring FHR and FMP Using Ultrasound165Multiple FetusesWith multiple fetuses, the potential to experience these artifacts is increased. Positioning of the transducer is even more critical. Ultrasound scanning should be used to help with positioning of individual transducers. See also “Monitoring Twin FHRs” on page 171 and “Monitoring Triple FHRs” on page 179.Obtaining a Good Heart SignalTo successfully position the ultrasound transducer, first determine the fetal position using palpation. Position the transducer over the strongest audible fetal heart sound from the monitor’s speaker and wait at least six seconds after each transducer adjustment to verify a good signal quality displayed on the Signal Quality Indicator and a consistent FHR numeric display. Having determined the position that provides a strong fetal signal, fix the transducer on the abdomen with the belt.If the quality of the signal or the appearance of the heart rate trace from the ultrasound transducer is questionable, the transducer should be repositioned as described above. Alternatively, the use of an ultrasound scanner will greatly facilitate the determination of the optimal site for the ultrasound heart rate transducer. Factors during the second stage of labor that may influence the quality of the FHR tracing obtained with ultrasound include:• Uterine contractions• Changing contour of the maternal abdomen• Maternal body movement - positioning• Maternal expulsive efforts - pushing• Maternal tachycardia/accelerations with contractions• Fetal decelerations, Fetal tachycardia• Delayed return of the fetal heart rate from a deceleration• Descent of the fetus in the birth canal• Rotation of the fetus in the birth canalIn some cases during the second stage of labor, a good and reliable ultrasound FHR signal may not be obtainable, and the use of a fetal scalp electrode must be considered (fetal ECG).Heart Rate SoundThe heart rate sound emitted by the device is a representation of movement that, in most cases, permits accurate auscultation of the FHR corresponding to the FHR displayed on the monitor and rate pattern depicted on the trace recording. On occasion, the user may hear a FHR that differs from the FHR display and the recorded trace. This may occur in situations where the fetal heart moves partly out of the transducer ultrasound beam. In these cases, the user may hear the FHR emitted from the monitor’s speaker, even though another periodic signal (usually the maternal heart rate) has become stronger. The auto correlation algorithm will display the stronger maternal heart rate, despite the persistence of a weaker fetal signal. These occurrences are usually very brief and, if persistent, can be addressed by repositioning the transducer.
11 Monitoring FHR and FMP Using Ultrasound166Signal Quality IndicatorAvalon compared with its predecessor, the Series 50Signal quality indicator on Avalon fetal monitors:Instead of a traffic light-like design (red – yellow – green) used on the Series 50, the signal quality on the Avalon fetal monitor is indicated by a triangle on the touch screen that is displayed in one of three ways:Examples of ArtifactsWhen monitoring the maternal ECG, a beat-to-beat maternal heart rate trace is printed alongside the FHR recorded trace. When monitoring the maternal SpO2 derived pulse rate, a filtered and averaged heart rate trace is printed.Following are recorded trace examples of complaints received regarding inaccurate output from the Avalon monitors. Scaling is 3 cm/min and 30 bpm/cm.Avalon fetal monitor signal quality indicator display:1Completely filled triangle, indicating good signal quality (good/full).2Half-filled triangle, indicating limited signal quality. This condition may indicate a weak or ambiguous signal. If this status persists, reposition the transducer (acceptable/medium).3Empty triangle, indicating insufficient signal quality. No FHR is displayed on the monitor’s numeric display or the recorded trace. If this status persists, reposition the transducer (poor/no signal).Double-CountingBaseline Rate 120Baseline Variability ModerateAccelerations PresentDecelerations Not apparent
11 Monitoring FHR and FMP Using Ultrasound167Contractions Excessive, coupling, hypertonusArtifact Double-CountingComment Reassuring tracing. The excessive uterine activity should prompt discontinuation of any oxytocic agent.Remediation The true fetal rate can be confirmed by auscultation or by fetal scalp electrode.Double-CountingHalf-CountingBaseline Rate 120Baseline Variability ModerateAccelerations PresentDecelerations Not apparentContractions MinimalArtifact Half-counting, noise, drop outComment Reassuring tracing. The half-count at 4-5 minutes into the tracing may simulate a fetal deceleration, but the abruptness and the lack of any compensatory changes when the normal rate returns suggests that this is half-counting. Insertion of the maternal heart rate (see below) may produce a similar pattern. Note also very brief episodes of half-counting, maternal insertion, and signal drop out.Remediation Auscultation or the application of a direct scalp electrode, if feasible, will reveal the true fetal heart rate.Maternal-Switching (Maternal Insertion)
11 Monitoring FHR and FMP Using Ultrasound168Selection of Literature References on Artifacts___________________________________________________________Fetal Monitoring, A Multidisciplinary Approach, Seventh editionSusan M. Tucker, Lisa A. Miller, David A. MillerMosby Inc. 2009, ISBN 978-0-323-08352-2___________________________________________________________Baseline Rate 170 - TachycardiaBaseline Variability ModerateAccelerations Unable to determineDecelerations AbsentContractions AbsentArtifact Maternal insertion, noiseComment The fetus has an elevated baseline rate of about 170 bpm with minimal to moderate variability. The ability to assess fetal status is limited because about half of the tracing displays the maternal heart rate.Remediation The application of a maternal transducer (ECG or pulse oximeter) will likely resolve any possible confusion with the tracing. Repositioning the transducer may produce a more reliable tracing. Consideration must also be given to applying a fetal scalp electrode.Maternal-Switching (Maternal Insertion)Noisy/Erratic Signal and DropoutBaseline Rate 140Baseline Variability ModerateAccelerations PresentDecelerations AbsentContractions MinimalArtifact Noisy signal, drop-outComment Reassuring tracing. Note that there is episodic drop out of the signal with discontinuity of the fetal tracing.Remediation Either improving the position of the transducer or the application of a fetal scalp electrode will reduce the amount of artifact in the tracing.
11169Signal ambiguity resulting in unexpected outcome with external fetal heart rate monitoringBy Duncan R. Neilson Jr, MD; Roger K. Freeman, MD; Shelora Mangan, RNC, MSN, CNSAmerican Journal of Obstetrics & Gynecology, June 2008:___________________________________________________________Antepartal and Intrapartal Fetal Monitoring, 3rd Edition (2007)By Michelle L. Murray, PhD, RNCSpringer Publishing Company, ISBN 0-8261-3262-6Page 2, Table 2: Limitations of Continuous EFMItem 15: “The US may detect maternal aortic wall movement and the MHR will be printed. A failureto recognize the lack of a FHR may delay appropriate management.”Page 38, “Solving Equipment Problems”, Table 3: The Ultrasound Transducer___________________________________________________________JOGC (Journal of Obstetrics and Gynaecology Canada)Volume 29, Number 9, September 2007Chapter 2: Intrapartum SurveillancePage S35: “Methods of Electronic Fetal Monitoring”“… Among its disadvantages are the need for readjustment with maternal or fetal movements and thefollowing: the transducer may record the maternal pulse, it may be difficult to obtain a clear tracing inobese women or those with polyhydramnios, artifact may be recorded, and there may be doubling orhalving of the fetal heart rate when it is outside of the normal range.”___________________________________________________________Maternal of Fetal Heart Rate? Avoiding Intrapartum Misidentificationby Michelle L. MurrayJOGNN Clinical Issues, April 2003, 33, 93-104; 2004. DOI: 10.1177/0884217503261161Figure 9 "The recording is of the MHR with occasional doubling."___________________________________________________________Maternal Heart Rate Pattern – A Confounding Factor In Intrapartum Fetal SurveillanceSchifrin BS, Harwell R, Hamilton-Rubinstein T, Visser G:Prenat Neonat Med 2001; 6:75-82.___________________________________________________________Fetal Monitoring in Practice, 2nd Edition 1998
11 Monitoring FHR and FMP Using Ultrasound170By Donald Gibb, S. ArulkumaranButterworth-Heinemann, ISBN 0-7506-3432-2Page 65, “False or erroneous baseline because of double counting of low baseline FHR”Page 66, “Bradycardia: fetal or maternal”___________________________________________________________Role of Maternal Artifact in Fetal Heart Rate Pattern InterpretationKlapholz, Henry M, MD; Schifrin, Barry S. MD; Myrick, Richard RSObstetrics & Gynecology, September 1974, Volume 44, Issue 3___________________________________________________________Testing Ultrasound TransducersIf any of the following tests fail, repeat the test using another transducer. If the second transducer passes the tests, confirming that the first transducer is defective, contact your service personnel.If the second transducer also fails the tests, contact your service personnel.You can test all ultrasound transducers, including the cableless ones as described above.To test an ultrasound transducer:1Switch on the monitor and the recorder.2Connect the transducer to the fetal monitor.3Select the fetal heart sound for this channel.4Increase the loudspeaker volume to an audible level.5Holding the transducer in one hand, move your other hand repeatedly towards and then away from the surface.6Check that a noise is heard from the loudspeaker.
12 Monitoring Twin FHRs17112Monitoring Twin FHRsThe FHRs of twins are externally monitored using two ultrasound transducers. The Avalon CL Transducer system provides the option to monitor twins with cableless transducers. The Avalon CTS system does not have this option.FM30/50 Twin FHRs are monitored throughout labor and delivery. After rupture of the membranes, you can monitor one twin externally using ultrasound, and the other internally using DECG.Refer to the appropriate preceding chapters for contraindications, and more information about the available measurement methods.FHR detection by the monitor does not always indicate that the fetuses are alive. Confirm fetal life before monitoring, and continue to confirm that the fetuses are the signal source for the recorded fetal heart rates. See “Confirm Fetal Life Before Using the Monitor” on page 10 and “Cross-Channel Verification (CCV)” on page 149.Important ConsiderationsWhen monitoring:• Ensure that you are recording two different fetal heart rates. The cross-channel verification feature alerts you if the two heart rates coincide (if both transducers are recording the same FHR). If this happens, check the trace and if necessary, reposition an ultrasound transducer to detect the second FHR correctly.• Fetal heart rate measurements are labeled in the order in which you plug in the transducers for those measurements. It does not matter which fetal sensor socket you use, as the monitor allocates a channel automatically. For instance, the first transducer you connect is automatically allocated a channel, and the measurement is labeled FHR1, the second is labeled FHR2, and so on.If you need to disconnect the transducers measuring the FHR temporarily, with the intention to continue monitoring after the temporary break (for example, if the mother needs to go to the bathroom), it is important that you reconnect the transducers in the same order as you originally connected them to make sure the measurement labels remain consistent.Upon discharge of the patient all connected transducers are reset from left to right. Example: Only one transducer is still connected to the monitor, it was labeled FHR2 while monitoring the previous discharged patient; it is now reset to FHR1.• The transducer Finder LED lets you identify at a glance which transducer is monitoring which heart rate channel.• The fetal sensor socket to which a transducer is connected is identified by the transducer position indicator in the blue setup menu header:FM20/FM30 FM40/FM50
12 Monitoring Twin FHRs172• The trace recorded for FHR1 is thicker (darker) than that recorded for FHR2. This ensures that the two heart rates are easily distinguishable. The thickness of the recorded trace can be changed in Configuration Mode.• Remember that only one fetal heartbeat can be heard from the loudspeaker at any time.• The audio source symbol shows you which fetus you are listening to. To hear the other fetal heartbeat, select the fetal heart rate sound for this channel (see “Selecting Fetal Heart Sound” on page 158).• Monitor maternal pulse, especially during later stages of labor, to avoid mistaking maternal heart rate for FHR.• Make sure you are recording the best possible signals by referring to the signal quality indicators and repositioning the transducers if necessary.• For the Avalon CL transducer system see “Cableless Monitoring - Important Considerations” on page 156.Monitoring Twins ExternallyTo monitor twin FHRs externally you need two ultrasound transducers. Follow the procedures described in “Monitoring FHR and FMP Using Ultrasound” on page 155. The transducer Finder LED lets you identify at a glance which transducer is monitoring which FHR channel, and lights when you select the FHR numeric field on the screen.Example of the screen showing ultrasound monitoring of twin FHRs:1FHR 12Toco parameter3FHR 2
12 Monitoring Twin FHRs173Monitoring Twins InternallyFM30/50 Monitor one twin using the procedures described in “Monitoring FHR and FMP Using Ultrasound” on page 155. Monitor the second twin using the procedures described in “Monitoring FHR Using DECG” on page 195.Example of a screen showing twin monitoring using a combination of US and DECG (the fetal heart rate monitored via DECG is labeled "DFHR1"/"DFHR2"/"DFHR3" on the screen):Separating FHR TracesTo help you to interpret traces with similar baselines, you can separate the baselines by an offset of 20 bpm by switching trace separation on. For details of the offset, see “Separation Order Type” on page 174.Switching Trace Separation On and OffConnect transducers to the monitor to measure FHR. Depending on the measurement method, you need either two ultrasound transducers or:FM30/50 One ultrasound and one Toco+ transducer, or one CL ECG/IUP transducer (to monitor DECG).1Enter the Main Setup menu by pressing the Main Setup.2Select Fetal Recorder.3Select Trace Separation to toggle between On and Off.4Exit the Main Setup menu.1DFHR 12Toco parameter3FHR 2
12 Monitoring Twin FHRs174Separation Order TypeIn Configuration Mode, you can choose between two different ways, Standard and Classic, for dealing with the trace offsets on the recording (the order in which they are separated) when Trace Separation is On.•Standard: the FHR2 trace is shifted up by 20 bpm (it is recorded 20 bpm higher than it really is). No offset is ever applied to the FHR1 trace - it stays where it is. (In case of a third FHR, this is shifted down by 20 bpm.)•Classic: the FHR1 trace is shifted up by 20 bpm when there is more than one FHR measurement. No offset is ever applied to the FHR2 trace - it stays where it is. (In case of a third FHR, this is shifted down by 20 bpm.)When Trace Separation is OnWhen trace separation is turned on, the recorder prints a dotted line labeled with the two FHRs at the top, and +20 at the bottom.Examples of the two methods (Standard, Classic) for determining the trace separation order are provided here."Standard" Separation OrderTo make differentiating the traces easier, the trace from the ultrasound transducer connected to the FHR2 channel is separated from that of FHR1 by 20 bpm. In other words, the trace for FHR2 is recorded 20 bpm higher than it really is. The trace for FHR1 is never shifted.The recorder prints a dotted line labeled +20 across the FHR scale, to identify the trace for FHR2. The FHR trace is labeled +20 every 5 cm:The label for FHR2 is annotated with a black filled +20:The following trace shows trace separation switched on.
12 Monitoring Twin FHRs175Only the FHR2 trace is offset. The numerical FHR value displayed on the monitor remains unchanged. Subtract 20 from the recorded trace for FHR2 to obtain the true FHR2 value. For example, if the recorded trace shows 160, then the true FHR is 140."Classic" Separation OrderTo make differentiating the traces easier, the trace from the ultrasound transducer connected to the FHR1 channel is separated from that of FHR2 by 20 bpm. In other words, the trace for FHR1 is recorded 20 bpm higher than it really is. The trace for FHR2 is never shifted.The recorder prints a dotted line labeled+20 across the FHR scale, to identify the trace for FHR1. The FHR trace is labeled +20 every 5 cm:The label for FHR1 is annotated with a black filled +20:The following trace shows trace separation switched on.Only the FHR1 trace is offset. The numerical FHR value displayed on the monitor remains unchanged. Subtract 20 from the recorded trace for FHR1 to obtain the true FHR1 value. For example, if the recorded trace shows 160, then the true FHR is 140.
12 Monitoring Twin FHRs176When Trace Separation is OffTo indicate that trace separation is switched off, a dotted line labeled +0 prints across the FHR scale.1Standard trace separation switched off here2Classic trace separation switched off here
12177TroubleshootingCommon problems that may occur when monitoring FHR using ultrasound are listed in “Monitoring FHR and FMP Using Ultrasound” on page 155. See also “Monitoring FHR Using DECG” on page 195 for common problems you might encounter when monitoring FHR directly.The following problem may occur when monitoring twins.For more information, see “Additional Information” on page 163.Problem Possible Cause SolutionThe question mark is printed repeatedly, and appears on the screen and the INOP Coincidence is issued.Both transducers are recording the same FHR, or one fetal transducer is recording the MHR.Reposition an ultrasound transducer. See “Recommended Actions for INOP Coincidence” on page 154.
12 Monitoring Twin FHRs178
13 Monitoring Triple FHRs17913Monitoring Triple FHRsIf your monitor is equipped with the triplets option, it carries the label.You can monitor triple FHRs externally using three ultrasound transducers. With the Avalon CL Transducer system you can now monitor triplets with cableless transducers. The Avalon CTS system does not have this option.Refer to the appropriate preceding chapters for contraindications, and more information about the available measurement methods.FHR detection by the monitor may not always indicate that the fetuses are alive. Confirm fetal life before monitoring, and continue to confirm that the fetuses are the signal source for the recorded fetal heart rates. See “Confirm Fetal Life Before Using the Monitor” on page 10 and “Cross-Channel Verification (CCV)” on page 149.Important Considerations• The procedures and any contraindications that apply for twins monitoring also apply for monitoring triplets. In addition, when monitoring triplets: Be aware that monitoring three FHRs is inherently more difficult than monitoring single or twin FHRs. The nature of the application increases the likelihood that a fetal heart rate is monitored by more than one transducer.• Ensure that you are recording three different fetal heart rates. Pay particular attention to any coincidence of heart rates detected by the monitor's cross-channel verification feature.• Fetal heart rate measurements are labeled in the order in which you plug in the transducers for those measurements. It does not matter which fetal sensor socket you use, as the monitor allocates a channel automatically. For instance, the first transducer you connect is automatically allocated a channel, and the measurement is labeled FHR1, the second is labeled FHR2, and the third FHR3.If you need to disconnect the transducers measuring the FHR temporarily, with the intention to continue monitoring after the temporary break (for example, if the mother needs to go to the bathroom), it is important that you reconnect the transducers in the same order as you originally connected them to make sure the measurement labels remain consistent.Upon discharge of the patient all connected transducers are reset from left to right. Example: Only one transducer is still connected to the monitor, it was labeled FHR2 while monitoring the previous discharged patient; it is now reset to FHR1.• The transducer Finder LED lets you identify at a glance which transducer is monitoring which heart rate channel.
13 Monitoring Triple FHRs180• The fetal sensor socket to which a transducer is connected, is identified by the transducer position indicator in the blue setup menu header:• The trace recorded for the FHR3 is thicker (darker) than that recorded for FHR1, which is thicker than that for FHR2. This ensures that the three heart rates are easily distinguishable. The thickness of the recorded trace can be changed in Configuration Mode.• Remember that only one fetal heartbeat can be heard from the loudspeaker at any time. The audio source symbol shows you which fetus you are listening to. To hear the other fetal heartbeat, select the fetal heart rate sound for this channel (see “Selecting Fetal Heart Sound” on page 158).• Monitor maternal pulse to avoid mistaking maternal heart rate for FHR.• Ensure you are recording the best possible signals by referring to the signal quality indicators and repositioning the transducers if necessary.For the Avalon CL transducer system see “Cableless Monitoring - Important Considerations” on page 156.Monitoring TripletsTo monitor triple FHRs you need three ultrasound transducers. Follow the procedures described in “Monitoring FHR and FMP Using Ultrasound” on page 155 and in “Monitoring Twin FHRs” on page 171. The transducer Finder LED lets you identify at a glance which transducer is monitoring which heart rate channel.Separating FHR TracesTo help you to interpret traces with similar baselines, you can separate the baselines by an offset of 20 bpm by switching trace separation on. For details of the offset, see “Separation Order Type” on page 174."Standard" Separation OrderTo make differentiating the traces easier, the trace for FHR2 is offset by +20 bpm, and the trace for FHR3 is offset by -20 bpm. In other words, the trace for FHR2 is recorded 20 bpm higher than it really is, while the trace for FHR3 is recorded 20 bpm lower than it really is. The trace for FHR1 is never shifted.FM20/FM30 FM40/FM50The recorder prints a dotted line labeled +20 across the FHR scale, to identify the trace for FHR2.
13 Monitoring Triple FHRs181The following trace shows triplets with Trace Separation on, and using Standard separation order.The traces for FHR2 and FHR3 are offset. The numerical FHR values displayed on the monitor remain unchanged. Subtract 20 from the recorded trace for FHR2 to obtain the true FHR2. For example, if the recorded trace shows 160, then the true FHR is 140. Similarly, add 20 to the recorded trace for FHR3 to obtain the true FHR3."Classic" Separation OrderTo make differentiating the traces easier, the trace for FHR1 is offset by +20 bpm, and the trace for FHR3 is offset by -20 bpm. In other words, the trace for FHR1 is recorded 20 bpm higher than it really is, while the trace for FHR3 is recorded 20 bpm lower than it really is. The trace for FHR2 is never shifted.The recorder prints a dotted line labeled -20 across the FHR scale, to identify the trace for FHR3.The FHR trace is labeled every 5 cm.The label for FHR2 is annotated with +20 and the FHR3 label is annotated with -20.The recorder prints a dotted line labeled +20 across the FHR scale, to identify the trace for FHR1.The recorder prints a dotted line labeled -20 across the FHR scale, to identify the trace for FHR3.
13 Monitoring Triple FHRs182The following trace shows triplets with Trace Separation on, and using Classic separation order.The traces for FHR1 and FHR3 are offset. The numerical FHR values displayed on the monitor remain unchanged. Subtract 20 from the recorded trace for FHR1 to obtain the true FHR1. For example, if the recorded trace shows 160, then the true FHR is 140. Similarly, add 20 to the recorded trace for FHR3 to obtain the true FHR3.Switching Trace Separation On and Off1Connect three ultrasound transducers to the monitor to measure FHR.2See “Switching Trace Separation On and Off ” on page 173 for details of how to switch trace separation on or off.When Trace Separation is OnWhen trace separation is turned on, the recorder prints a dotted line labeled with the three FHRs at the top, and ±20 at the bottom. Examples of the two methods (Standard, Classic) for determining the trace separation order are provided here.The FHR trace is labeled every 5 cm.The label for FHR1 is annotated with +20 and the FHR3 label is annotated with -20.
13183When Trace Separation is OffTo indicate that trace separation is switched off, a dotted line labeled +0 prints across the FHR scale.1Standard trace separation switched off here
13 Monitoring Triple FHRs184TroubleshootingCommon problems that may occur when monitoring FHR using ultrasound are listed in “Monitoring FHR and FMP Using Ultrasound” on page 155.The following problem may occur when monitoring triplets.For more information, see “Additional Information” on page 163.2Classic trace separation switched off hereProblem Possible Cause SolutionThe question mark is printed repeatedly, and appears on the screen and the INOP Coincidence is issued.More than one transducer is recording the same FHR, or a fetal transducer records the same heart rate as the MHR.Reposition one or more ultrasound transducer, as appropriate. See “Recommended Actions for INOP Coincidence” on page 154
1418514Fetal Heart Rate AlarmsFetal heart rate (FHR) alarms can give both audible and visual warning of a non-reassuring fetal condition. Your monitor must be configured to alarm mode All to enable the FHR alarms (see “Alarms” on page 109).Changing Alarm SettingsWhen you do any of the following actions for any FHR measurement channel, this applies for all active FHR measurements, both ultrasound and DECG:• Turning FHR alarms on or off.• Changing alarm limits.• Changing alarm delays.• Changing signal loss delay.The monitor retains these settings, even when switched off. The alarm limits are printed on the trace every few pages if alarms are on.Turning Alarms On or Off1Connect either an ultrasound or a DECG transducer to a free socket on the monitor.2Enter the Setup menu for a connected FHR measurement.3Select Alarms to toggle between On and Off.Changing Alarm Limits1Connect either an ultrasound or a DECG transducer to a free socket on the monitor.2Enter the Setup menu for a connected FHR measurement.3To change the high alarm limit, select High Limit and select the alarm limit from the pop-up list.4To change the low alarm limit, select Low Limit and select the alarm limit from the pop-up list.Changing Alarm DelaysYou can change the alarm delays if the Alarm Mode is set to All.1Connect either an ultrasound or a DECG transducer to a free socket on the monitor.2Enter the Setup menu for a connected FHR measurement.
14 Fetal Heart Rate Alarms1863To change the high alarm limit delay time, select High Delay and select the delay time (in seconds) from the pop-up list.4To change the low alarm limit delay time in seconds, select Low Delay and select the delay time (in seconds) from the pop-up list.Changing Signal Loss DelayThe signal loss delay is the configurable delay before a Signal Loss INOP is issued. You can change the delay:1Connect either an ultrasound or a DECG transducer to a free socket on the monitor.2Enter the Setup menu for a connected FHR measurement.3Select SignalLoss Delay and select the signal loss INOP delay time (in seconds) from the pop-up list.
15 Monitoring Uterine Activity Externally18715Monitoring Uterine Activity ExternallyYou can measure uterine activity externally using a Toco transducer. You can also use a Toco+, Toco MP, or a CL Toco+MP transducer for the same purpose, although they also have more (ECG/IUP and Pulse) capabilities.The external Toco transducer measures the frequency, duration and relative strength of contractions, but not their absolute intensity. Amplitude and sensitivity depend on various factors such as the position of the transducer, the belt tension and the size of the patient.What You NeedToco, Toco MP, or Toco+ transducerCL Toco+MP transducers (additionally capable of providing the maternal pulse measurement)CL ECG/IUP transducer
15 Monitoring Uterine Activity Externally188External Toco MonitoringPrepare for Toco monitoring using the list below. The standard procedures in use in your facility determine the sequence of actions.1Fasten the abdominal transducer belt around the patient.2Connect the Toco transducer to a free socket on the monitor. The Toco baseline is automatically reset. The Toco display shows 20. "Toco", indicating external uterine measurement, is printed on the trace at intervals.3Place the transducer on the patient's fundus to ensure the optimum recording of uterine activity.4Reset the Toco baseline as necessary (see “Resetting the Toco Baseline” on page 188), but not during a contraction.The following example trace shows two contractions.Resetting the Toco Baseline1Press the Toco Baseline SmartKey. This resets the Toco baseline to 20 on the display and trace.2If the Toco value is negative for more that five seconds, the Toco baseline is automatically reset to 0 units.Toco SensitivityIf the Toco sensitivity is too high, and the Toco trace exceeds the paper scale, you can reduce the Toco sensitivity to 50%. The default setting is 100%.To change the Toco sensitivity:1Enter the Setup Toco menu.2Select Gain to toggle between 100% and 50%.Abdominal Belt (disposable shown)
15189TroubleshootingTesting Toco TransducersIf any of the following tests fail, repeat the test using another transducer. If the second transducer passes the tests, confirming that the first transducer is defective, contact your service personnel.External Toco MonitoringProblem Possible Causes SolutionsQuality of the trace deteriorates or the Toco baseline variesThe belt is incorrectly fastened and is too slack or too tight, or the belt has lost its elasticity.The belt must be tight enough to ensure good contact between the patient's skin and the entire surface of the transducer without causing discomfort. Ensure you are using the correct belt. Adjust it as necessary.Fetal movement Check if the belt is correctly fastened and adjust it as necessary. Reposition the transducer and reset the Toco baseline if necessary.Maternal respiration superimposed on traceCheck if belt is not too loose.Maternal movement/change of position Following maternal movement, reset Toco baselineToco sensitivity is too high (above 100 units)Toco trace is exceeding the paper scalePhysical transmission of pressure from the uterus to the sensor is much higher than the average value.Check if the belt is too tightly fastened.Select 50% Toco sensitivity.Toco Equip Malf is displayed. See “Patient Alarms and INOPs” on page 121.Toco Unplugged is displayed. See “Patient Alarms and INOPs” on page 121.If you suspect the signal from the transducer. Test the Transducer (see “Testing Toco Transducers” on page 189 below).
15 Monitoring Uterine Activity Externally190If the second transducer also fails the tests, contact your service personnel.You can test all Toco transducers, including the cableless ones, as described above.To test a Toco transducer:1Switch on the monitor and the recorder.2Connect the transducer to the fetal monitor.3Gently apply pressure to the pick-up button.4Check if after a few seconds the values on the display and paper show this change in pressure.
16 Monitoring Uterine Activity Internally19116Monitoring Uterine Activity InternallyFM30/50 You can monitor intrauterine pressure (IUP) using an intrauterine catheter together with a patient module, Toco+, or the CL ECG/IUP transducer, after rupture of the membranes and the cervix is sufficiently dilated.What You NeedIllustration 1 shows the complete connection chain from the IUP catheter to the fetal monitor using the patient module:1Disposable Koala IUP Catheter (M1333A)2Reusable Koala IUP Adapter Cable (9898 031 43931)3Patient Module (M2738A)
16 Monitoring Uterine Activity Internally192Illustration 2 shows the complete connection chain from the IUP catheter to the fetal monitor using the Toco+ transducer:Illustration 3 shows the complete connection chain from the IUP catheter to the fetal monitor using the CL ECG/IUP transducer:1Disposable Koala IUP Catheter (M1333A)2Reusable Koala IUP Adapter Cable (9898 031 43931)3Toco+ transducer (M2735A)1Disposable Koala IUP Catheter (M1333A)2Reusable Koala IUP Adapter Cable (9898 031 43931)3CL ECG/IUP transducer (866077)4Avalon CL base station (866074)
16193Internal (IUP) MonitoringRead the instructions that accompany the intrauterine catheter and the adapter cable before you start monitoring. Zero the monitor when instructed.WARNINGDo not catheterize if placenta previa is diagnosed, or if uterine bleeding from an undetermined source is present.Prepare for IUP monitoring using the list below. The standard procedures in use in your facility determine the sequence of actions.1Perform a complete clinical evaluation.2Catheterize after membrane rupture. Insert the catheter according to its accompanying instructions.3Connect the catheter to the socket on the patient module.4Connect the patient module to a free socket on the monitor. The monitor is automatically zeroed. The IUP display shows 0. "IUP", indicating internal measurement, is printed at intervals on the trace.5Zero the monitor (see “Zeroing the Monitor” on page 193).6If you suspect the catheter is not responding appropriately, flush as directed in the catheter's Instructions for Use. A pressure spike appears on the trace if you flush after connecting the transducer to the monitor.Zeroing the MonitorZero the monitor by selecting the Zero IUP SmartKey, or selecting Zero IUP in the Setup IUP menu. This resets the display and trace to 0. If you do not zero the monitor properly, the pressure trace may exceed the paper scaling.Selecting the IUP UnitYou can select between mmHg (default) and kPa for the IUP unit.1Enter the Setup IUP menu.2Press Unit to toggle between mmHg and kPa.
16 Monitoring Uterine Activity Internally194TroubleshootingInternal (IUP) MonitoringProblem Possible Causes SolutionsNo change in pressure during contraction.Dry environment or possible extra-ovular placement of sensor tip.Refer to catheter Instructions for Use.Only pressure peaks can be seen (baseline not visible).Zero adjustment is incorrect. Zero the system.Trace is a straight line. Transducer is defective. Remove and touch the catheter. If the trace does not show up and down movements, use a new transducer.Catheter blocked. Refer to catheter Instructions for Use.Trace is superimposed with noise.End of catheter is in the uterine wall. Refer to catheter Instructions for Use.IUP Equip Malf INOP is displayed. See “Patient Alarms and INOPs” on page 121.IUP Unplugged INOP is displayed.
17 Monitoring FHR Using DECG19517Monitoring FHR Using DECGFM30/50 This chapter describes how to monitor a single fetal heart rate via direct ECG (DECG), using a spiral fetal scalp electrode in the intrapartum period.Read and adhere to the instructions that accompany the fetal scalp electrode, the DECG adapter cable, and the attachment electrode. Pay attention to all the contraindications, warnings, and for the DECG adapter cable, the cleaning and disinfection procedures.Before starting to monitor, first define the fetal position, and ensure that it is suitable for DECG monitoring.Misidentification of MHR as FHRConfirm fetal life before monitoring, and continue to confirm that the fetus is the signal source for the FHR during monitoring. Here are two examples where the MHR can be misidentified as the FHR when using a fetal scalp electrode:• Electrical impulses from the maternal heart can sometimes be transmitted to the fetal monitor through a recently deceased fetus via the spiral scalp electrode, appearing to be a fetal signal source.• The recorded MHR, and any artifact, can be misinterpreted as a FHR especially when it is over 100 bpm.To reduce the possibility of mistaking the MHR for FHR, monitor both maternal and fetal heart rates (see “Monitoring Maternal Heart / Pulse Rate” on page 223). The monitor's cross-channel verification (CCV) facility can help by automatically detecting when the same heart rate is being recorded by different transducers. See “Confirm Fetal Life Before Using the Monitor” on page 10 and “Cross-Channel Verification (CCV)” on page 149.If the Coincidence INOP is issued at the fetal monitor if you are measuring FHR with DECG:1Confirm that the scalp electrode is placed correctly.2Confirm fetal life by palpation of fetal movement or auscultation of fetal heart sounds using a fetoscope, stethoscope, or Pinard stethoscope. 3If you cannot hear the fetal heart sounds, and you cannot confirm fetal movement by palpation, confirm fetal life using obstetric ultrasonography.4In case of difficulties deriving a stable maternal pulse reading using the Toco MP or CL Toco+MP transducer, use SpO2 instead. In case of similar problems with the pulse measurement from SpO2, use MECG instead. Reasons to switch the method for deriving a maternal pulse or heart rate include: motion artifacts, arrhythmia, and individual differences in pulse signal quality on the abdominal skin (via Toco+MP).
17 Monitoring FHR Using DECG196What You NeedYou can measure fetal DECG using the equipment combinations shown in the following illustrations.WARNINGNever attempt to connect the fetal scalp electrode to anything other than the correct DECG adapter cable.Illustration 1 shows the complete connection chain from the fetal scalp electrode to the fetal monitor using the Toco+ transducer.1Fetal Scalp Electrode, single spiral (9898 031 37631)2Fetal Scalp Electrode, double spiral, Europe only, not for USA (9898 031 37641)3DECG Adapter Cable (9898 031 37651) with Pre-gelled Attachment Electrode (9898 031 39771)4Toco+ transducer (M2735A)
17 Monitoring FHR Using DECG197Illustration 2 shows the equivalent chain using the CL Toco+MP or CL ECG/IUP transducer.1Fetal Scalp Electrode, single spiral (9898 031 37631)2Fetal Scalp Electrode, double spiral, Europe only, not for USA (9898 031 37641)3DECG Adapter Cable (9898 031 37651) with Pre-gelled Attachment Electrode (9898 031 39771)4CL Toco+MP or CL ECG/IUP transducer (866077)5Avalon CL base station (866074)
17 Monitoring FHR Using DECG198Illustration 3 shows the equivalent chain using the patient module.Making ConnectionsWARNINGFollow the instructions supplied with each of the monitoring accessories you are using.Prepare for DECG monitoring using the list below. The standard procedures in use in your facility determine the sequence of actions.1If changing monitoring mode from US to DECG, first disconnect the US transducer.2Depending on the equipment you are using, ensure that the Toco+ transducer, CL Toco+MP, the CL ECG/IUP transducer, or the patient module is connected to the fetal monitor. 3Attach the fetal scalp electrode to the fetus, following the instructions supplied with the fetal scalp electrode.4Attach a pre-gelled attachment electrode to the DECG adapter cable, following the instructions supplied with the DECG adapter cable. 5Fix the attachment electrode to the mother's thigh, following the instructions supplied with the attachment electrode.Depending on the equipment you are using, connect the red connector plug on the DECG adapter cable to the red connector on the Toco+ transducer, CL Toco+MP, the CL ECG/IUP transducer, or the patient module.6Connect the fetal scalp electrode to the DECG adapter cable.1Fetal Scalp Electrode, single spiral, (9898 031 37631)2Fetal Scalp Electrode, double spiral, Europe only, not for USA (9898 031 37641)3DECG Adapter Cable (9898 031 37651) with Pre-gelled Attachment Electrode (9898 031 39771)4Patient Module (M2738A)
17 Monitoring FHR Using DECG199You are now ready to begin monitoring DECG.WARNINGThe fetal/maternal monitor is not a diagnostic ECG device. In particular, the display of fetal/maternal ECG is intended only for evaluating signal quality for fetal/maternal heart rate as derived from the ECG waveform.When in doubt, it can be used to identify sources of compromised signal quality, such as noise or muscle artifacts. It can subsequently be used to verify the result of measures taken to resolve them (e.g. checking ECG cable connections or adapting the fetal ArtifactSuppress configuration).The safety and effectiveness of the displayed fetal/maternal ECG waveform (i.e. P, QRS and T segments) for evaluation of fetal/maternal cardiac status during labor have not been evaluated.Monitoring DECGTo simultaneously measure DECG and MECG, you need the CL ECG/IUP transducer or the patient module for DECG, and a Toco+, CL Toco+MP, or CL ECG/IUP transducer for MECG (see “Monitoring Maternal Heart / Pulse Rate” on page 223). Alternatively, you can monitor the maternal pulse rate via pulse oximetry (see “Pulse Rate from SpO2” on page 230). You can also monitor maternal pulse with the Toco MP or CL Toco+MP transducer. In any case where you would use a Toco+ or Toco MP transducer, you can also monitor with a CL Toco+MP transducer.1Switch on the recorder.2The heart rate monitored via DECG is labeled DFHR1 / DFHR2 / DFHR3 on the screen. If configured, the DECG wave is displayed automatically on the screen, labeled DECG and fetal. If MECG is being monitored, both waves are displayed, with the DECG wave above the MECG wave. The MECG wave is labeled MECG and maternal.
17 Monitoring FHR Using DECG2003Check the artifact suppression setting and change it if necessary (see “Suppressing Artifacts” on page 201).NOTEThe 1mV scale bar for the DECG and MECG wave is not displayed on the screen if you monitor DECG or MECG with an Avalon CTS system. The Avalon CTS system does not provide a scaled ECG. 1Measurement label (FHR1)2Measurement label (Toco)3Measurement label (DFHR2)4Measurement label (FHR3)5Measurement label (SpO2)6Measurement label (HR)71mV scale bar8MECG wave with maternal label9DECG wave with fetal label10 Measurement label (Temp) maternal temperature11 Measurement label NBP
17201WARNINGPeriodically compare the mother's pulse with the signal coming from the monitor's loudspeaker to ensure that you are monitoring fetal heart rate. If the MHR coincides with the FHR, do not misinterpret the MHR as the FHR (see also “Confirm Fetal Life Before Using the Monitor” on page 10 and “Cross-Channel Verification (CCV)” on page 149.Suppressing ArtifactsWhen the monitor's artifact suppression is on, instantaneous heart rate changes of 28 bpm or more, however caused, are not recorded. Fetal arrhythmia will also be suppressed. If you suspect fetal arrhythmia, switch artifact suppression off. When artifact suppression is off, all recorded fetal heartbeats within the specified range are shown. The default setting is On (artifacts are suppressed). To change the setting:1Enter the Setup DFHR1 menu.2Select ArtifactSuppress to toggle between artifact suppression On (artifacts are suppressed) and Off (no artifact suppression, use this setting if you suspect fetal arrhythmia).When artifact suppression is off, Artifact Suppression Off is annotated on the trace recording.Printing the WaveformYou can print the DECG wave onto the trace paper. Refer to “Printing the ECG Waveform” on page 233.
17 Monitoring FHR Using DECG202TroubleshootingTesting DECG ModeSee the monitor's Service Guide.Problem Possible Cause SolutionsDFHR1 Equip MalfDFHR2 Equip MalfDFHR3 Equip MalfMalfunctioning equipment See “Patient Alarms and INOPs” on page 121.DFHR1 Leads OffDFHR2 Leads OffDFHR3 Leads OffNumeric is displayed with a -?-; INOP toneSee also “Patient Alarms and INOPs” on page 121.Erratic traceErratic displayFetal scalp electrode detached at connectorReconnect the fetal scalp electrodeIf the wave is configured to be displayed on the monitor, you can observe if the ECG signal is clear, or if it shows interruptions and noisePoor or no contact between leg attachment electrode and motherCheck all connectionsDisconnect and reconnect the connector several timesNo contact between the DECG adapter cable and the leg attachment electrodeNo contact between the fetal scalp electrode connector and the DECG adapter cableCheck all connectionsDisconnect and reconnect the connector several timesIf problem persists, use a new fetal scalp electrodeNo ECG signalPoor contact between the reference electrode and the motherCheck for fetal demiseUse a new fetal scalp electrode if necessarySignal quality indicator continuously shows a poor signalFetal arrhythmia Use a new fetal scalp electrode if necessaryDFHR1 Signal LossDFHR2 Signal LossDFHR3 Signal LossNo signal See “Patient Alarms and INOPs” on page 121.DFHR1 UnpluggedDFHR2 UnpluggedDFHR3 UnpluggedNo connection See “Patient Alarms and INOPs” on page 121.
18 Monitoring Noninvasive Blood Pressure20318Monitoring Noninvasive Blood PressureThis fetal monitor uses the oscillometric method for the noninvasive blood pressure measurement. In adult mode the blood pressure measurements determined with this device comply with the American National Standard for Electronic or Automated Sphygmomanometers (ANSI/AAMI SP10-1992) in relation to mean error and standard deviation, when compared to intra-arterial or auscultatory measurements (depending on the configuration) in a representative sample population. For the auscultatory reference, the fifth Korotkoff sound was used to determine the diastolic pressure.A physician must determine the clinical significance of the measurement information.Introducing the Oscillometric Noninvasive Blood Pressure MeasurementOscillometric devices measure the amplitude of pressure changes in the occluding cuff as the cuff deflates from above systolic pressure. The amplitude suddenly increases as the pulse breaks through the occlusion in the artery. As the cuff pressure decreases further, the pulsations increase in amplitude, reach a maximum (which approximates to the mean pressure), and then diminish.Studies show that, especially in critical cases (arrhythmia, vasoconstriction, hypertension, shock), oscillometric devices are more accurate and consistent than devices using other noninvasive measuring techniques.WARNINGIntravenous infusion: Do not use the NBP cuff on a limb with an intravenous infusion or arterial catheter in place. This could cause tissue damage around the catheter when the infusion is slowed or blocked during cuff inflation.Skin Damage: Do not measure NBP in cases of sickle-cell disease or any condition where skin damage has occurred or is expected.Unattended measurement: Use clinical judgment to decide whether to perform frequent unattended blood pressure measurements in cases of severe blood clotting disorders, because of the risk of hematoma in the limb fitted with the cuff.Measurement LimitationsMeasurements are impossible with heart rate extremes of less than 40 bpm or greater than 300 bpm, or if the patient is on a heart-lung machine.The measurement may be inaccurate or impossible:• with excessive and continuous patient movement such as during contractions• if a regular arterial pressure pulse is hard to detect• with cardiac arrhythmias
18 Monitoring Noninvasive Blood Pressure204• with rapid blood pressure changes• with severe shock or hypothermia that reduces blood flow to the peripheries• with obesity, where a thick layer of fat surrounding a limb dampens the oscillations coming from the artery• on an edematous extremity.Measurement MethodsThere are three measurement methods:•Manual - measurement on demand. Results are displayed for up to one hour.•Auto - continually repeated measurements (between one and 120 minute adjustable interval). You can make a manual measurement between two measurements in Auto Mode.•Sequence- up to four measurement cycles which will run consecutively, with number of measurements and interval between them configurable for each cycle.Reference MethodThe measurement reference method can be Auscultatory (manual cuff) or Invasive (intra-arterial). For further information, see the Application Note supplied on the monitor documentation DVD.To check the current setting, select Main Setup, Measurements, NBP, and check whether the Reference setting is set to Auscultatory or Invasive. This setting can be changed in Configuration Mode.Preparing to Measure Noninvasive Blood PressureIf possible, avoid taking measurements during contractions because the measurement may be unreliable and may cause additional stress for the patient.1Connect the cuff to the air tubing.2Plug the air tubing into the red NBP connector. Avoid compression or restriction of pressure tubes. Air must pass unrestricted through the tubing.3Make sure that you are using a Philips-approved correct sized cuff and that the bladder inside the cover is not folded or twisted.A wrong cuff size, and a folded or twisted bladder, can cause inaccurate measurements. The width of the cuff should be in the range from 37% to 47% of the limb circumference. The inflatable part of the cuff should be long enough to encircle at least 80% of the limb.4Apply the cuff to a limb at the same level as the heart. If it is not, you must use the measurement correction formula to correct the measurement.The marking on the cuff must match the artery location. Do not wrap the cuff too tightly around the limb. It may cause discoloration, and ischemia of the extremities. Inspect the application site regularly to ensure skin quality and inspect the extremity of the cuffed limb for normal color, warmth and sensitivity. If the skin quality changes, or if the extremity circulation is being affected, move the cuff to another site or stop the blood pressure measurements immediately. Check more frequently when making automatic or stat measurements.
18 Monitoring Noninvasive Blood Pressure205Correcting the Measurement if Limb is not at Heart LevelTo correct the measurement if the limb is not at heart level, to the displayed valueUnderstanding the NumericsDepending on the numeric size, not all elements may be visible. Your monitor may be configured to display only the systolic and diastolic values. If configured to do so, the pulse from NBP will display with the NBP numeric.Aging NumericsThe measured NBP value, together with the corresponding pulse rate if this is switched on, will be displayed for one hour. After that the values are regarded as invalid and are no longer displayed. During this time, measurement values may be grayed out or disappear from the screen after a set time, if configured to do so. This avoids older numerics being misinterpreted as current data. The time can be set in Configuration Mode. In Auto Mode the measurement values may disappear more quickly (to be replaced by new measurement values), if the repeat time is set to less than one hour.NBP and SpO2 numerics from intermittent measurements can be configured to be grayed out or to disappear from the screen after a set time. This avoids older numerics being misinterpreted as current data. The time can be set individually for SpO2 and NBP in Configuration Mode.Alarm SourcesIf you have parallel alarm sources, the sources are displayed instead of the alarm limits.Add 0.75 mmHg (0.10 kPa) for each centimeter higher orDeduct 0.75 mmHg (0.10 kPa) for each centimeter lower orAdd 1.9 mmHg (0.25 kPa) for each inch higher. Deduct 1.9 mmHg (0.25 kPa) for each inch lower.1Alarm source2Measurement Mode3Timestamp/Timer4Mean pressure5Diastolic6Systolic7Alarm limits
18 Monitoring Noninvasive Blood Pressure206NBP Measurement TimestampDepending on your configuration, the time shown beside the NBP numeric can be:– the time of the most recent NBP measurement, also known as the "timestamp", or– the time until the next measurement in an automatic series, displayed with a graphic representation of the remaining time, as shown here.• The NBP timestamp will normally show the completion time of the NBP measurement.NBP Measurement Start TimeIn Auto or Sequence mode the monitor is configured to synchronize the measurements in a measurement series to an "easy-to-document" time. For example, if you start the first measurement at 08:23, and the Repeat Time is set to 10 min, the monitor automatically performs the next measurement at 8:30, then 8:40 and so on, unless it has been configured to NotSynchron..During MeasurementsThe cuff pressure is displayed instead of the units and the repeat time. An early systolic value gives you a preliminary indication of the systolic blood pressure during measurement.Starting and Stopping MeasurementsUse the Setup menu or the SmartKeys to start and stop measurements.Action to be performed Setup menu SmartKeysStart/Stop manual measurementStart Auto seriesStop current automatic measurementStart/StopStart/ StopStart manual measurementStart Auto series-StartStop manual measurementStop current automatic measurement-StopStop automatic, or manual measurement AND series Stop All NBPStop All
18 Monitoring Noninvasive Blood Pressure207Enabling Automatic Mode and Setting Repetition Time1In the Setup NBP menu, select Mode.2Toggle between Auto and Manual, if necessary, to pick the measurement method.3If making an automatic measurement, select Repeat Time or press the Repeat Time SmartKey and set the time interval between two measurements.NOTEBe aware that a combination of a recorder speed of less than 3 cm/min and a repetition time of less than five minutes can result in not all noninvasive blood pressure measurements being recorded on the fetal trace. For example, if the recorder speed is set to 1 cm/min and the repetition time is set to two minutes, due to the low speed setting, the recorder will only be able to record every other noninvasive blood pressure measurement. This affects only the local fetal trace recording, and all measurements are displayed as normal on the monitor's screen.Enabling Sequence Mode and Setting Up The Sequence1In the Setup NBP menu, select Mode and select Sequence from the pop-up menu.2Select Setup Sequence to open the Setup Sequence window.Up to four measurement cycles can be setup which will run consecutively. For each cycle you can set the number of measurements and the interval between them. If you want to run less than four cycles in a sequence, you can set the number of measurements for one or more cycles to Off.3Select each sequence in turn, and select the number of measurements and the time interval between the measurements.4To have measurements continue after the sequence, set the number of measurements for your last cycle to Continuous and this cycle will run indefinitely.CAUTIONBe aware that, if none of the cycles are set to Continuous, NBP monitoring will end after the last measurement of the cycle.When the NBP measurement mode is set to Sequence, the repetition time for Auto Mode cannot be changed.
18 Monitoring Noninvasive Blood Pressure208Choosing the Alarm SourceYou can monitor for alarm conditions in systolic, diastolic, and mean pressure, either singly or in parallel. Only one alarm is given, with the priority of mean, systolic, diastolic.If mean is not selected as alarm source (Sys., Dia., or Sys & Dia selected), but the fetal monitor can only derive a mean value, mean alarms will nevertheless be announced using the most recent mean alarm limits. Check that the mean alarm limits are appropriate for the patient, even when not using mean as the alarm source. When no value can be derived an NBP Measure Failed INOP will be displayed.Assisting Venous PunctureYou can use the cuff to cause sub-diastolic pressure. The cuff deflates automatically after a set time if you do not deflate it.1In the Setup NBP menu select VeniPuncture.2Puncture vein and draw blood sample.3Reselect VeniPuncture to deflate the cuff.During measurement, the display shows the inflation pressure of the cuff and the remaining time in venous puncture mode.Calibrating NBPNBP is not user-calibrated. NBP pressure transducers must be verified at least once every two years by a qualified service professional, and calibrated, if necessary. See the Service Guide for details.Menu option Pressure value monitoredSys. systolicDia. diastolicMean meanSys & Dia systolic and diastolic in parallelDia & Mean diastolic and mean in parallelSys & Mean systolic and mean in parallelSys&Dia&Mean all three pressures in parallel1Cuff pressure2Venous puncture measurement mode3Time left in venous puncture mode
18209TroubleshootingProblem Possible Causes SolutionsCuff will not inflate Monitor is in Service or Configuration ModeTechnical defect Call serviceCuff tubing not connected Connect cuff tubingHigh or low values measured (against clinical expectations)Contraction occurring Wait until contraction has finishedPatient talking before or during measurementAllow patient to rest quietly, then try again after three to five minutesIncorrect cuff size or cuff not at heart levelCheck cuff size, level, and positionNoninvasive blood pressure reference method set incorrectlyCheck the reference method configured (auscultation or intra-arterial) and correct if necessary in Configuration ModeDisplays zeros for systolic and diastolic values. Measurement automatically repeatsSevere vasoconstriction at cuff site Move cuff to another limb, check for shock, or verify blood pressure using another methodErratic blood pressure fluctuations due to arrhythmias or rapid-acting drugs or contractionsTry again, if unsuccessful, verify blood pressure using another methodWait until contraction has finished.Excessive patient movement or convulsionsRestrain movement or verify blood pressure using another methodNBP Cuff Overpress INOP is displayed See “Patient Alarms and INOPs” on page 121.NBP Equip Malf INOP is displayedNBP Interrupted INOP is displayedNBP Measure Failed
18 Monitoring Noninvasive Blood Pressure210
19 Monitoring Maternal Temperature21119Monitoring Maternal TemperatureMeasuring Tympanic TemperatureThe tympanic thermometer measures the patient's temperature in the ear using infrared technology.The result of this measurement can be automatically adjusted to correspond to a different body reference site. The result is displayed on the screen of the thermometer and transmitted to the monitor.The thermometer is used with single-use probe covers for infection control during measurement.WARNINGDo not use in the presence of flammable anesthetics, such as a flammable anesthetic mixture with air, oxygen or nitrous oxide.Place the thermometer into its base station, when it is not in use. The base station allows flexible mounting of the thermometer at the point of care. The base station is connected to the monitor's MIB/RS232 interface (optional) via a cable. It has storage space for up to 32 probe covers.1Base station2Thermometer
19 Monitoring Maternal Temperature212Thermometer Display and ControlsThe tympanic thermometer has a liquid crystal display. The display shows the patient's temperature in numerics and guides you with symbols through the measurement process.1Eject key2Change unit key: °Celsius / °Fahrenheit3Start measurement key4Pulse timer keyFunctional Keys Description of UsePress the eject key to eject the probe cover. The eject key symbol is shown on the display when a measurement has been taken and transmitted.Press the change unit key after a measurement to switch between °C and °F.Press the start measurement key when you are ready to take a patient's temperature.The pulse timer key can be used to time vital signs you take manually.Press and hold the pulse timer key to enter timer mode. Press the pulse timer key again to start the timer.The thermometer will issue a one beep at 15 seconds, two beeps at 30 seconds, three beeps at 45 seconds, and four beeps at 60 seconds.
19 Monitoring Maternal Temperature213Status ScreensThe thermometer performs an internal test at every start-up to verify that the system components are functioning properly. It measures the ambient temperature. During start-up and measurement, the thermometer screens communicate the current status.Making a Temperature MeasurementWARNINGInaccurate measurement results can be caused by:• incorrect application of the thermometer.• anatomical variations in the ear.• build up of earwax in the ear.• excessive patient movement during the measurement.• absent, defective or soiled probe covers.• probe covers other than the specified probe covers.1Ensure that the base station is connected via the appropriate cable to the connector on the monitor.2Remove the thermometer from the base station.The thermometer is latched to the base station to avoid an accidental fall when the base station is moved. To pick up the thermometer from the base station move it slightly up and then lift it from the base station to release the latch.3Press the eject key on the thermometer to discard any probe that may have been left on the thermometer from a previous use.Images Description Ambient Temperature above specified rangeAmbient Temperature below specified rangeSystem errorsSystem error 12 - there is a problem with the settings. Contact your service personnel to have them check the settings and reset them, if necessary.If the display shows any other system error, then reset the thermometer by picking up a probe cover. If the system error does not clear, contact your service personnel.
19 Monitoring Maternal Temperature2144Pick up a new probe from the probe container on the base station. 5Inspect the probe cover to make sure it is fully seated (no space between cover and tip base) and there are no holes, tears, or wrinkles in the plastic film.6Place the thermometer with the probe in the ear canal, sealing the opening with the probe tip. For consistent results, ensure that the probe shaft is aligned with the ear canal.7Press and release the start-up key gently.8Wait until you hear the three beeps.9Remove the probe from the ear.The temperature values are displayed both on the thermometer itself and on the connected monitor.10 Check that the correct temperature label for the measurement site is displayed: iTrect, iToral, iTcore, or iTtymp11 Press the eject key to eject the probe cover into a suitable waste receptacle.12 Return the thermometer to the base station.The thermometer switches to stand-by mode after 30 seconds when not used.Possible INOPsImages DescriptionPatient temperature above measurement range.Patient temperature below measurement range.
19215WARNING• Never apply the probe to the patient when the probe is not connected to the unit.• Always use a single-use probe cover to limit patient cross-contamination.• Measurement errors or inaccurate readings may result when probe covers other than the specified probe covers are used (see “Tympanic Temperature Accessories” on page 267)• Insert the probe slowly and carefully to avoid damage to the ear canal and the tympanic membrane.• Inspect the probe for damage, holes, tears, or sharp edges to avoid injuring the skin.• Always ensure that the used probe cover is removed before attaching a new probe cover.CAUTION• Do not immerse the probe in fluids, or drop fluids on the probe.• Do not use a probe cover that has been dropped or is damaged.• Do not autoclave. To prevent damage to the unit, probe and accessories, refer to the cleaning procedures in the “Cleaning and Disinfecting” on page 246 chapter.Body Reference Sites and Monitor LabelsThe tympanic thermometer measures the patient's temperature in the ear. The thermometer can be configured to adjust the result of the measurement to correspond to a different body reference site. The measurement label displayed on the monitor corresponds to the body reference site that is configured. The following body reference sites are available:The body reference site can be selected in the Biomed mode of the tympanic thermometer. See the Service Guide for more information.The measured maternal temperature is only transmitted to a connected OB TraceVue/IntelliSpace Perinatal, when the tympanic thermometer is configured to the iTtymp body reference site, and the iTtymp label is displayed on the fetal monitor screen and printed out on the trace paper. Body Reference Site Label on MonitorEar temperature (no adjustment) iTtympOral temperature iToralCore temperature iTcoreRectal temperature iTrect
19 Monitoring Maternal Temperature216Entering Temperature ManuallyA temperature measurement can be entered manually.1Press the SmartKey Enter Temp.2A numeric pad opens.3Enter the temperature values.4Press the Enter key.The aging time (time the entered value is valid) can be configured in the Configuration Mode.
20 Monitoring SpO221720Monitoring SpO2FM30/40/50 The pulse oximetry measurement (SpO2) is intended for use with maternal patients.Philips pulse oximetry uses a motion-tolerant signal processing algorithm, based on Fourier Artifact Suppression Technology (FAST). It provides two measurements:• Oxygen saturation of arterial blood (SpO2) - percentage of oxygenated hemoglobin in relation to the sum of oxyhemoglobin and deoxyhemoglobin (functional arterial oxygen saturation).• Pulse rate - detected arterial pulsations per minute. This is derived from the SpO2 value, and is one of four sources of the maternal heart/pulse rate used for cross-channel verification (see “Monitoring Maternal Heart / Pulse Rate” on page 223 and “Cross-Channel Verification (CCV)” on page 149).Selecting an SpO2 SensorSee “Accessories and Supplies” on page 257 for a list of sensors, and the patient population and application sites for which they are appropriate.Familiarize yourself with the Instructions for Use supplied with your sensor before using it.CAUTIONDo not use OxiCliq disposable sensors in a high humidity environment, or in the presence of fluids, which may contaminate sensor and electrical connections causing unreliable or intermittent measurements. Do not use disposable sensors when there is a known allergic reaction to the adhesive.Applying the Sensor1Follow the SpO2 sensor's Instructions for Use, adhering to all warnings and cautions.2Remove colored nail polish from the application site.3Apply the sensor to the patient. The application site should match the sensor size so that the sensor can neither fall off, nor apply excessive pressure.4Check that the light emitter and the photodetector are directly opposite each other. All light from the emitter must pass through the patient's tissue.
20 Monitoring SpO2218WARNINGProper Sensor Fit: If a sensor is too loose, it might compromise the optical alignment or fall off. If it is too tight, for example because the application site is too large or becomes too large due to edema, excessive pressure may be applied. This can result in venous congestion distal from the application site, leading to interstitial edema, hypoxemia and tissue malnutrition. Skin irritations or lacerations may occur as a result of the sensor being attached to one location for too long. To avoid skin irritations and lacerations, periodically inspect the sensor application site and change the application site regularly.Venous Pulsation: Do not apply sensor too tightly as this results in venous pulsation which may severely obstruct circulation and lead to inaccurate measurements.Ambient Temperature: At elevated ambient temperatures be careful with measurement sites that are not well perfused, because this can cause severe burns after prolonged application. All listed sensors operate without risk of exceeding 41°C on the skin if the initial skin temperature does not exceed 35°C.Extremities to Avoid: Avoid placing the sensor on extremities with an arterial catheter, an NBP cuff or an intravascular venous infusion line.Connecting SpO2 CablesConnect the sensor cable to the color-coded socket on the monitor. If you are using a disposable sensor, plug the sensor into the adapter cable and connect this to the monitor. Connect reusable sensors directly to the monitor.CAUTIONExtension cables: Do not use more than one extension cable (M1941A). Do not use an extension cable with Philips reusable sensors or adapter cables with part numbers ending in -L (indicates "long" cable version).Electrical Interference: Position the sensor cable and connector away from power cables, to avoid electrical interference.Measuring SpO2During measurement, ensure that the application site:– has a pulsatile flow, ideally with a signal quality indicator of at least medium.– has not changed in its thickness (for example, due to edema), causing an improper fit of the sensor.
20 Monitoring SpO2219WARNING• For fully conscious maternal patients, who have a normal function of perfusion and sensory perception at the measurement site:To ensure skin quality and correct optical alignment of the sensor, inspect the application site when the measurement results are suspicious or when the patient complains about pressure at the application site, but at least every 24 hours. Correct the sensor alignment if necessary. Move the sensor to another site, if the skin quality changes.• For all other patients:Inspect the application site every two to three hours to ensure skin quality and correct optical alignment. Correct the sensor alignment if necessary. If the skin quality changes, move the sensor to another site. Change the application site at least every four hours.• Injected dyes such as methylene blue, or intravascular dyshemoglobins such as methemoglobin and carboxyhemoglobin may lead to inaccurate measurements.• Inaccurate measurements may result when the application site for the sensor is deeply pigmented or deeply colored, for example, with nail polish, artificial nails, dye or pigmented cream.• Interference can be caused by:– High levels of ambient light (including IR warmers) or strobe lights or flashing lights (such as fire alarm lamps). (Hint: cover application site with opaque material).– Another SpO2 sensor in close proximity (e.g. when more than one SpO2 measurement is performed on the same patient). Always cover both sensors with opaque material to reduce cross-interference.– Electromagnetic interference, especially at perfusion indicator values below 1.0 or signal quality indicator below medium.– Excessive patient movement and vibration.SpO2 Signal Quality Indicator (Fast SpO2 only)The SpO2 numeric is displayed together with a signal quality indicator (if configured and enough space is available) which gives an indication of the reliability of the displayed values.The level to which the triangle is filled shows the quality of the signal; the indicator below shows a medium signal quality, the signal quality is at a maximum when the triangle is completely filled.
20 Monitoring SpO2220Assessing a Suspicious SpO2 ReadingTraditionally, pulse rate from SpO2 was compared with heart rate from ECG to confirm the validity of the SpO2 reading. With newer algorithms, such as FAST-SpO2, this is no longer a valid criteria because the correct calculation of SpO2 is not directly linked to the correct detection of each pulse.When pulse rate is very low, or strong arrhythmia is present, the SpO2 pulse rate may differ from the heart rate calculated from ECG but this does not indicate an inaccurate SpO2 value.WARNINGWith pulse oximetry, sensor movement, ambient light (especially strobe lights or flashing lights) or electromagnetic interference can give unexpected intermittent readings when the sensor is not attached. Especially bandage-type sensor designs are sensitive to minimal sensor movement that might occur when the sensor is dangling.Understanding SpO2 AlarmsThis refers to SpO2 specific alarms. See the “Alarms” on page 109 chapter for general alarm information. SpO2 offers high and low limit alarms, and a high priority desat alarm. You cannot set the low alarm limit below the desat alarm limit.CAUTIONIf you measure SpO2 on a limb that has an inflated noninvasive blood pressure cuff, a non-pulsatile SpO2 INOP can occur. If the fetal monitor is configured to suppress this alarm there may be a delay of up to 60 seconds in indicating a critical status, such as sudden pulse loss or hypoxia.Alarm DelaysThere is a delay between a physiological event at the measurement site and the corresponding alarm at the monitor. This delay has two components:• The general system delay time is the time between the occurrence of the physiological event and when this event is represented by the displayed numerical values. This delay depends on the algorithmic processing and the averaging time.• The time between the displayed numerical values crossing an alarm limit and the alarm indication on the monitor. This delay is the combination of the configured alarm delay time plus the general system alarm signal delay time.Adjusting the SpO2 Alarm LimitsIn the Setup SpO₂ menu:•Select High Limit then choose the upper alarm limit.•Select Low Limit then choose the lower alarm limit.
20221Adjusting the Desat Limit AlarmThe Desat alarm is a high priority (red) alarm notifying you of potentially life threatening drops in oxygen saturation.1In the Setup SpO₂ menu, select Desat Limit.2Adjust the limit.Adjusting the Pulse Alarm LimitsSee “Adjusting the Heart Rate / Pulse Alarm Limits” on page 230.Setting Up Tone ModulationIf tone modulation is on, the QRS tone pitch lowers when the SpO2 level drops. Remember, the QRS tone is derived from either heart rate (from MECG) or pulse (from built-in SpO2) depending on which is currently displayed (see “Priority for Maternal Heart / Pulse Rate” on page 223).NOTEPulse from CL SpO2 and Toco MP does not provide a QRS tone.Setting the QRS VolumeIn the Setup SpO₂ menu, select QRS Volume and set the appropriate QRS tone volume.
20 Monitoring SpO2222
21 Monitoring Maternal Heart / Pulse Rate22321Monitoring Maternal Heart / Pulse RateYou can monitor the maternal heart/pulse rate using one of four sources:• Maternal pulse from Toco MP or CL Toco+MP transducer (pulse rate)•SpO2 (pulse rate)• Maternal heart rate (MHR) via MECG electrodes• NBP (pulse rate)Maternal heart / pulse rates derived from Toco MP or CL Toco+MP, SpO2 and MECG are continuous measurements, and are compared against the FHR for cross-channel verification. Average pulse rate derived from noninvasive blood pressure is an intermittent measurement, and is therefore not used for cross-channel verification.Priority for Maternal Heart / Pulse RateOnly one Maternal Heart Rate / Pulse Rate numeric will be displayed and recorded at a time (see priority table). If higher-priority measurements are connected but temporarily not providing valid numerics, lower-priority numerics may be displayed and recorded instead. Misidentification of MHR for FHRTo reduce the possibility of mistaking the MHR for FHR, it is recommended that you monitor both maternal and fetal heart rates (see “Confirm Fetal Life Before Using the Monitor” on page 10 and “Cross-Channel Verification (CCV)” on page 149).Priority Maternal Heart / Pulse Rate Source Alarming Used for CCV Provides QRS Tone1 HR from MECG measurement Yes Yes Yes2 Pulse from SpO2 measurement Yes Yes Yes3 Pulse from CL SpO2 Pod measurement Yes Yes No4 Pulse from Toco MP measurement cableless or cabled No Yes No5 Pulse from CL NBP Pod measurement No No No6 Pulse from NBP measurement No No No
21 Monitoring Maternal Heart / Pulse Rate224MHR from MECG ElectrodesYou can measure MHR using the equipment combinations shown in the following illustrations.Illustration 1 shows the complete connection chain from the foam electrodes applied to the patient to the fetal monitor using the patient module.Illustration 2 shows the equivalent chain using the Toco+ transducer.1Patient Module (M2738A)2MECG Adapter Cable (M1363A)3Pre-gelled Foam Electrodes (40493A/B/C/D/E)1Toco+ Transducer (M2735A)2MECG Adapter Cable (M1363A)3Pre-gelled Foam Electrodes (40493A/B/C/D/E)
21 Monitoring Maternal Heart / Pulse Rate225Illustration 3 shows the equivalent chain using a CL Toco+MP transducer or a CL ECG/IUP transducer.To simultaneously measure DECG and MECG, you can use a Toco+, a CL Toco+MP, or a CL ECG/IUP transducer for MECG. For measuring DECG you need a CL ECG/IUP transducer or a patient module (see also “Monitoring FHR Using DECG” on page 195).1Avalon CL base station (866074)2CL Toco+MP or CL ECG/IUP transducer (866075 or 866077)3MECG Adapter Cable (M1363A)4Pre-gelled Foam Electrodes (40493A/B/C/D/E)
21 Monitoring Maternal Heart / Pulse Rate226Applying ElectrodesTo derive the MHR (when you do not want to view the MECG waveform), you can place the electrodes just below the outer end of the clavicle near each shoulder.Making ConnectionsWARNINGFollow the instructions supplied with each of the monitoring accessories you are using.Prepare for monitoring MHR using the list below. The standard procedures in use in your facility determine the sequence of actions.1Depending on the equipment you are using, ensure that either the Patient Module or the Toco+ transducer is connected to the fetal monitor. If you are using cableless monitoring use the CL ECG/IUP or the CL Toco+MP transducer. 2Connect a pre-gelled foam electrode to each of the two leads on the MECG adapter cable.3Apply the foam electrodes to the patient, following the instructions supplied with the foam electrodes.4Depending on the equipment you are using, connect the pink connector plug on the MECG adapter cable to the pink connector on either the Patient Module or the Toco+ transducer. If you are using cableless monitoring connect the MECG Adapter cable to the connectors of the CL ECG/IUP or the CL Toco+MP transducer. You are now ready to monitor MHR.Monitoring MHR1Switch on the recorder.2The maternal heart rate is labeled HR on the screen.1MECG Electrodes
21 Monitoring Maternal Heart / Pulse Rate227Monitoring MECG WaveWARNINGThe fetal/maternal monitor is not a diagnostic ECG device. In particular, the display of fetal/maternal ECG is intended only for evaluating signal quality for fetal/maternal heart rate as derived from the ECG waveform.When in doubt, it can be used to identify sources of compromised signal quality, such as noise or muscle artifacts. It can subsequently be used to verify the result of measures taken to resolve them (e.g., checking ECG cable connections or adapting the fetal ArtifactSuppress configuration).The safety and effectiveness of the displayed fetal/maternal ECG waveform (i.e., P, QRS and T segments) for evaluation of fetal/maternal cardiac status during labor have not been evaluated.FM30/50 When measuring MECG with the Avalon FM30 or FM50, the MECG waveform, along with the heart rate numeric, is displayed on the screen when using a Toco+, CL Toco+MP transducer, a patient module, or a CL ECG/IUP transducer.WARNINGThe fetal/maternal monitor is NOT intended for use during defibrillation, electro-surgery, or MRI. Remove all transducers, sensors, and accessories before performing electro-surgery, defibrillation, or MRI, otherwise harm to the patient or the user can result.Applying ElectrodesTo obtain a satisfactory maternal ECG waveform you must use the RA to LL (lead II) position of the standard 5-lead ECG.1Place the RA electrode (A) directly below the clavicle and near the right shoulder.2Place the LL electrode (B) on the left lower abdomen.
21 Monitoring Maternal Heart / Pulse Rate228Viewing the Waveform on the ScreenNOTEThe 1mV scale bar for the DECG and MECG wave is not displayed on the screen if you monitor DECG or MECG with an Avalon CTS system. The Avalon CTS system does not provide a scaled ECG. For the FM30/50, the MECG wave is displayed automatically on the screen, labeled MECG. If DECG is also being monitored (FM30/50), and the DECG Wave is configured to On, both waves are displayed, with the DECG Wave above the MECG wave. The DECG Wave is labeled DECG.1Measurement label (FHR1)2Measurement label (Toco)3Measurement label (DFHR3)4Measurement label (FHR1)5Measurement label (SpO2)6Measurement label (HR)71mV scale bar8MECG wave with maternal label9DECG wave with fetal label10 Measurement label (Temp) maternal temperature11 Measurement label NBP
21229TroubleshootingPrinting the WaveformYou can print the MECG wave onto the trace paper. Refer to “Printing the ECG Waveform” on page 233.Pulse Rate from Toco MPThe maternal pulse is taken from the Toco MP or CL Toco+MP transducer when SpO2 or MECG measurements are not used or have signal loss. When the pulse rate is very low, or strong arrhythmia is present, the pulse rate measured by the Toco MP or CL Toco+MP transducer may differ from the heart rate calculated from MECG. If the mother is moving about, or began pressing during the second stage of labor, this can cause longer gaps in the recording of the maternal pulse signal. In this case use the SpO2 or MECG measurement to derive the maternal heart rate.Problem Possible Causes SolutionsMECG Leads Off displayed.Numeric is displayed with a -?- for 10 seconds;INOP toneSee also “Patient Alarms and INOPs” on page 121One or more MECG leads is not attached.Make sure that all required leads are attachedIf the wave is configured to be displayed on the monitor, you can observe if the ECG signal is clear, or if it shows interruptions and noiseBad electrical contact Check positioning of the electrode, ensuring that none are displacedCheck electrodes and replace if necessaryElectrodes defectiveprints repeatedlyThe ultrasound transducer is measuring maternal pulse.Reposition the ultrasound transducer. See “Recommended Actions for INOP Coincidence” on page 154MECG Equip Malf displayedEquipment malfunctions See “Patient Alarms and INOPs” on page 121.MECG Unplugged Equipment not connected
21 Monitoring Maternal Heart / Pulse Rate230WARNING• No alarm is possible when Toco MP or CL Toco+MP transducer is the source of the pulse rate.• No QRS tone is audible when Toco MP or CL Toco+MP transducer is the source of the pulse rate.• The Toco MP or CL Toco+MP transducer signal is significantly less reliable if the patient is up and moving about, or is pushing during the second stage of labor.NOTEIn rare cases it is possible to pick up a fetal signal source. When a Toco MP or CL Toco+MP transducer is connected to the monitor but not applied to the patient, the measurement may generate unexpected intermittent pulse readings.Pulse Rate from SpO2If you are not monitoring MHR via MECG electrodes, but you are monitoring SpO2, the maternal pulse rate is derived from the SpO2 measurement. The pulse numeric is labeled Pulse on the screen.WARNINGNo QRS tone is audible when the CL SpO2 Pod is the source of the pulse rate.Adjusting the Heart Rate / Pulse Alarm LimitsTo adjust the pulse alarm limits for SpO2:1In the Setup SpO₂ menu, select Pulse (SpO₂). This opens the Setup Pulse (SpO₂) menu.2Ensure Pulse (SpO₂) is On. Select Pulse (SpO₂) to toggle between On and Off.3Set the pulse alarm limit:– Select High Limit then choose the upper alarm limit for tachycardia from the pop-up list.– Select Low Limit then choose the lower alarm limit for bradycardia from the pop-up list.To adjust the pulse alarm limits for MECG:1In the Setup MECG menu, select MECG/Pulse Alarms. This opens the Setup Pulse (MECG) menu.2Ensure Pulse MECG is On. Select Pulse MECG to toggle between On and Off.3Set the pulse alarm limit.– Select High Limit then choose the upper alarm limit for tachycardia from the pop-up list.– Select Low Limit then choose the lower alarm limit for bradycardia from the pop-up list.
21 Monitoring Maternal Heart / Pulse Rate231Average Pulse Rate from Noninvasive Blood PressureWARNINGNo alarm is possible when noninvasive blood pressure is the source of the pulse rate.When you are measuring noninvasive blood pressure, the monitor can also calculate the average pulse rate. This occurs in either manual or automatic mode, when neither MECG, SpO2 nor pulse from Toco MP or CL Toco+MP transducer are measured. The value is displayed on the screen, and printed on the trace. It is not the actual pulse value, but an average pulse rate, taken during the most recent noninvasive blood pressure measurement. The value is updated after each successive measurement. If you need a continuous measurement, you should monitor using MECG, SpO2 or pulse from Toco MP or CL Toco+MP transducer.Testing MECG ModeSee the monitor's Service Guide.
21 Monitoring Maternal Heart / Pulse Rate232
22 Printing the ECG Waveform23322Printing the ECG WaveformFM30/50 You can print the ECG wave onto the trace paper. If you are monitoring both DECG and MECG, both waves will be printed. The start of the wave recording is annotated above the wave with MECG for Maternal ECG, with DECG for Direct fetal ECG, and with 25 mm/sec below the wave.WARNINGThe fetal/maternal monitor is not a diagnostic ECG device. In particular, the display of fetal/maternal ECG is intended only for evaluating signal quality for fetal/maternal heart rate as derived from the ECG waveform.When in doubt, it can be used to identify sources of compromised signal quality, such as noise or muscle artifacts. It can subsequently be used to verify the result of measures taken to resolve them (e.g., checking ECG cable connections or adapting the fetal ArtifactSuppress configuration).The safety and effectiveness of the displayed fetal/maternal ECG waveform (i.e., P, QRS and T segments) for evaluation of fetal/maternal cardiac status during labor have not been evaluated.The ECG waveform is printed along the bottom of the heart rate grid, and the three different possibilities look like this:DECG waveform on its own1DECG2Paper speed
22 Printing the ECG Waveform234MECG waveform on its ownDECG and MECG waveformsWhen the recorder is on, there are two choices for printing the ECG wave:•Separate: This recording mode gives you a six-second ECG strip on the fetal trace paper in fast printout mode. The real-time fetal trace recording is temporarily interrupted while the ECG strip 1MECG2Paper speed1DECG2Paper speed
22235prints. A new trace header is printed out to mark where the MECG print-out starts and another FHR header mark signals when the fetal trace resumes. The following trace shows the MECG waveform:•Overlap: This recording mode gives you a delayed six-second snapshot of the maternal and/or direct fetal ECG for documentation on the fetal strip, but without interrupting the fetal trace. It takes 5 minutes to print this six-second snapshot at a recorder speed of 3 cm/min. It is documented as if it was recorded at 25 mm/s.1FHR1 trace interrupted2MECG header3Paper speed4FHR1 trace resume
22 Printing the ECG Waveform236The following trace shows both the DECG and MECG waveforms:To make your choice:1Enter the Main Setup menu.2Select Fetal Recorder to enter the Fetal Recorder menu.3Select ECG Wave to toggle between Separate and Overlap.To print the ECG wave(s):EitherSelect the Record ECG Wave SmartKey.Or1Enter the Main Setup menu by selecting the SmartKey.2Select Fetal Recorder to enter the Fetal Recorder menu.3Select Record ECG Wave.1FHR1 and FHR22DECG header3MECG header4Paper speed
22237Or1Select the ECG Wave.2Select Record ECG Wave in the ECG wave menu.
22 Printing the ECG Waveform238
23 Paper Save Mode for Maternal Measurements23923Paper Save Mode for Maternal MeasurementsYour monitor's recorder features a Paper Save Mode, where maternal vital signs are recorded using less paper than during a normal trace recording.When Paper Save Mode is enabled, and if the recorder is stopped, it will start automatically to print data from maternal measurements as they occur, and then stop again to save paper. You enable Paper Save Mode in Configuration Mode (default is off).• A header is printed first before the measurements are recorded. A new header is also printed when there is a date change at midnight.• Each NBP measurement is recorded. The time when the measurement ended is recorded.• Each Temperature measurement is recorded. The time when the measurement ended is recorded.• Other maternal parameters (SpO2, maternal heart rate or Pulse) are recorded every five minutes. The rules described in the section “Priority for Maternal Heart / Pulse Rate” on page 223 apply.• Paper Save Mode recording stops if there are no valid maternal measurements for more than one hour, and a message will notify you that there are no active parameters. Paper Save Mode recording will restart automatically when another valid measurement is made.Event Paper Save Mode ReactivationOne of the maternal measurements (see above) is valid again. yesThe recorder is turned on and off again or a report has been recorded (e.g. NST Report).yesThe Paper Advance function is used. yesThe Paper Save Mode setting is set off and on again. yesADT information has changed (e.g. because patient information has been completed or updated).noThe monitor is restarted (e.g. by switching it off and on again). yesThe date has changed (e.g. at midnight). no
23 Paper Save Mode for Maternal Measurements240
2424124Recovering DataThe monitor stores trace data, including annotations, in its internal backup memory. This allows the monitor to recover trace data that would otherwise be lost under certain circumstances. This trace recovery data can be automatically retrieved and printed in the event of the paper running out, or automatically transmitted to an OB TraceVue/IntelliSpace Perinatal system (LAN connection only), allowing continuity of data.The fetal trace printed from the trace recovery data contains all data from the real-time trace, with the exception of the maternal heart rate, the pulse numeric and the MECG wave.Note that the data in the memory is cleared when a software upgrade is performed.CAUTIONOnly use Philips paper. Using paper other than Philips paper may result in the failure to recover traces.Recovering Traces on PaperThe monitor is able to recover traces by printing them out at a high speed from the monitor's backup memory. If the monitor runs out of paper, or if the paper drawer is open, the exact time when this happens is annotated in the backup memory. If the Bridge Paperout setting is set to On (default), when new paper is loaded and the recorder is started, a trace recovery printout of the data recovered from the backup memory is automatically printed out at high speed (up to 20 mm/s), starting from the time noted in the backup memory. This ensures that no data is lost. A minimum of one hour of trace recovery data can be printed out from the backup memory. When the trace recovery printout has finished, the recorder automatically switches back to continue recording the current trace at the normal speed.Note the following:• If you press the fetal recorder Start/ Stop SmartKey during a trace recovery printout, the recording stops and the next recording following a recorder restart will be a normal, real-time trace.After switching the monitor off and then back on again, or following a power failure, the time of the last Check Paper INOP or paper-out detection is lost, and therefore any trace recovery data in the backup memory is no longer available to print. The next recording made following a restart of the recorder is a normal, real-time trace.
24 Recovering Data242• The change back to a real-time recording from a trace recovery printout prompts the recording to restart. A new vertical trace header annotation consisting of the time, date and paper speed is printed, letting you see where the trace recovery printout ends, and where the real-time trace continues.• There can be a gap of up to 30 seconds between the trace recovery printout and the beginning of the real-time trace.Recovering Traces on an OB TraceVue/IntelliSpace Perinatal SystemThe trace recovery data stored in the monitor's backup memory can also be uploaded at high speed to an OB TraceVue/IntelliSpace Perinatal system connected over the LAN interface (OB TraceVue Revision E.00.00 or later, and IntelliSpace Perinatal H.0 or later).When the OB TraceVue/IntelliSpace Perinatal system reconnects to the fetal monitor and detects that there is trace recovery data in the monitor's backup memory that has not yet been transmitted to the system, this data is transferred at high speed to the system. No user action is required.The exact length of the recovered trace will vary depending on the amount of trace information, but will cover at least one hour of trace data, regardless of how many parameters are being measured.To recover traces on an OB TraceVue/IntelliSpace Perinatal system, the following applies:• The trace data in the monitor's internal memory must relate to a specific patient in the OB TraceVue/IntelliSpace Perinatal system. In other words, there were no discharge events made on the monitor that would change the patient context.• The patient must have an open episode. No data will be uploaded if the patient is not admitted to OB TraceVue/IntelliSpace Perinatal. For this reason, it is not possible to use the monitor to collect patient data offline for later transmission to OB TraceVue/IntelliSpace Perinatal.• Current online trace data is held back until the fast upload is complete.Recording Stored DataIf the recorder is not running, you can choose to print trace data from the monitor's memory at any time. You can see a list of all stored traces, showing patient identification and trace period, in the Stored Data Recording window, from which you can choose one entry at a time.CAUTIONEnsure that you admit each patient by name, including other patient identification information, and discharge the patient when you have finished monitoring, so that you can identify which trace period (entry in the patient list) refers to which patient. Trace storage can be triggered by:• Discharging a patient• Powering on the monitor•Entering Standby• Entering Service Mode
24 Recovering Data243Traces are not available for periods the monitor was switched off, in Service mode, in Standby, or if the trace period was shorter than one minute. To delete all stored trace periods press the Erase All key.The speed of the printout depends on the configured recorder speed and on the amount of trace data available. The fetal trace printed from the trace data contains all data from the real-time trace, with the exception of the maternal heart rate, the pulse numeric and the ECG wave.Information for scale type, trace separation and recorder speed are not stored in the trace memory, but is applied when the stored recording starts. While the stored recording is printing, all functions are disabled, except that for stopping the recorder.To start a stored data recording:Either1Select the Stored Data Rec SmartKey.Or1Enter the Main Setup menu using the SmartKey.2Select Fetal Recorder to open the Fetal Recorder menu.3Select Stored Data Rec to open the Stored Data Recording window.4Select an entry for a patient.5Select All to print all stored trace data for the selected entry, or select one of the choices on the other pop-up keys to print only a specified portion of the entry (for example, Last 15 min for the last 15 minutes of trace data).To delete all stored trace periods:Either1Select the Stored Data Rec SmartKey.Or1Enter the Main Setup menu using the SmartKey.2Select Fetal Recorder to open the Fetal Recorder menu.3Select Stored Data Rec to open the Stored Data Recording window.4Select the Erase All key to delete all stored trace periods listed.5Select the Confirm key. The current patient’s entry is at the top of the list. The oldest entry at the bottom of the list has no start time specified, as part of the data originally stored may have been over-written by the current patient’s data. The first part of the data, including the information for the start time, is no longer accessible.
24 Recovering Data244It may be that you only see one entry (the current patient’s data) in the Stored Data Recording window if that patient was monitored for a period long enough to erase any earlier entries.If you make a stored data recording for an old entry (that is, not for the current patient), the recorder performs a fast trace printout of the stored data, advances the paper to the next paper fold, then stops.If you make a stored data recording for the current patient, the recorder performs a fast trace printout of the stored data, and then reverts automatically to recording the real-time trace.
2524525Care and CleaningUse only the Philips-approved substances and methods listed in this chapter to clean or disinfect your equipment. Warranty does not cover damage caused by using unapproved substances or methods.Philips makes no claims regarding the efficacy of the listed chemicals or methods as a means for controlling infection. Consult your hospital’s Infection Control Officer or Epidemiologist. For comprehensive details on cleaning agents and their efficacy refer to “Guideline for Disinfection and Sterilization in Healthcare Facilities” issued by the U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control, Atlanta, Georgia, 2008. See also any local policies that apply within your hospital, and country.General PointsThe transducers and patient modules are sensitive instruments. Handle them with care.Keep your monitor, transducers, patient modules, cables and accessories free of dust and dirt. After cleaning and disinfection, check the equipment carefully. Do not use if you see signs of deterioration or damage. If you need to return any equipment to Philips, always decontaminate it first before sending it back in appropriate packaging.Observe the following general precautions:• Always follow carefully and retain the instructions that accompany the specific cleaning and disinfecting substances you are using.• Always dilute according to the manufacturer's instructions or use lowest possible concentration.• Do not allow liquid to enter the case.• Do not immerse the monitor in liquid. Protect it against water sprays or splashes.• Do not pour liquid onto the system.• Never use abrasive material (such as steel wool or silver polish).• Never use bleach.
25 Care and Cleaning246WARNING• Do not operate the monitor if it is wet. If you spill liquid on the monitor, contact your service personnel or Philips service engineer.• Do not perform underwater monitoring (for example, in a bath or shower) using wired transducers.• Place the monitor where there is no chance of contact with, or falling into water or other liquid.• Do not dry equipment using heating devices such as heaters, ovens (including microwave ovens), hair dryers and heating lamps.• Do not put equipment or accessories in autoclave (for sterilization).Cleaning and DisinfectingClean and disinfect the Avalon FM20, FM30, FM40 and FM50 fetal monitors and the transducers M2734A, M2734B, M2735A, M2736A, and M2738A (including ECG adapter cables) and the Avalon CL base station and the cableless transducers after each use. Clean equipment before disinfecting. For other accessories, see “Cleaning and Disinfecting Monitoring Accessories” on page 247.Clean with a lint-free cloth, moistened with warm water (40°C/104°F maximum) and soap, a diluted non-caustic detergent, tenside, or phosphate based cleaning agent (see “Recommended Disinfectants” on page 247). Do not use strong solvents such as acetone or trichloroethylene. After cleaning, disinfect using only the approved disinfecting agents listed.CAUTIONSolutions: Do not mix disinfecting solutions (such as bleach and ammonia) as hazardous gasses may result.Skin contact: To reduce the risk of skin irritations, do not allow a cleaning or disinfecting agent to leave residues on any of the equipment surfaces - wipe it off with a cloth dampened with water, after allowing the appropriate time for the agent to work, or before applying to a patient.Hospital policy: Disinfect the product as determined by your hospital's policy, to avoid long term damage to the product.Local requirements: Observe local laws governing the use of disinfecting agents.Touch display: To clean and disinfect the touch-enabled display, disable the touch operation by switching off the monitor during the cleaning procedure, or by selecting and holding the Main Screen key until the padlock symbol appears on it, indicating that touch operation is disabled. Select and hold again to re-enable touch operation.Take extra care when cleaning the screen of the monitor because it is more sensitive to rough cleaning methods than the housing. Do not permit any liquid to enter the monitor case and avoid pouring it on the monitor while cleaning. Do not allow water or cleaning solution to enter the measurement connectors. Wipe around and not over connector sockets, or those of the Toco+, CL Toco transducer, ECG and IUP Patient Modules, CL ECG/IUP transducer and adapter cables.Wash soiled reusable belts with soap and water. Water temperature must not exceed 60°C/140°F.
25 Care and Cleaning247Recommended DisinfectantsWe recommend that you use one of the following disinfectants:Cleaning and Disinfecting Monitoring AccessoriesTo clean, disinfect and sterilize reusable transducers, sensors, cables, leads, and so forth, refer to the instructions delivered with the accessory.Do not allow a cleaning or disinfecting agent to leave residues on any of the equipment surfaces. Wipe residues off, after allowing the appropriate time to for the agent to work, with a cloth.Product Name Product Type IngredientsIsopropanol liquid Isopropanol 80%Bacillol® AF liquid, spray 100 g concentrate contains:Propan-1-ol 45.0 g; Propan-2-ol 25.0 g; Ethanol 4.7 g.Bacillol®25 liquid Ethanol 100 mg/gPropan-2-ol (= 2-Propanol) 90 mg/g; Propan-1-ol (= 1-Propanol) 60 mg/gMeliseptol® spray 50% 1-PropanolAccel TB RTU liquid 0.5% accelerated hydrogen peroxideOxivir® Tb Cleaner Disinfectant spray 0.5% accelerated hydrogen peroxideOxivir® Tb Wipes wipes 0.5% accelerated hydrogen peroxideCarpe DiemTM/MC TbReady-to-Use General Virucide, Bactericide, Tuberculocide, Fungicide, Sanitizerspray 0.5% accelerated hydrogen peroxideCarpe DiemTM/MC Tb Wipes wipes 0.5% accelerated hydrogen peroxideSuper Sani-ClothGermicidal Disposable Wipeswipes isopropanol 55%quaternary ammonium chlorides 0.5%SANI-CLOTH® PLUSGermicidal Disposable Wipeswipes isopropanol 15%quaternary ammonium chlorides 0.25%SANI-CLOTH® HB GermicidalGermicidal Disposable Wipeswipes isopropanol < 0.15%quaternary ammonium chlorides 0.14%
25 Care and Cleaning248Cleaning and Disinfecting the Tympanic Temperature AccessoriesProbe and Thermometer Body1Wipe the thermometer body clean with a damp cloth. The water temperature should not exceed 55°C (130°F). Do not soak, rinse, or submerge the thermometer under water.You may add a mild detergent to the water. 2Clean the probe tip with a lint free swab. If the probe tip is soiled, clean it with a dampened swab. 3After you have removed all foreign matter, clean the thermometer lens at the end of the probe tip with a lint free swab or lens wipe. The thermometer lens must be free from fingerprints and/or smudges for proper operation.4Thoroughly dry all surfaces before using the equipment.CAUTIONDo not use cleaners and disinfectants such as Spray-Nine™*, Phisohex™*, Hibiclens™*, or Vesta-Syde™* as they may result in damage to the thermometer case.Occasional use of a 10:1 water and hypochlorite mixture or a damp isopropyl alcohol wipe or Cidex™* or ManuKlenz™* or VIROX™* or CaviWipes™* cleansing agents is acceptable, however, prolonged or repeated use of these chemicals may result in damage to the thermometer case and display area.Use of a cloth or sponge is recommended for cleaning. Never use an abrasive pad or an abrasive cleaner on the thermometer.The thermometer is non-sterile. Do not use ethylene oxide gas, heat, autoclave, or any other harsh method to sterilize this thermometer.SterilizingSterilization is not recommended for this monitor, related products, accessories or supplies unless otherwise indicated in the Instructions for Use that accompany the accessories and supplies.WARNINGDo not put device and accessories in autoclave (for sterilization).
26 Maintenance24926MaintenanceWARNINGSchedule: Failure on the part of the responsible individual hospital or institution employing the use of this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards.In case of problems: If you discover a problem with any of the equipment, contact your service personnel, Philips, or your authorized supplier.Electric shock hazard: Do not open the monitor housing. Refer all servicing to qualified service personnel.Inspecting the Equipment and AccessoriesYou should perform a visual inspection before each use, and in accordance with your hospital's policy. With the monitor switched off:1Examine unit exteriors for cleanliness and general physical condition. Make sure that the housings are not cracked or broken, that everything is present, that there are no spilled liquids that may have entered the housing, and that there are no signs of abuse.2Inspect all accessories (transducers, sensors and cables, and so forth). Do not use a damaged accessory.3Avoid frequent drops of the transducers. 4Switch the monitor on and make sure the display is bright enough. If the brightness is not adequate, contact your service personnel or your supplier.Batteries Preventive MaintenanceFor the FM20/30 with a battery option refer to “Using Batteries” on page 102.Inspecting the Cables and Cords1Examine all system cables, the power plug and cord for damage. Make sure that the prongs of the plug do not move in the casing. If damaged, replace it with an appropriate power cord.2Inspect the cables, leads and their strain reliefs for general condition. Make sure there are no breaks in the insulation. Make sure that the connectors are properly engaged at each end to prevent rotation or other strain.3Carry out performance assurance checks as described in the monitor's Service Guide.
26 Maintenance250Maintenance Task and Test ScheduleThe following tasks are for Philips-qualified service professionals. All maintenance tasks and performance tests are documented in detail in the service documentation supplied on the monitor's documentation DVD.Ensure that these tasks are carried out as indicated by the monitor's maintenance schedule, or as specified by local laws, whichever comes sooner. Contact a Philips-qualified service professionals if your monitor needs a safety or performance test. Clean and disinfect equipment to decontaminate it before testing or maintaining it.Recorder MaintenanceRemoving the Paper Guide: FM40/FM50FM40/50 The paper guide is removable, and you can use the recorder without it. When not using the paper guide, ALWAYS tear off the paper along the perforation to avoid possible paper misalignment (see “Tearing Off the Paper” on page 80).Maintenance and Test Schedule FrequencyVisual Inspection Before each use.Clean and disinfect the equipment After each use.Safety checks according to IEC 60601-1, and where applicable, to national standardsAt least once every two years, or as specified by local laws.After any repairs where the power supply has been replaced (by an authorized service professional).If the monitor has been dropped, it must be repaired/checked by an authorized service agent.Performance assurance for all measurementsAt least once every two years, or if you suspect the measurement values are incorrect.Noninvasive blood pressure calibration At least once every two years, or as specified by local laws.Clean the thermal printhead At each paper pack change, or every 500 m of paper run.
26 Maintenance251To remove the paper guide:1Press the paper eject button to open the paper drawer.2Hinge the transparent paper guide forward.
26 Maintenance252AProtrusion holds paper guide in closed position.3Release the paper guide from one side of the holder.
262534Then remove the paper guide.Refitting is a reversal of the removal procedure.
26 Maintenance254Storing Recorder PaperRecorder paper is not intended for long-term archival storage. Another medium should be considered if this is required.Dyes contained in thermal papers tend to react with solvents and other chemical compounds that are being used in adhesives. If these compounds come into contact with the thermal print, the print may be destroyed over time. You can take the following precautionary measures to help avoid this effect:• Store the paper in a cool, dry and dark place.• Do not store the paper at temperatures over 40°C (104°F).• Do not store the paper where the relative humidity exceeds 60%.• Avoid intensive light (UV light), as this may cause the paper to turn gray or the thermal print to fade.• Avoid storing the thermal paper in combination with the following conditions:– Papers that contain organic solvents. This includes papers with tributyl and/or dibutyl phosphates, for example recycled paper.– Carbon paper and carbonless copy paper.– Products containing polyvinyl chlorides or other vinyl chlorides for example (but not exclusively) document holders, envelopes, letter files, divider sheets.– Detergents and solvents, such as alcohol, ketone, ester and others, including cleaning and disinfecting agents.– Products containing solvent-based adhesives such as (but not exclusively) laminating film, transparent film or labels sensitive to pressure.To ensure long lasting legibility and durability of thermal printouts, store your documents separately in an air-conditioned place and use:• only plasticizer-free envelopes or divider sheets for protection.• laminating films and systems with water-based adhesives.Using such protective envelopes cannot prevent the fading effect caused by other, external agents.
26 Maintenance255Cleaning the Print HeadTo clean the recorder's thermal print-head:FM20/301Switch off the monitor.2Open the paper drawer, and remove the paper if necessary, to gain access to the thermal print head.3Gently clean the thermal print head with a cotton swab or soft cloth soaked in isopropyl alcohol.FM40/50
26 Maintenance256Disposing of the MonitorWARNINGTo avoid contaminating or infecting personnel, the environment or other equipment, make sure you disinfect and decontaminate the monitor appropriately before disposing of it in accordance with your country's laws for equipment containing electrical and electronic parts. For disposal of parts and accessories such as thermometers, where not otherwise specified, follow local regulations regarding disposal of hospital waste.You can disassemble the monitor and the transducers as described in the Installation and Service Manual. You will find detailed disposal information on the following web page: http://www.healthcare.philips.com/main/about/Sustainability/Recycling/pm.wpdThe Recycling Passports located there contain information on the material content of the equipment, including potentially dangerous materials which must be removed before recycling (for example, batteries and parts containing mercury or magnesium).Do not dispose of waste electrical and electronic equipment as unsorted municipal waste. Collect it separately, so that it can be safely and properly reused, treated, recycled, or recovered.
27 Accessories and Supplies25727Accessories and SuppliesAll accessories listed for the fetal monitor may not be available in all geographies. You can order parts, accessories and supplies from Philips supplies at www.healthcare.philips.com or consult your local Philips representative for details. All accessories and supplies listed here are reusable, unless indicated otherwise.WARNINGReuse: Disposable accessories and supplies intended for single use, or single patient use only, and are indicated as such on their packaging. Never reuse disposable accessories and supplies, such as transducers, sensors, electrodes and so forth that are intended for single use, or single patient use only.Approved accessories: Use only Philips-approved accessories.Packaging: Do not use a sterilized accessory if its packaging is damaged.Protection against electric shocks: The transducers and accessories listed in this chapter are not defibrillator proof.Electro-Surgery, Defibrillation and MRI: The fetal/maternal monitors are not intended for use during defibrillation, electro-surgery, or MRI. Remove all transducers, sensors, and accessories before performing electro-surgery, defibrillation, or MRI, otherwise harm can result.Information on LatexAll Philips transducers and accessories are latex-free, unless indicated otherwise in the following tables.
27 Accessories and Supplies258Avalon CL Base StationTransducersFetal AccessoriesCL Base Station Part NumberAvalon CL Base Station can either be ordered with the option K30 (red connector) or K40 (black connector)866074Transducer Part NumberAvalon Toco Transducer M2734AAvalon Toco+ Transducer for Toco, DECG, MECG or IUP monitoring M2735AAvalon Toco MP Transducer for Toco and Maternal Pulse M2734BAvalon Ultrasound Transducer M2736AAvalon Ultrasound Transducer USA M2736AAECG/IUP Patient Module (for DECG, MECG or IUP) M2738AAvalon CL Toco+ MP Transducerfor use with the Avalon CL base station866075Avalon CL Ultrasound Transducerfor use with the Avalon CL base station866076Avalon CL ECG/IUP Transducerfor use with the Avalon CL base station866077Connector Caps for Avalon CL Cableless Smart Transducers (kit of 10)for use with the Avalon CL Toco+ MP transducer989803184841Belt Clip for Avalon CL Cableless Smart Transducers (kit of 10) 989803184851CL SpO2 Podfor use with the Avalon CL base station865215CL NBP Podfor use with the Avalon CL base station865216Remote Event Marker 989803143411Accessory Description Part NumberBelt(reusable, gray, water resistant)32 mm wide, 15 m roll M4601A160 mm wide, 5 belts M4602A60 mm wide, 15 m roll M4603A50 mm wide, 5 belts M1562B
27 Accessories and Supplies259Belt(reusable, brown, contains latex)32 mm wide, 15 m roll 1500-0628150 mm wide, 5 belts M1562A60 mm wide, 5 belts 1500-064260 mm wide, 15 m roll 1500-0643Belt(disposable, yellow, water resistant)60 mm wide, pack of 100 M2208AUltrasound gel 12 Bottles 40483A5 liter refill (with dispenser) for 40483AShelf life: 24 months max.40483BBelt buttons (kit of 10) M1569AButterfly belt clip (kit of 6) 989803143401Avalon CL Connector Caps Connector Caps for Avalon CL Cableless Smart Transducers (kit of 10)989803184841Avalon CL Belt Clip Belt Clip for Avalon CL Cableless Smart Transducers (kit of 10)989803184851Avalon CL Battery Replacement Kit 989803184861Cable Management Kit 989803148841Belt Clips for Avalon Smart Transducers (kit of 6) 989803143401DECG Accessories:New Philips DECG Solution(NOT compatible with QwikConnect Plus Solution accessories)DECG reusable legplate adapter cable (with flushing port)989803137651DECG leg attachment electrode for DECG legplate adapter cable 989803139771DECG fetal scalp electrode: single spiral, worldwide availability989803137631DECG fetal scalp electrode: double spiral, Europe only. Not for USA989803137641Disposable Koala IUP catheter M1333AReusable Koala IUP adapter cable 989803143931Accessory Description Part Number
27 Accessories and Supplies260DECG Accessories: Component CompatibilityUse the following pictorial guide to check component compatibility for DECG accessories.CAUTIONDo not mix accessories from the New Philips DECG Solution (marked 1) with those from the QwikConnect Plus Solution (marked 2).MECG AccessoriesNoninvasive Blood Pressure AccessoriesThe following accessories are approved for use with the fetal monitor:Accessory Part NumberMECG reusable adapter cable M1363AFoam ECG electrodes, snap-fit, for MECG Adapter Cable (disposable) 40493D/E
27 Accessories and Supplies261Adult Multi-Patient Comfort Cuffs and Disposable CuffsAdult EasyCare Reusable CuffsMaternal Patient CategoryLimb Circumference Bladder WidthDisposable cuffPart No.Reusable cuffPart No.TubingAdult (Thigh) 42.0 - 54.0 cm 20.0 cm M1879A M1576A M1598B (1.5 m)orM1599B (3.0 m)Large Adult 34.0 - 43.0 cm 16.0 cm M1878A M1575AAdult 27.0 - 35.0 cm 13.0 cm M1877A M1574ASmall Adult 20.5 - 28.0 cm 10.5 cm M1876A M1573ACuff kit of 4 adult sizesM1578AMaternal Patient Category (color) Limb Circumference Bladder WidthPart No. TubingAdult Thigh (grey) 45.0 - 56.5 cm 21.0 cm M4559B M1598B (1.5 m)orM1599B (3.0 m)Adult Thigh (grey) pack of 5 cuffs 45.0 - 56.5 cm 21.0 cm M4559B5Large Adult X-Long (burgundy) 35.5 - 46.0 cm 17.0 cm M4558BLarge Adult X-Long (burgundy) pack of 5 cuffs35.5 - 46.0 cm 17.0 cm M4558B5Large Adult (burgundy) 35.5 - 46.0 cm 17.0 cm M4557BLarge Adult (burgundy)pack of 5 cuffs35.5 - 46.0 cm 17.0 cm M4557B5Adult X-Long (navy blue) 27.5 - 36.5 cm 13.5 cm M4556BAdult X-Long (navy blue)pack of 5 cuffs27.5 - 36.5 cm 13.5 cm M4556B5Adult (navy blue) 27.5 - 36.5 cm 13.5 cm M4555BAdult (navy blue)pack of 5 cuffs27.5 - 36.5 cm 13.5 cm M4555B5Small Adult (royal blue) 20.5 - 28.5 cm 10.6 cm M4554BSmall Adult (royal blue)pack of 5 cuffs20.5 - 28.5 cm 10.6 cm M4554B5Cuff kits containing one small adult, one adult, one large adult and one thigh cuff.864288Cuff kits containing one small adult, one adult, one adult X-long, one large adult, one large adult X-long and one thigh cuff864291
27 Accessories and Supplies262Adult Single Patient Soft CuffsIntelliVue CL NBP Pod AccessoriesMaternal Patient Category Limb Circumference Bladder Width Part No. TubingAdult (Thigh) 45.0 - 56.5 cm 20.4 cm M4579B M1598B (1.5 m)orM1599B (3.0 m)Large Adult X-Long 35.5 - 46.0 cm 16.4 cm M4578BLarge Adult 35.5 - 46.0 cm 16.4 cm M4577BAdult X-Long 27.5 - 36.5 cm 13.1 cm M4576BAdult 27.5 - 36.5 cm 13.1 cm M4575BSmall Adult 20.5 - 28.5 cm 10.4 cm M4574BDescription Limb Circumference RangeBladder Width Contents Product No.Mobile CL Reusable Small Adult Cuff21 - 27 cm 10.5 cm 1 cuff 989803163171Mobile CL Reusable Adult Cuff 26.0 - 34.5 cm 13.0 cm 1 cuff 989803163191Mobile CL Reusable Large Adult Cuff33.5 - 45.0 cm 16.0 cm 1 cuff 989803163211Mobile CL Single-Patient Small Adult Cuff21 - 27 cm 10.5 cm 20 cuffs 989803163181Mobile CL Single-Patient Adult Cuff26.0 - 34.5 cm 13.0 cm 20 cuffs 989803163201Mobile CL Single-Patient Large Adult Cuff33.5 - 45.0 cm 16.0 cm 20 cuffs 989803163221Mobile CL NBP Cradle Kit - - 20 cradles 989803163251Mobile CL Extension Air Hose, 1.0 m- - 1 extension air hose 989803163131Mobile CL NBP Battery Kit - - 1 Battery1 disassembly tool1 front housing989803163261Telemetry Pouch with window - - 50 pouches 989803137831Telemetry Pouch with window - - 4 boxes of 50 pouches989803140371White Telemetry Pouch with Snaps; box of 50- - 50 pouches 989803101971(9300-0768-050)White Telemetry Pouch with Snaps; 4 boxes of 50--4boxes of 50 pouches989803101981(9300-0768-200)
27 Accessories and Supplies263SpO2 AccessoriesSome Nellcor sensors contain natural rubber latex which may cause allergic reactions. See the Instructions for Use supplied with the sensors for more information. M1901B, M1903B and M1904B are not available in USA from Philips. Purchase Nellcor OxiCliq sensors and adapter cables directly from Tyco Healthcare. Some sensors may not be available in all countries.Do not use more than one extension cable with any sensors or adapter cables. Do not use an extension cable with Philips reusable sensors or adapter cables with part numbers ending in -L (indicates "Long" version).All listed sensors operate without risk of exceeding 41°C on the skin if ambient temperature is below 37°C.Make sure that you use only the accessories that are specified for use with this device, otherwise patient injury can result.Philips SpO2 AccessoriesDescription Comments Product NumberPhilips reusable sensorsAdult sensor (2.0 m cable), for patients over 50 kg. Any finger, except thumb.No adapter cable required. M1191BM1191A with longer cable (3.0 m) M1191BLSmall adult, pediatric sensor (1.5 m cable) for patients between 15 kg and 50 kg. Any finger except thumb.Use only on adult patients with FM30/40/50.M1192AEar sensor (1.5 m cable) for patients more than 40 kg.Use only on adult patients with FM30/40/50.M1194AAdult clip sensor (3 m cable) for patients over 40 kg. Any finger except thumb.M1196AAdult clip sensor (2 m cable) for patients over 40 kg. Any finger except thumb.M1196SAdult sensor (0.45 m), for patients over 50 kg. Any finger except thumb.Requires M1943A (1.0 m) or M1943AL (3.0 m) adapter cable.M1191TSmall adult, pediatric sensor (0.45 m cable) for patients between 15 kg and 50 kg. Any finger except thumb.Use only on adult patients with FM30/40/50.M1192TAdult clip sensor (0.9 m cable) for patients over 40 kg. Any finger except thumb.M1196T
27 Accessories and Supplies264Special Edition (SE)Adult sensor (3 m cable), for patients over 50 kg. Any finger except thumb.No adapter cable required.SE sensors work with FM30/40/50, as well as with OxiMax-compatible SpO2 versions of other Philips monitors.M1191ANLSpecial Edition (SE)Small adult, pediatric sensor (1.5 m cable) for patients between 15 kg and 50 kg. Any finger except thumb.Use only on adult patients with FM30/40/50.M1192ANSpecial Edition (SE)Ear sensor (1.5 m cable) for patients more than 40 kg.M1194ANPhilips disposable sensors. Not available in the USA.Identical to OxiMax MAX-A Requires M1943A (1.0 m) or M1943AL (3.0 m) adapter cableM1904BIdentical to OxiMax MAX-P M1903BIdentical to OxiMax MAX-N M1901BPhilips disposable sensors. Available worldwide.Adult/Pediatric finger sensor (0.45 m cable)Use only on adult patients with FM30/40/50.Requires M1943A (1.0 m) or M1943AL (3.0 m) adapter cableM1131AAdult/Infant/Neonatal (0.9 m cable) for patients > 40 kg. Any finger except thumb.Use only on adult patients with FM30/40/50.M1133AAdult/Infant/Neonatal (0.9 m cable) for patients > 40 kg. Any finger except thumb. Adhesive-freeUse only on adult patients with FM30/40/50.M1134ADescription Comments Product Number
27 Accessories and Supplies265Nellcor SpO2 AccessoriesMasimo SpO2 AccessoriesProduct Number Description CommentsNELLCOR disposable sensors (must be ordered from Nellcor)OxiMax MAX-A Adult finger sensor (patient size > 30 kg) Requires M1943A (1.0 m) or M1943AL (3.0 m) adapter cable.OxiMax MAX-AL OxiMax MAX-A with long cableOxiMax MAX-P Pediatric foot/hand sensor (patient size 10-50 kg)Use only on adult patients with FM30/40/50.OxiMax MAX-N Adult finger or neonatal foot/hand sensor(patient size > 40 kg or < 3 kg)Use only on adult patients with FM30/40/50.Oxisensor II D-25 Adult sensor (patient size > 30 kg) Requires M1943A (1.0 m) or M1943AL (3.0 m) adapter cable.Oxisensor II D-20 Pediatric sensor (patient size 10-50 kg)Use only on adult patients with FM30/40/50.Oxisensor II N-25 Neonatal/Adult sensor (patient size < 3 kg or > 40 kg) Use only on adult patients with FM30/40/50.OxiCliq A See OxiMax MAX-A Requires M1943A (1.0 m) or M1943AL (3.0 m) adapter cable together with OC3 adapter cable.OxiCliq P See OxiMax MAX-PUse only on adult patients with FM30/40/50.OxiCliq N See OxiMax MAX-NUse only on adult patients with FM30/40/50Product Number Description Philips Part NumberMASIMO LNOP reusable sensors (No adapter cable required)LNOP DC-I Adult Finger Sensor (> 30 kg) 989803140321LNOP DC-IP Pediatric Finger Sensor (10 - 50 kg)Use only on adult patients with FM30/40/50989803140331LNOP YI Multi-Site Sensor (> 1kg)Use only on adult patients with FM30/40/50n/aLNOP TC-I Ear Sensor (> 30 kg)Use only on adult patients with FM30/40/50989803140341MASIMO LNCS reusable sensors (No adapter cable required)LNCS DC-I Adult Finger Sensor (> 30 kg) 989803148281LNCS DC-IP Pediatric Finger Sensor (10 - 50 kg)Use only on adult patients with FM30/40/50989803148291LNCS TC-I Ear Sensor (> 30 kg)Use only on adult patients with FM30/40/50989803148301MASIMO LNOP disposable adhesive sensorsLNOP Adt Adult Sensor (> 30 kg) 989803140231
27 Accessories and Supplies266IntelliVue CL SpO2 Pod AccessoriesAll listed sensors operate without risk of exceeding 41°C on the skin, if the initial skin temperature does not exceed 35°C.Ensure that you use only the accessories that are specified for use with this device, otherwise patient injury can result.1 May not be available in all geographiesLNOP Adtx Adult Sensor (> 30 kg) n/aLNOP Pdt Pediatric Sensor (10 - 50 kg)Use only on adult patients with FM30/40/50989803140261LNOP Pdtx Pediatric Sensor (10 - 50 kg)Use only on adult patients with FM30/40/50n/aLNOP Neo-L Neonatal Sensor (< 3kg)or Adult adhesive Sensor (> 40 kg)Use only on adult patients with FM30/40/50989803140291MASIMO LNCS disposable adhesive sensors (No adapter cable required)LNCS Adtx Adult Sensor (> 30 kg) 989803148231LNCS Pdtx Pediatric Finger Sensor (10 - 50 kg)Use only on adult patients with FM30/40/50989803148241LNCS Neo-L Neonatal Foot Sensor (<3 kg)or Adult Finger Sensor (>40 kg)Use only on adult patients with FM30/40/50989803148271Product Number Description Philips Part NumberDescription Contents Product No.Mobile CL 20 single patient SpO2 Sensors and Cradles for use on adult patients >10 kg20 Single-Patient Mobile CL DSpO2-1A Sensors20 Single-Patient Wristbands20 Single-Patient Cradlespre-assembled989803165941Mobile CL 20 single patient SpO2 Sensors for use on adult patients > 10 kg20 Single-Patient Mobile CL DSpO2-1A Sensors 989803165921Mobile CL reusable SpO2 sensor and Cradles for use on adult patients > 15 kg1 Reusable Mobile CL RSpO2-1A Sensor20 Single-Patient Cradles with pre-attached Wristbands9898031659311Mobile CL 20 SpO2 Cradles (single patient) 20 Single-Patient Cradles with pre-attached Wristbands989803165951Mobile CL 50 SpO2 Wristbands (single patient)50 Single-Patient Wristbands 989803165961Mobile CL SpO2 Battery Kit 1 Battery1 disassembly tool1 front housing989803168861
27267Extension / Adapter CablesTympanic Temperature AccessoriesRecorder PaperSupplied in cases of 40 packs. Each pack has 150 numbered pages. Single use. Use the paper specified here.* Bradycardia and tachycardia alarm ranges are shaded.Description Comments Product No.Extension cable (2 m) For use with Philips reusable sensors and adapter cables. M1941AAdapter cable (1.1 m cable) Adapter cable for Philips/Nellcor disposable sensors. M1943AAdapter cable (3 m cable) M1943ALAdapter Cable for OxiCliq sensorsAvailable from Nellcor. OC 3LNOP MP12 LNOP MP Series Patient Cable (3.6 m) Adapter Cable for Masimo LNOP sensorsM1020-61102LNC MP10 LNCS MP Series Patient Cable (3.0 m) Adapter Cable for Masimo LNCS sensors989803148221Description Part No.Temperature probe 989803180831Disposable probe cover with CE marking (22 boxes @ 96) 989803179611Disposable probe cover (22 boxes @ 96) 989803179381Geography FHR Scale Grid Color Scale UnitsHighlighted 3cm Lines?Product No.USA/Canada and Asia 30 - 240 Red/Orange mmHg Yes M1910AEurope/Japan 50 - 210 Green mmHg and kPaNo M1911AJapan 50 - 210 Green mmHg Yes M1913AJapan 50 - 210 Green*mmHg Yes M1913J
27 Accessories and Supplies268BatteriesDescription Comment Product No.Smart Battery 10.8 V, 6000 mAh, Lithium IonFor Avalon FM20 or Avalon FM30 with battery option #E25M4605AAvalon CL Cableless Smart transducer Battery Replacement KitConsists of one Philips Lithium Ion Battery (Part No. 453564107871), a tool to open and close the cableless transducer for battery replacement and two replacement O-ring seals.989803184861
28 Specifications and Standards Compliance26928Specifications and Standards ComplianceThe monitors are intended to monitor a mother and her fetus(es), which from an electrical safety point of view, are one person.Environmental SpecificationsThe monitor may not meet the given performance specifications if stored and used outside the specified temperature and humidity ranges.Avalon CL Base station 866074Temperature Range Operating 0°C to 45°C (32°F to113°F)Storage/Transportation -20°C to 60°C (-4°F to 140°F)Humidity Range Operating <95% relative humidity @ 45°C/113°FStorage/Transportation <90% relative humidity @ 60°C/140°FAltitude Range Operating -500 to 3000 m/-1640 to 9840 ft.Storage/Transportation -500 to 13100 m/-1640 to 43000 ft.Monitor (M2702A/M2703A); Interface Cable for Avalon CTS (M2731-60001 and M2732-60001)Temperature Range Operating Without battery option: 0°C to 45°C (32°F to 113°F)With battery option/charging: 0°C to 35°C (32°F to 95°F)With battery option/fully charged: 0°C to 40°C (32°F to 104°F)Storage/Transportation -20°C to 60°C (-4°F to 140°F)Humidity Range Operating <95% relative humidity @ 40°C/104°FStorage/Transportation <90% relative humidity @ 60°C/140°FAltitude Range Operating -500 to 3000 m/-1640 to 9840 ft.Storage/Transportation -500 to 13100 m/-1640 to 43000 ft.Transducers (M2734A/M2734B/M2735A/M2736A/M2738A)Temperature Range Operating 0°C to 40°C (32°F to 104°F)Storage/Transportation -20°C to 60°C (-4°F to 140°F)Humidity Range Operating <95% relative humidity @ 40°C/104°FStorage/Transportation <90% relative humidity @ 60°C/140°F
28 Specifications and Standards Compliance270WARNINGExplosion Hazard: Do not use in the presence of flammable anesthetics, such as a flammable anesthetic mixture with air, oxygen, nitrous oxide, or in oxygen rich environment. Use of the devices in such an environment may present an explosion hazard.Altitude Range Operating -500 to 3000 m/-1640 to 9840 ft.Storage/Transportation -500 to 13100 m/-1640 to 43000 ft.Transducers (M2734A/M2734B/M2735A/M2736A/M2738A)Avalon CL Transducers (866075/866076/866077)Temperature Range Operating 0°C to 40°C (32°F to 104°F)Charging 0°C to 35°C (32°F to 95°F)Storage/Transportation -20°C to 60°C (-4°F to 140°F)Humidity Range Operating <95% relative humidity @ 40°C/104°FStorage/Transportation <90% relative humidity @ 60°C/140°FAltitude Range Operating -500 to 3000 m/-1640 to 9840 ft.Storage/Transportation -500 to 13100 m/-1640 to 43000 ft.SpO2 SensorsOperating Temperature Range 0°C to 37°C (32°F to 98.6°F)
28 Specifications and Standards Compliance271Physical SpecificationsAvalon CL Base StationDimension and Weight Size mm/(in):width x height x depth349 x 74 x 183 mm(349 mm-5% max. width 350 mm)(13.7 x 2.9 x 7.2 in13.7 in -5% max. width 13.8 in)Weight 0.985 kg /2.2 lbsElectrical Class When connected to M2702A/M2703A/M2704A/M2705A Class II equipment using a red connector at the fetal sockets.When connected to M2704A/M2705A Class I equipment using a black connector in the telemetry socket. Electrical Power Source External (powered by fetal monitor)Mode of Operation Continuous operationInterface cable connector type Connector color Red for FM20/30 left side or FM40/50 front fetal connector socketBlack for FM40/50 rear telemetry connector socketInterface cable length 1,5 m /4.11 ftIngress Protection IP31Monitor Physical Specifications M2702A/M2703A M2704A/M2705APower Supply Voltages 100 VAC to 240 VAC ±10%Supply Frequency Range 50 Hz/60 HzPower Consumption (current)0.7 - 0.4 A (M2702A/M2703A)1.3 - 0.7 A (M8023A#E25)1.3 - 0.7 ADimensions and WeightSize (without options) mm/(in):width x height x depth286 x 133 x 335 ±1%(11.3 x 5.2 x 13.2 in ±1%)420 x 172 x 370 ±5%(16.5 x 6.8 x 14.6 in ±5%)Weight < 5.1 kg/11.2 lbs < 9.0 kg/19.8 lbsDegree of Protection Against Electrical Shock Type CFElectrical Class Class II equipment Class I equipmentElectrical Power Source External (AC) without battery option #E25Internal (LiIo battery) if with battery option #E25External (AC)Mode of Operation Continuous operationWater Ingress Protection Code - IP X1 (provided recorder drawer is shut)
28 Specifications and Standards Compliance272Global Speed 6.25 mm/sec, 12.5 mm/sec, 25 mm/sec, 50 mm/secStartup Time Time taken from switching on the monitor to seeing the first parameter labels< 30 secondsMonitor Physical Specifications M2702A/M2703A M2704A/M2705ATransducers (M2734A/M2734B/M2735A/M2736A/M2738A)Shock Resistance Withstands a 1 m drop to concrete surface with possible cosmetic damage onlyWater Ingress Protection CodeM2734A&B/35/36A IP 68 (immersion up to 1 m water depth for 5 hours)M2738A IP 67 (immersion up to 0.5 m water depth for 30 minutes)Dimensions and WeightM2734A&B/35/36A Size (diameter) 83 mm/3.27 inWeight (without cable) < 220 g/7.8 oz.M2738A Maximum size mm/(in): width x height x depth50 x 28 x 135 (2.0 x 1.1 x 5.3 in)Cable length 2.5 mWeight < 150 g/5.3 oz.Degree of Protection Against Electrical Shock Type CFTransducer Identification Optical Signal Element (Finder LED). Not M2738AAvalon CL Transducers (866075/866076/866077)Shock Resistance Withstands a 1.5 m drop to concrete surface with possible cosmetic damage only.Water Ingress Protection Code IP 68 (immersion up to 1 m water depth for 5 hours)Dimensions and WeightAvalon Cableless Toco+MP Transducer 866075Size (diameter/height) 75.5 mm/ 36.6 mm2.9 / 1.4 inWeight 123 g ±10%/4.3 oz ±10%Avalon Cableless US Transducer 866076Size (diameter/height) 75.5 mm/ 36.6 mm2.9 / 1.4 inWeight 131 g ±10%/4.6 oz ±10%Avalon Cableless ECG/IUP Transducer 866077Size (diameter/height) 75.5 mm/ 36.6 mm2.9 / 1.4 inWeight 121 g ±10%/4.2 oz ±10%Degree of Protection Against Electrical Shock Type CFTransducer Identification Optical Signal Element (Finder LED).
28 Specifications and Standards Compliance273Interface Cable for Avalon CTS (M2731-60001 and M2732-60001)Shock Resistance Withstands a 1m drop to concrete surface with possible cosmetic damage onlyWater Ingress Protection Code IP X1Dimensions and Weight Maximum size mm/(in): width x height x depth55 x 28 x 50 (2.2 x 1.1 x 2.0 in)Cable length 2.5 mWeight < 200 g/7.0 oz.M8023A (Option #E25) External Power Supply Weight and DimensionsMaximum Weight 700 g ±10% (1.5 lb ±10%)Size (W x H x D) 207 x 70 x 113 mm / 8.1 x 2.8 x 4.4 inInterface SpecificationsNetwork Standard 100-Base-TX (IEEE 802.3 Clause 25)Connector RJ45 (8 pin)Isolation Basic insulation (reference voltage: 250 V; test voltage: 1500 V)MIB/RS232 Standard IEEE 1073-3.2-2000Connectors RJ45 (8 pin)Mode Software-controllableBCC (RxD/TxD cross over) orDCC (RxD/TxD straight throughPower 5 V ±5 %, 100 mA (max.)Isolation Basic insulation (reference voltage: 250 V; test voltage: 1500 V)USB Interface Standard USB 2.0 full-speed (embedded host)Connectors USB series "Standard A" receptaclePower Low power port 4.4V min; max. load for all ports together 500 mAIsolation noneRS232 (Standard) Connectors RJ45 (8-pin)Power noneInsulation Basic insulation (reference voltage: 250 V; test voltage: 1500 V)RS232 (Independent display interface option)Connectors RJ45 (8-pin)Power noneIsolation noneBasic Nurse Call Relay Connectors Modular Jack 6P6C, active open and closed contactContact <=100 mA, <=24 V DCIsolation Basic insulation (reference voltage: 250 V; test voltage: 1500 V)Delay <[Configured Latency +0.5] sec
28 Specifications and Standards Compliance2741 The power loss indication functionality of the Nurse Call Relay board is not supported with fetal monitors.Flexible Nurse Call Relay1Connectors 20 pin MDR (Mini D-Ribbon), active open and closed contactsContact <=100 mA, <=24 V DCIsolation Basic insulation (reference voltage: 250 V; test voltage: 1500 V)Delay <[Configured Latency +0.5] secInterface SpecificationsAvalon CL Radio Interface SpecificationsShort Range Radio Interface Type Internal SRR interfaceTechnology IEEE 802.15.4Frequency Band 2.4 GHz ISM (2.400 - 2.483 GHz)Modulation Technique DSSS (O -QPSK)Effective radiated power max. 0 dBm (1 mW)Range ca. 5 m without any physical obstructions as walls and doorsOBR (WMTS) Frequency Band 608 - 614 MHzEffective radiated power <20 mW (Base Station) <1 mW (CL transducers)Range min. 70 mOBR (ISM) Frequency Band 433.05 -434.79 MHzEffective radiated power <10 mW (Base Station)<1 mW (CL transducers)Range min. 70 mOBR (T108) Frequency Band 920.6 - 923.4 MHZEffective radiated power <20 mW (Base Station) <10 mW (CL transducers)Range min. 70 m
28 Specifications and Standards Compliance275Performance SpecificationsBattery SpecificationsFetal / Maternal SpecificationsPerformance SpecificationsAvalon FM20/30 Battery Option #E25Operating Time(with new, fully charged battery)Basic monitoring configuration: >2 hours(Display Brightness: 70%, Recorder: "On" at 3cm/min,NBP: Auto Mode at 15min, 2 US Transducers, 1 Toco+ with MECG, 1 Patient Module with DECG)Charge Time When monitor is off: approx. 6 hoursWhen monitor is in use: more than 10 hours (depending on monitor configuration).Performance SpecificationAvalon CL Transducer BatteryOperating time With a new and fully charged battery min. 8 hoursCharge time From a "low battery" indication to a "fully charged" indication min. 3 hoursPerformance SpecificationsUltrasoundMeasurement Method Ultrasound Pulse DopplerMeasurement Range US 50 to 240 bpmResolution Display 1 bpmPrinter 1/4 bpmJitter @ 200 bpm ≤ 3 bpmDisplay Update Rate 1 / secondUS Intensity (M2736A/AA) Average output power P = (7.4 ± 0.4) mWPeak-negative acoustic pressure p_ = (40.4 ± 4.3) kPaOutput beam intensity (Iob)(= spatial average - temporal average intensity)Isata = (2.38 ± 0.59) mW/cm2Spatial-peak temporal average intensity Ispta = (15.0 ± 3.2) mW/cm2Effective radiating area @ -12 dB (3.11 ± 0.74) cm2Thermal index (TI) and mechanical index (MI) are always below 1.0.
28 Specifications and Standards Compliance276US Intensity CL (866076) Average output power P = (12.4 ± 0.4) mWPeak-negative acoustic pressure p_ = (49.1 ± 5.2) kPaOutput beam intensity (Iob)(= spatial average - temporal average intensity)Isata = (2.77 ± 0.56) mW/cm2Spatial-peak temporal average intensity Ispta = (21.1 ± 5.1) mW/cm2Effective radiating area @ -12 dB A-12dB = (4.47 ± 0.89) cm2Thermal index (TI) and mechanical index (MI) are always below 1.0.Signal Quality Indication Poor Quality emptyAcceptable Quality half-fullGood Quality fullBeat-to -Beat (max.) for Ultrasound 28bmpUS Frequency 1 MHz ± 100 HzUS Signal range 3.5 µVpp to 350 µVpp @ 200 HzUS Burst Repetition Rate 3.0 kHzDuration ≤ 100 µsFMP Signal Range @ 33 Hz 200 µVpp to 40 µVppPerformance SpecificationsPerformance SpecificationsTocoMeasurement Method Strain Gauge Sensor ElementSensitivity 1 unit = 2.5 gResolution Display 1 unitPrinter 1/4 unitMeasurement Range 400 unitsSignal Range 0 to 127 unitsMaximum Offset Range -300 unitsBaseline Setting 20 unitsUpdate Rate Display 1 / secondPrinter ~4 / secondsAuto Offset Correction 3 seconds after connecting the transducer, the Toco value is set to 20 unitsAuto Zero Adjust Toco value is set to zero following a negative measurement value for 5 secondsPerformance SpecificationsMaternal Pulse from TocoEmitted Light Energy ≤ 15 mW
28 Specifications and Standards Compliance277Wavelength Range 780 to 1100 nmRange 40 to 240 bpmResolution 1 bpmDisplay Update Rate 1 / sAccuracy ± 2% or 1 bpm, whichever is greaterUpdate Rate every 4 secondsPerformance SpecificationsPerformance SpecificationsIUPMeasurement Method Passive Resistive Strain Gauge ElementsMeasurement Range -100 to +300 mmHgSignal Range -99 to 127 mmHg or -13.2 to 16.9 kPaResolution Display 1 mmHgPrinter 1/4 mmHgSensitivity 5 µV/V/mmHgOffset Compensation +100 to -200 mmHgAccuracy (not including sensor accuracy) ± 0.5% per 100 mmHgUpdate Rate Display 1 / secondPrinter ~4 / secondsAuto Offset Correction 3 seconds after connecting the transducer, the IUP value is set to 0 mmHgPerformance SpecificationsECGPerformance Specifications Type DECG Single Lead ECG (derived from Fetal Scalp Electrode)MECG Single Lead ECG (derived from RA and LA electrodes)Measurement Range 30 to 240 bpmResolution Display 1 bpm (display update rate 1/s)Recorder 1/4 bpmWave Speed 6.25 mm/sec, 12.5 mm/sec, 25 mm/sec, 50 mm/secAccuracy ± 1 bpm or 1%, whichever is greater (non-averaging)Beat-to -Beat (max.) MECG: 28 bpmDECG: 28 bpm (with Artifact Suppression On)Differential Input Impedance > 15MΩ
28 Specifications and Standards Compliance278WARNINGThe fetal/maternal monitor is not a diagnostic ECG device. In particular, the display of fetal/maternal ECG is intended only for evaluating signal quality for fetal/maternal heart rate as derived from the ECG waveform.When in doubt, it can be used to identify sources of compromised signal quality, such as noise or muscle artifacts. It can subsequently be used to verify the result of measures taken to resolve them (e.g., checking ECG cable connections or adapting the fetal ArtifactSuppress configuration).The safety and effectiveness of the displayed fetal/maternal ECG waveform (i.e., P, QRS and T segments) for evaluation of fetal/maternal cardiac status during labor have not been evaluated.Electrode Offset Potential Tolerance ± 400 mVFilter Bandwidth 0.8 to 80 HzINOP Auxiliary Current (Leads Off Detection) < 100 µAInput Signal Range DECG 20 µVpp to 6 mVppMECG 150 µVpp to 6 mVppDielectric Strength 1500 VrmsDefibrillator Protection NoneESU Protection NonePace pulse detection NonePerformance SpecificationsFetal Heart Rate (Ultrasound/DECG) Alarm Specifications FHR Alarm Limits Range Bradycardia(low limit)60 to 200 bpmadjustable in 10 bpm stepsDefault: 110 bpmTachycardia(high limit)70 to 210 bpmadjustable in 10 bpm stepsDefault: 170 bpmFHR Alarm Delay Range Bradycardia(low limit) Delay10 to 300 seconds in steps of 10sDefault: 240sTachycardia(high limit) Delay10 to 300 secondsin steps of 10sDefault: 300sSignal Loss Delay 10 to 30 secondsin steps of 10s
28 Specifications and Standards Compliance279Noninvasive Blood PressureComplies with IEC 80601-2-30:2010/EN 80601-2-30:2010.MECG Alarm Specifications Range AdjustmentMECG Alarm Limits High Range: 31 to 240Default: 120 bpm1 bpm steps (30 to 40 bpm)5 bpm steps (40 to 240 bpm)Low Range: 30 to 235Default: 50 bpmTachycardia Difference to high limit: 0 to 50 bpmDefault: 20 bpm5 bpm stepsClamping at: 150 to 240 bpmDefault: 200 bpm5 bpm stepsBradycardia Difference to low limit: 0 to 50 bpmDefault: 20 bpm5 bpm stepsClamping at: 30 to 100 bpmDefault: 40 bpm5 bpm stepsMaternal ECG Supplemental Information as required by IEC 60601-2-27Heart Rate Averaging Method The maternal heart rate is computed by averaging the 12 most recent RR intervals. If each of 3 consecutive RR intervals is greater than 1200 ms (i.e. rate less than 50 bpm), then the 4 most recent RR intervals are averaged to compute the HR.Display Update Rate 2 sResponse Time of Heart Rate Meter to Change in Heart RateHR change from 80 to 120 bpm: 10 sec.HR change from 80 to 40 bpm: 14 sec.Performance Specifications Measurement RangesSystolic 30 to 270 mmHg (4 to 36 kPa)Diastolic 10 to 245 mmHg (1.5 to 32 kPa)Mean 20 to 255 mmHg (2.5 to 34 kPa)Accuracy Max. Std. Deviation:8 mmHg (1.1 kPa)Max. Mean Error: ±5 mmHg (±0.7 kPa)Pulse Rate Range 40 to 300 bpmAccuracy(average over noninvasive blood pressure measurement cycle)40 to 100 bpm: ±5 bpm101 to 200 bpm: ±5% of reading201 to 300 bpm: ±10% of readingMeasurement Time Typical at HR > 60bpmAuto/manual: 30 seconds (adult)Maximum time: 180 seconds (adult)
28 Specifications and Standards Compliance280Measurement Validation: In adult mode, the blood pressure measurements determined with this device comply with the American National Standard for Electronic or Automated Sphygmomanometers (ANSI/AAMI SP10:2002/A1:2003) in relation to mean error and standard deviation, when compared to intra-arterial or auscultatory measurements (depending on the configuration) in a representative population. For the auscultatory reference the 5th Korotkoff sound was used to determine the diastolic pressure.SpO2Complies with EN/ISO 80601-2-61 2011 (except alarm system; alarm system complies with IEC 60601-1-8:2006).Measurement Validation: The SpO2 accuracy has been validated in human studies against arterial blood sample reference measured with a CO-oximeter. Pulse oximeter measurements are statistically distributed, only about two-thirds of the measurements can be expected to fall within the specified accuracy compared to CO-oximeter measurements.Cuff Inflation Time Typical for normal adult cuff: Less than 10 secondsInitial Cuff Inflation Pressure 165 ±15 mmHgAuto Mode Repetition Times 1, 2, 2.5, 3, 5, 10, 15, 20, 30, 45, 60 or 120 minutesVenipuncture Mode InflationInflation Pressure 20 to 120 mmHg (3 to 16 kPa)Automatic deflation after 170 secondsPerformance Specifications Alarm Specifications Range AdjustmentSystolic Adult: 30 to 270 mmHg (4 to 36 kPa) 10 to 30 mmHg: 2 mmHg (0.5 kPa)> 30 mmHg: 5 mmHg (1 kPa)Diastolic Adult: 10 to 245 mmHg (1.5 to 32 kPa)Mean Adult: 20 to 255 mmHg (2.5 to 34 kPa)Overpressure Settings Adjustment> 300 mmHg (40 kPa) > 2 sec not user adjustable
28 Specifications and Standards Compliance281Display Update Period: Typical: 2 seconds, Maximum: 30 seconds. Max. with noninvasive blood pressure INOP suppression on: 60 seconds.SpO2 Performance Specifications SpO2The specified accuracy is the root-mean-square (RMS) difference between the measured values and the reference valuesRange 0 to 100%Accuracy Philips Reusable Sensors:M1191A/B, M1191AL/BL, M1191ANL, M1192A, M1192AN = 2% (70% to 100%)M1191T, M1192T, M1194A, M1194AN, M1196A, M1196T = 3% (70% to 100%)Philips Disposable Sensors with M1943A(L):M1131A, M1901B, M1903B, M1904B = 3% (70% to 100%)M1133A, M1134A = ±2% (70% to 100%)NellcorPB® Sensors with M1943A(L):MAX-A, MAX-AL, MAX-P, MAX-N, D-25, D-20, N-25, OxiCliq A, P, N = 3% (70% to 100%)Masimo Reusable Sensors® with LNOP MP12 or LNC MP10:LNOP DC-I, LNOP DC-IP, LNOP YI, LNCS DC-I, LNCS DC-IP: 2% (70% to 100%)LNOP TC-I, LNCS TC-I: 3.5% (70% to 100%)Masimo Disposable Sensors® with LNOP MP12 or LNC MP10:LNOP Adt, LNOP Adtx, LNOP Pdt, LNOP Pdtx, LNCS Adtx, LNCS Pdtx: 2% (70% to 100%)LNOP Neo-L, LNCS Neo-L: 3% (70% to 100%)Resolution 1%Pulse Range 30 to 300 bpmAccuracy ±2% or 1 bpm, whichever is greaterResolution 1 bpmSensors Wavelength range 500 to 1000 nm.Information about the wavelength range can be especially useful to clinicians (for instance, when photodynamic therapy is performed).Emitted Light Energy≤ 15mWPulse Oximeter Calibration Range 70% - 100%SpO2 Alarm Specifications Range Adjustment DelaySpO250 to 100% 1% steps (0, 1, 2, 3,... 30) + 4 secondsDesat 50 to Low alarm limit 1% stepsPulse 30 to 300 bpm 1 bpm steps (30 to 40 bpm)5 bpm steps (40 to 300 bpm)max. 14 seconds
28 Specifications and Standards Compliance282Tympanic TemperatureComplies with:• EN 12470-5 (Clinical thermometers - Part 5:2003: Performance of infra-red thermometers)• ASTM E1965-98 (Infrared Thermometers for Intermittent Determination of Patient Temperature)with minor exceptions as noted below.Performance SpecificationsTachycardia Difference to high limit 0 to 50 bpm5 bpm steps max. 14 secondsClamping at 150 to 300 bpm 5 bpm stepsBradycardia Difference to low limit 0 to 50 bpm 5 bpm steps max. 14 secondsClamping at 30 to 100 bpm 5 bpm stepsSpO2 Alarm Specifications Range Adjustment DelayPerformance SpecificationsTemperature Resolution 0.1 °C or 0.1 °FResponse Time less than 2 secondsTemperature Calibrated Accuracy Specifications (out of the Factory)Ambient Temperature Target Temperature Accuracy25°C (77°F) 37.7°C to 38.9°C (98.4°F to 102°F) ±0.1°C (±0.2°F)16°C to 33°C (60.8° to 91.4°F)33°C to 42°C (91.4°F to 107.6°F) ±0.2°C (±0.4°F)Temperature Calibrated Accuracy Specifications (after recalibration using Genius 2 Checker/Calibrator)Ambient Temperature Target Temperature Accuracy16°C to 33°C (60.8° to 91.4°F)36°C to 39°C (96.8°F to 102.2°F) ±0.2°C (±0.4°F)16°C to 33°C (60.8° to 91.4°F)Less than 36°C or greater then 39°C (Less than 96.8°F or greater than 102.2°F)±0.3°C (±0.5°F)ASTM laboratory requirement for IR thermometers in the display range 37°C to 39°C (98°F to 102°F) is ±0.2°C (±0.4°F), whereas for mercury-in-glass and electronic thermometers, the requirement per ASTM standards E667-86 and E1112-86 is ±0.1°C (±0.2°F).Clinical accuracy characteristics and procedures are available from Covidien llc on request. To verify the accuracy, use a certified black body as specified in EN 12470-5:2003, Annex C, or use a Genius 2 Checker/Calibrator - available from Covidien llc under part number 303097.Clinical repeatability: meets section A.5 of EN 12470-5:2003 (E) per Covidien llc technical report. Data is available from Covidien llc on request.
28 Specifications and Standards Compliance283Physical SpecificationsDisplayed Temperature Measurement RangeMode Range °C Range °FEar 33.0 to 42.0 91.4 to 107.6Oral (ear + 0.6. °C) 33.6 to 42.0 92.5 to 107.6Core (ear + 1.04 °C) 34.0 to 42.0 93.2 to 107.6Rectal (ear + 1.16 °C) 34.2 to 42.0 93.6 to 107.6Caution: ASTM E1965-98 specifies 34.4°C to 42.2°C (94°F to 108°F)Ambient Temperature RangeMode Range °C Range °FOperating 10 to 95% RH, non-condensing16 to 33 60.8 to 91.4Storage up to 95% RH, non-condensing-25 to 55.0 -13 to 131Caution: EN12470-5 specifies 16.0°C to 35.0° C (60.8° F to 95° F), 10 to 95% RH, non-condensingASTM E1965-98 specifies 16.0°C to 40.0° C (60.8° F to 104° F), up to 95% RH, non-condensingStoring the thermometer outside the specified temperature/humidity range might adversely affect measurement accuracy. Check the calibration after storage in uncertain conditions.Tympanic Temperature Alarm SpecificationsRange 33.0°C to 42.0° C (91° F to 108° F)Adjustment 0.5° C steps (33° C to 35° C)0.1° C steps (35° C to 42° C)1.0° F steps (91° F to 95° F)0.2° F steps (95° F to 108° F)ThermometerDimensions 190 mm x 43 mm x 55 mm (±3 mm)Cable length 60 ±5 cm (spiral cable relaxed)250 ±15 cm (spiral cable extended)Weight (including cable) 180 ±10 gBase StationDimensions 205 mm x 65 mm x 75 mm (±3 mm)Weight (excluding cable) 400g ±10 mm
28 Specifications and Standards Compliance284Recorder SpecificationsBuilt-in Thermal Array Fetal Trace RecorderMechanism Thermal Array RecorderPaper & Printing Type Standard Z-fold paperStandard Speeds (real-time traces) 3 cm/min, 2 cm/min, 1cm/minFast Print Speed (stored traces) Max. 20 mm/sPrint speed is variable and depends on the print loadECG Wave Print Speed(not real-time)Emulated 25 mm/sPrint speed is variable and depends on the print loadPaper Advance 20 mm/sSensing Optical Reflex Sensor for black page marksAccuracy @ 3 cm/min, 2 cm/min,1 cm/min±5 mm/pageUsable Print Width 128 mmResolution 8 dots/mm (200 dpi)Time Delay to see trace on paper <30s @ 1 cm/minTrace Separation Offset for FHR (Ultrasound and DECG)Twin Standard FHR2 +20 bpmClassic FHR1 +20 bpmTriplet Standard FHR2 +20 bpmFHR3 -20 bpmClassic FHR1 +20 bpmFHR3 -20 bpmRecorder SymbolsSymbol DescriptionParameter is capable of alarming and alarms were enabled at the time of printing the annotation. Low / high limit are printed surrounding the symbol.Parameter is capable of alarming but alarms were disabled at the time of printing the annotation. (Note: There is no alarm related annotation at all if a parameter does not have alarming capability.)Alarm is on (printed next to measurement label)Upper and lower alarm limit (printed next to measurement label)
28 Specifications and Standards Compliance285FMP detection is onBeginning of the date/time annotationWarning (INOP)Measurement from a cableless transducer (printed next to measurement label)Measurement from a cableless maternal measurement Pod (SpO2 or NBP)Pulse from SpO2Pulse from Toco MPPulse from NBPTrace separation +20 bpm (in label)Trace separation -20 bpm (in label)Trace separation Off (in trace)Trace separation +20 bpm (in trace)Trace separation -20 bpm (in trace)Trace separation +20 bpm and -20 bpm (in trace)Recorder SymbolsSymbol Description
28 Specifications and Standards Compliance286Compatible External Displays: FM40/FM50 OnlyExternal displays can be connected with a maximum cable run of 10 m.* The video output of the Avalon FM40/FM50 has VGA resolution.Manufacturer's InformationYou can write to Philips at this address:Philips Medizin Systeme Boeblingen GmbHHewlett-Packard-Str. 271034 BoeblingenGermanyVisit our website for local contact information at: www.healthcare.philips.com© Copyright 2013. Koninklijke Philips N.V. All Rights Reserved.Trademark AcknowledgmentOxisensorTM II, Oxi-CliqTM, and OxiMaxTM are trademarks of Tyco Healthcare Group LP, Nellcor Puritan Bennett Division.Coincidence of heart rates is detectedMarkerSpecial wave, with different speed and scale (for example, fast printout of MECG wave on FM30)Recorder SymbolsSymbol DescriptionCompatible Display SpecificationsExternal XGA Display (M8031B)External SXGA Display (M8033C)Resolution* 1024 x 768 1280 x 1024 pixelRefresh frequency 60 Hz or 75 Hz 60 HzUseful screen Depends on size of displayPixel size
28 Specifications and Standards Compliance287Regulatory and Standards ComplianceThe monitor is in conformity with the requirements of the European Medical Devices Directive 93/42/EEC and bears the CE marking:The monitor is classified into Class IIb to Annex IX rule 10.Safety and PerformanceThe monitor complies with the following major international safety and performance standards:• IEC 60601-1:2005+A1:2012 / EN 60601-1:2006+AC:2010• IEC 60601-1-6:2010 / EN 60601-1-6:2010• IEC 60601-1-8:2006 / EN 60601-1-8:2007+AC:2010 • IEC 60601-2-27:2011+AC:2012 / EN 60601-2-27:2006+AC:2006 • IEC 80601-2-30:2009+C1:2010 / EN 80601-2-30:2010• IEC 60601-2-37:2007 / EN 60601-2-37:2008 • IEC 60601-2-49:2011 / EN 60601-2-49:2001• ISO 80601-2-61:2011 / EN 80601-2-61:2011 • ANSI/AAMI ES60601-1+C1:2009+A2:2010 • CAN/CSA C22.2#60601-1-08+TC2:2011 • JIS T 1303 2005• AS/NZS 3200.1.0-1998 The possibility of hazards arising from hardware and software errors was minimized in compliance with ISO 14971:2012, IEC 60601-1:2005+A1:2012 / EN 60601-1:2006+AC:2010.Alarm sounds are compliant with Standard ISO/IEC 9703-2 and IEC 60601-1-8:2006 / EN 60601-1-8:2007+AC:2010.
28 Specifications and Standards Compliance288Safety Tests Fetal MonitorAll the safety tests and procedures required after an installation or an exchange of system components are described in your monitor's Service Guide. These safety tests are derived from international standards but may not be sufficient to meet local requirements.WARNING• Do not use additional AC mains extension cords or multiple portable socket-outlets. If a multiple portable socket-outlet is used, the resulting system must be compliant with IEC/EN 60601-1 A1: 2012.• Do not connect any devices that are not supported as part of a system.• Do not use a device in the patient vicinity if it does not comply with IEC/EN 60601-1-1. The whole installation, including devices outside of the patient vicinity, must comply with IEC/EN 60601-1 A1: 2012. Any non-medical device, including a PC running an OB TraceVue/IntelliSpace Perinatal system, placed and operated in the patient's vicinity must be powered via a separating transformer (compliant with IEC/EN 60601-1 A1: 2012) that ensures mechanical fixing of the power cords and covering of any unused power outlets.• Do not use USB devices with own power supplies unless an appropriate separation device is used (either between USB interface and device or between device and power).During the installation the fetal monitor is configured for your environment. This configuration defines your custom default settings you work with when you switch on your fetal monitor. See the Fetal Monitor's Service Guide and the Configuration Guide for details on how to configure your fetal monitor.Electromagnetic Compatibility (EMC)The device and its accessories, listed in the accessories section, comply with the following EMC standards:• EN 60601-1-2+AC:2010 (IEC 60601-1-2:2007)Take special precautions regarding electromagnetic compatibility (EMC) when using medical electrical equipment. You must operate your monitoring equipment according to the EMC information provided in this book. Before using the device, assess the electromagnetic compatibility of the device with surrounding equipment.This ISM device complies with Canadian ICES-003:2012. Cet appareil ISM est conforme à la norme NMB-003 du Canada.CAUTION•FM20/FM30 only: Although this is an electrical Class II device, it has a protective earth conductor which is needed for EMC purposes.• Always use the supplied power cord with the three-prong plug to connect the monitor to AC mains. Never adapt the three-prong plug from the power supply to fit a two-slot outlet.
28 Specifications and Standards Compliance289CAUTIONThe use of accessories, transducers and cables other than those specified may result in increased electromagnetic emissions or decreased electromagnetic immunity of the device.WARNINGDo not use cordless/mobile phones or any other portable RF communication system within the patient vicinity, or within a 1.0 m radius of any part of the fetal monitoring system.WARNINGFor paced patients: The radiated SRR power of the CL SpO2 and CL NBP Maternal Cableless Measurement Devices, and other sources of radio-frequency energy, when used in very close proximity of a pacemaker, might be sufficient to interfere with pacemaker performance. Due to shielding effects of the body, internal pacemakers are somewhat less vulnerable than external pacemakers. However, caution should be exercised when monitoring paced patients.In order to minimize the possibility of interference, avoid positioning and wearing the Cableless Measurement Devices in very close proximity to a pacemaker. Consult the pacemaker manufacturer for information on the RF susceptibility of their productsEMC TestingCAUTIONFetal parameters, especially ultrasound and ECG, are sensitive measurements involving small signals, and the monitoring equipment contains very sensitive high gain front-end amplifiers. Immunity levels for radiated RF electromagnetic fields and conducted disturbances induced by RF fields are subject to technological limitations. To ensure that external electromagnetic fields do not cause erroneous measurements, it is recommended to avoid the use of electrically radiating equipment in close proximity to these measurements.
28 Specifications and Standards Compliance290Reducing Electromagnetic InterferenceCAUTIONThe device should not be used adjacent to, or stacked with, other equipment unless otherwise specified.The product and associated accessories can be susceptible to interference from continuous, repetitive, power line bursts, and other RF energy sources, even if the other equipment is compliant with EN 60601-1-2 emission requirements. Examples of other sources of RF interference are other medical electrical devices, cellular products, information technology equipment, and radio/television transmissions.When electromagnetic interference (EMI) is encountered, for example, if you can hear spurious noises on the fetal monitor's loudspeaker, attempt to locate the source. Assess the following:• Is the interference due to misplaced or poorly applied transducers? If so, re-apply transducers correctly according to directions in this book or in the Instructions for Use accompanying the accessory.• Is the interference intermittent or constant?• Does the interference occur only in certain locations?• Does the interference occur only when in close proximity to certain medical electrical equipment?Once the source is located, there are a number of things that can be done to mitigate the problem:1Eliminating the source. Turn off or move possible sources of EMI to reduce their strength.2Attenuating the coupling. If the coupling path is through the patient leads, the interference may be reduced by moving and/or rearranging the leads. If the coupling is through the power cord, connecting the system to a different circuit may help.3Adding external attenuators. If EMI becomes an unusually difficult problem, external devices such as an isolation transformer or a transient suppressor may be of help. Your service provider can be of help in determining the need for external devices.Where it has been established that electromagnetic interference is affecting physiological parameter measurement values, a physician, or a suitably qualified person authorized by a physician, should determine if it will negatively impact patient diagnosis or treatment.System CharacteristicsThe phenomena discussed above are not unique to this system but are characteristic of fetal patient monitoring equipment in use today. This performance is due to very sensitive high gain front end amplifiers required to process the small physiological signals from the patient. Among the various monitoring systems already in clinical use, interference from electromagnetic sources is rarely a problem.
28 Specifications and Standards Compliance291Electromagnetic Emissions and ImmunityThe EMC standards state that manufacturers of patient-coupled equipment must specify immunity levels for their systems. See Tables 1 to 4 for this detailed immunity information. See Table 5 for recommended minimum separation distances between portable and mobile communications equipment and the product.Immunity is defined in the standard as the ability of a system to perform without degradation in the presence of an electromagnetic disturbance.Caution should be exercised in comparing immunity levels between different devices. The criteria used for degradation are not always specified by the standard and can therefore vary with the manufacturer.In the table below, the term "device" refers to the Avalon FM20/30/40/50 fetal monitor together with its accessories. The table gives details of the electromagnetic emissions, and how these are classified, for the device, and the electromagnetic environments in which the device is specified to technically function.1 Note that the device is not intended for home use.Electromagnetic ImmunityThe monitor is suitable for use in the specified electromagnetic environment. The user must ensure that it is used in the appropriate environment as described below.Table 1 - Guidance and Manufacturer's Declaration: Electromagnetic EmissionsEmissions Test Compliance Avoiding Electromagnetic InterferenceRadiofrequency (RF) emissions Group 1 The device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.Harmonic emissions IEC 61000-3-2 Class AVoltage fluctuations and flicker IEC 61000-3-3 compliesRF emissions CISPR 11For the Avalon FM20/30 fetal monitor with all accessories except the IUP/ECG patient module M2738A.Class B The device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage supply network that supplies buildings used for domestic purposes 1.RF emissions CISPR 11For the Avalon FM40/FM50 with all accessories.For the Avalon FM20/30 fetal monitor whenever used with the IUP/ECG patient module M2738A.For the Avalon CTS Interface Cable (M2731-60001/M2732-60001) whenever used with the Avalon CTS Cableless Fetal Transducer System.For the Avalon CL Base Station with cableless transducers whenever used with the fetal monitors.Class A The device is suitable for use in all establishments other than domestic establishments and those directly connected to the public low-voltage supply network that supplies buildings used for domestic purposes.
28 Specifications and Standards Compliance292Table 2 - Guidance and Manufacturer's Declaration: Electromagnetic ImmunityImmunity Test IEC 60601-1-2 Test LevelCompliance Level Electromagnetic Environment GuidanceElectrostatic discharge (ESD) IEC 61000-4-2± 6 kV contact± 8kV air± 6 kV contact± 8kV airFloors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.Electrical fast transient/burstIEC 61000-4-4± 2 kV for power supply lines± 1 kV for input/output lines± 2 kV for power supply lines± 1 kV for input/output linesMains power quality should be that of a typical commercial and/or hospital environmentSurge IEC 61000-4-5± 1 kV differential mode± 2 kV common mode± 1 kV differential mode± 2 kV common modeMains power quality should be that of a typical commercial and/or hospital environmentVoltage dips, short interruptions and voltage variations on power supply input linesIEC 61000-4-11<5% UT (> 95% dip in UT) for 0.5 cycles<5% UT (> 95% dip in UT) for 0.5 cyclesMains power quality should be that of a typical commercial and/or hospital environment. If the user of the device requires continued operation during power mains interruptions, it is recommended that the device is powered from an uninterruptible power supply.40% UT (60% dip in UT) for 5 cycles40% UT (60% dip in UT) for 5 cycles70% UT(30% dip in UT) for 25 cycles70% UT (30% dip in UT) for 25 cycles< 5% UT(> 95% dip in UT) for 5 sec< 5%UT (> 95% dip in UT) for 5 secPower frequency (50/60 Hz) magnetic fieldIEC 61000-4-83 A/m 3 A/m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial and/or hospital environmentKey: UT is the AC mains voltage prior to application of the test level.
28 Specifications and Standards Compliance293Radio Compliance NoticeAvalon CL with WMTSOperation of this equipment requires the prior coordination with a frequency coordinator designated by the FCC for the Wireless Medical Telemetry Service.This device complies with Part 15 of the FCC Rules and RSS-210 of Industry Canada. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Any changes or modifications to this equipment not expressly approved by Philips Medical Systems may cause harmful radio frequency interference and void your authority to operate this equipment.Installation of this telemetry device is permitted in hospitals and health care facilities only. This device shall not be operated in mobile vehicles (including ambulances and other vehicles associated with health care facilities). The installer/user of this device shall ensure that it is at least 80 km from the Dominion Radio Astrophysical Observatory (DRAO) near Penticton, British Columbia. The coordinates of DRAO are: latitude N 49E 19' 15", longitude W 119° 37′ 12″. For medical telemetry systems not meeting this 80 km separation (e.g. the Okanagan Valley, British Columbia) the installer/user must coordinate with, and obtain the written concurrence of, the Director of DRAO before the equipment can be installed or operated. The Director of DRAO may be contacted at 250-497-2300 (telephone) or 250-497-2355 (fax). (Alternatively, the Manager, Regulatory Standards, Industry Canada, may be contacted.)Le présent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils radio exempts de licence. L'exploitation est autorisée aux deux conditions suivantes: (1) l'appareil ne doit pas produire de brouillage, et (2) l'utilisateur de l'appareil doit accepter tout brouillage radioélectrique subi, même si le brouillage est susceptible d'en compromettre le fonctionnement.L'utilisation de cet appareil de télémesure est permise seulement dans les hôpitaux et établissements de soins de santé. Cet appareil ne doit pas être mis en marche dans des véhicules (y compris les ambulances et autres véhicules associés aux établissements de santé). La personne qui installe/utilise cet appareil doit s’assurer qu’il se trouve à au moins 80 km de l’Observatoire fédéral de radioastrophysique (OFR) de Penticton en Colombie-Britannique. Les coordonnées de l’OFR sont : latitude N 49° 19’ 15», longitude O 119° 37 12 ′′. La personne qui installe/utilise un système de télémesure médicale ne pouvant respecter cette distance de 80 km (p. ex. dans la vallée de l’Okanagan (Colombie-Britannique), doit se concerter avec le directeur de l’OFR et obtenir de sa part une autorisation écrite avant que l’équipement ne puisse être installé ou mis en marche. Le directeur de l’ OFR peut être contacté au 250-497-2300 (tél.) ou au 250-497-2355 (télécopieur). (Le Directeur des Norm es réglementaires d’Industrie Canada peut également être contacté).Avalon CL with T108Japanese Radio Law and Japanese Telecommunications Business Law Compliance. This device should not be modified (otherwise the granted designation number will become invalid).
28 Specifications and Standards Compliance294Finding Recommended Separation DistancesIn the following table, P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer, and d is the recommended separation distance in meters (m).Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance calculated from the equation appropriate for the frequency of the transmitter.Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, should be less than the compliance level in each frequency range.Interference may occur in the vicinity of equipment marked with this symbol:Table 3 - Guidance and Manufacturer's Declaration: Electromagnetic ImmunityConducted RF Immunity Test EN/IEC 61000-4-6IEC 60601-1-2 Test Level over 150 kHz to 80 MHz Compliance LevelElectromagnetic Environment Guidance:Recommended Separation Distance (d)(in Meters, at Frequency Range Tested)for Ultrasound and ECG Measurements3.0 VRMS 3.0 VRMS d = 1, 2√PKey: d = Recommended separation distance in meters (m)P = maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturerV1 = Tested compliance level (in Volts) for the Conducted RF Immunity test IEC 61000-4-6The device meets the compliance level of 3.0 VRMS according to IEC 60601-1-2 over the specified test frequency range. Over the frequency range 150 kHz to 80 MHz, the recommended separation distance in meters (d) is found by the following equation:For a compliance level of 3.0 VRMS:d = 1, 2√PTable 4 - Guidance and Manufacturer's Declaration: Electromagnetic ImmunityRadiated RF Immunity Test EN/IEC 61000-4-3IEC 60601-1-2 Test Level over 80 MHz to 2.5 GHz Compliance LevelElectromagnetic Environment Guidance:Recommended Separation Distance (d)(in Meters, at Frequency Range Tested)for Ultrasound and ECG Measurements3.0 V/m 3.0 V/m Over 80 MHz to 800 MHz:d = 1, 2√POver 800 MHz to 2.5 GHz:d = 2, 3√P
28 Specifications and Standards Compliance295Field strengths from fixed transmitters, such as base stations or radio (cellular, cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the device is used exceeds the applicable RF compliance level above, it should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the device.These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.If you require further information or assistance, please contact Philips Support.Key: d = Recommended separation distance in meters (m)P = maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturerE1 = Tested compliance level (in Volts/meter) for the Radiated RF Immunity test IEC 61000-4-3The device meets the compliance level of 3.0 VRMS according to IEC 60601-1-2 over the specified test frequency range.Over the frequency range 80 kHz to 800 MHz, the recommended separation distance in meters (d) is found by the following equation:For a compliance level of 3.0 VRMS:d = 1, 2√POver the frequency range 800 kHz to 2.5 GHz, the recommended separation distance in meters (d) is found by the following equation:For a compliance level of 3.0 VRMS:d = 2, 3√PTable 4 - Guidance and Manufacturer's Declaration: Electromagnetic ImmunityRadiated RF Immunity Test EN/IEC 61000-4-3IEC 60601-1-2 Test Level over 80 MHz to 2.5 GHz Compliance LevelElectromagnetic Environment Guidance:Recommended Separation Distance (d)(in Meters, at Frequency Range Tested)for Ultrasound and ECG Measurements
28 Specifications and Standards Compliance296Recommended Separation Distances from Other RF EquipmentThe device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment and the device as recommended below, according to the maximum output power of the communications equipment.Radio Frequency Radiation Exposure InformationThe radiated output power of the device is far below the FCC radio frequency exposure limits. Nevertheless, the device shall be used in such a manner that the potential for human contact during normal operation is minimized.EnvironmentBefore operation, make sure that the fetal monitor is free from condensation. This can form when equipment is moved from one building to another, and is exposed to moisture and differences in temperature.Use the monitor in an environment which is reasonably free from vibration, dust, corrosive or explosive gasses, extremes of temperature, humidity, and so forth. It operates within specifications at ambient temperatures between 0 and +45°C (32°F to 113°F). Ambient temperatures that exceed these limits can affect the accuracy of the system, and can damage the components and circuits.Ambient temperature ranges for storage are -20°C to +60°C (-4°F to 140°F) for the monitor, and -40°C to +60°C (-40°F to 140°F) for transducers.The transducers are watertight to a depth of 1.0 m for at least five hours (rated IP 68).WARNING•Leakage currents: If several items of equipment used to monitor a patient are interconnected, the resulting leakage current may exceed allowable limits.•ECG electrodes: NEVER allow ECG electrodes to contact other electrical conductive parts, including earth.Table 5 - Separation Distance (d) in Meters According to Frequency of Transmitter at IEC 60601-1-2 Test Compliance LevelRated Maximum Output Power (P) of Transmitter (in Watts)150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz0.01 W 0.1 m 0.1 m 0.23 m0.1 W 0.4 m 0.4 m 0.7 m1 W 1.2 m 1.2 m 2.3 m10 W 3.8 m 3.8 m 7.3 m100 W 12.0 m 12.0 m 23.0 m
28 Specifications and Standards Compliance297Monitoring After a Loss of PowerIf the monitor is without power for less than one minute, monitoring will resume with all active settings unchanged. If the monitor is without power for more than one minute, the behavior depends on your configuration. If Automat. Default is set to Yes, the User Defaults will be loaded when power is restored. If Automat. Default is set to No, all active settings are retained, if power is restored within 48 hours. The Automat. Default setting is made in Configuration mode.FM20/30withBatteryOption,FM40/50When power is lost - no power is available from the AC power source or from the battery - a beeper will sound. The tone can be silenced by pressing the On/Standby switch.ESU, MRI and DefibrillationWARNINGThe fetal/maternal monitors are NOT intended for use during defibrillation, electro-surgery, or MRI. Remove all transducers, sensors, and accessories before performing electro-surgery, defibrillation, or MRI, otherwise harm to the patient or the user can result.Cardiac Pacemakers and Electrical StimulatorsWARNINGThe fetal/maternal monitors are not intended for use for ECG measurements on patients connected to external electrical stimulator or with cardiac pacemakers.Fast Transients/BurstsThe equipment will return to the previous operating mode within 10 seconds without loss of any stored data.
28 Specifications and Standards Compliance298Symbols on the SystemThis caution/warning symbol indicates that you should consult the Instructions for Use (this document), and particularly any warning messages.Connection direction indicatorFM20/FM30 with battery optionThis symbol indicates that you should consult the Instructions for Use (this document).Mouse connection indicator(optional)Power-On/Off Switch - FM20/FM30 without Battery OptionKeyboard connection indicator(optional)Power-On/StandBy Switch - FM40/FM50 and FM20/30 with Battery OptionSerial/MIB connector(optional)Power-On LED USB interface(optional)Electrical Class II equipment, in which the protection against electric shock relies on double or reinforced insulation (FM20/FM30).VideoAnalog interface indicator for connection to any analog video display (VGA resolution) FM40/FM50 Fetal Sensor Socket symbol. IP 67 Ingress Protection code according to IEC 60529. The IUP/ECG patient module (M2738A) is rated IP 67 (protection against dust, access to hazardous parts, and the effects of continuous immersion in water to a depth of 0.5 meter for 30 minutes).
28299SpO2 Socket symbol. IP 68 Ingress Protection code according to IEC 60529. All transducers (excluding M2738A) are rated IP 68 (protection against dust, access to hazardous parts, and the effects of continuous immersion in water to a depth of 1.0 meter for five hours).Noninvasive Blood Pressure Socket symbol.IP X1 Ingress Protection code according to IEC 60529. The monitors and interface cable for the Avalon CTS (M2731-60001/M2732-60001) are rated IP X1 (protection against water dripping vertically only).Symbol indicating the monitor has the triplets option.Type CF equipment, not defibrillation proof.Symbol indicating the monitor is capable of intrapartum monitoring.Indicates location of service numberButton to open paper drawer/paper eject. (FM40/FM50).Indicates location of serial numberProtective earth terminal (FM40/FM50).Indicates location of catalog numberEquipotential grounding point (FM40/FM50).Indicates location of the date of manufacture and/or name and address of manufacturer
28 Specifications and Standards Compliance300Socket for connecting Avalon CTS interface cable M2732-60001 or Avalon CL interface cable (with black connector, FM40/FM50)Identifies the year and month of manufacture.Symbol indication for non-ionizing radiation. Symbol indicating separate collection for waste electrical and electronic equipment.China ROHS CSA US mark GOST-R mark R&TTE Compliance Association: "Class 2 Device" Mark FCC ID Federal Communications Commission: FCC ID xxxxCMIIT ID Chinese Radio marking: CMIIT ID (China Ministry of Industry and Information Technology) Japanese Radio marking: Radio mark + "PMS Japan" (in Japanese) + Prod. No. + [R]-symbol + ID "Taiwan Radio Label" (NCC Logo) + ID Korea radio mark: KC logo, KCC ID number, and Conformity assessment informationIndustrial, Scientific, & Medical radio frequency band (Avalon CL frequency band used e.g. in the EU)Wireless Medical Telemetry Service (Avalon CL frequency band used e.g. in North America)Association Of Radio Industries And Businesses T108 (Avalon CL frequency band used e.g. in Japan)CE marking accompanied by the VDE NB number 0366IC-ID (Industry Canada ID)One IC-ID labeling for each built in radio: OBR, SRR Taiwan Radio Label (NCC Logo) + ID
29 Default Settings Appendix30129Default Settings AppendixThis appendix documents the most important default settings of your fetal monitor and the Avalon CL Base Station with the cableless transducers as they are delivered from the factory. For a comprehensive list and explanation of default settings see the Configuration Guide supplied with your fetal monitor. The monitor's default settings can be permanently changed in Configuration Mode.Alarm and Measurement Default SettingsAlarm Defaults SettingsAlarm Setting Choice DefaultAlarm Mode INOP only, All INOP onlyAlarm Volume 0..10 5Alarms Off 1 min, 2 min, 3 min, Infinite 3 minAlarm Text Standard/Enhanced StandardVisual Latching Red&Yellow/Red/Off OffAudible Latching Red Only/Off OffAlarm Sounds Traditional/ISO TraditionalAlarm Low 0..10 4Fetal / Maternal Defaults SettingsFHR (Ultrasound/DECG) Alarms On/Off Default OnDefault Color for FHR Numeric OrangeToco Default color for Toco numeric GreenIUP Default IUP Scale Unit mmHgDefault color for IUP numeric GreenMaternal Heart Rate HR MeasurementDefault Color for MECG Numeric Red
29 Default Settings Appendix302Coincidence Default SettingsNBP Default SettingsCL NBP Default SettingsCoincidence Default SettingsCoincidence Tone immediatelyFactory Default Settings Mode ManualRepeat Time 15 minAlarms from Sys.Low Limit 90 / 50 (60)High Limit 160 / 90 (110)VP Pressure mmHgDone Tone OffVeni Puncture 60 mmHgStart Time SynchronizedNBP OnAlarms OnColor RedReference AuscultatoryNBP Setting Factory DefaultsMode AutoRepeat Time 10 minNBP OnVP Pressure 60 mmHgReference AuscultatoryUnit mmHgDone Tone OffStart Time SynchronizedAging Time 10 minColor Red
29 Default Settings Appendix303SpO2 Default SettingsCL SpO2 Default SettingsSpO2 Factory Default SettingsDesat Limit 80Low Limit 90Low Limit 100High Limit 20 secondsDesat Delay 10 secondsLow Alarm Delay 10 secondsHigh Alarm Delay 10 secondsNBP Alarm Suppr. OnAlarms OnColor CyanPulse Default SettingsPulse (SpO₂)OnHigh Limit 120 bpmLow Limit 50 bpmBradycardia: Difference to Low Limit20 bpmBradycardia: Clamp 40 bpmTachycardia: Difference to High Limit20 bpmTachycardia: Clamp 200 bpmSpO2 Settings Factory DefaultsRepeat Time 15 minSignal Quality OnNBP Alarm Suppr. OnColor
29 Default Settings Appendix304Tympanic Temperature Default SettingsManually Entered Values Default SettingsRecorder Default SettingspTemp Settings Factory defaults H10/H20/H40 H30 (deviations from H10/H20/H40)Adult AdultLow Limit 36°C (96.8°F)High Limit 39°C (102.2°F)Unit °CAlarms OnColor GreenManual Entered Values Default SettingsLabel TempUnit ºCColor whiteInterval 1hMsmt offSetting Choice DefaultRecorder Speed 1, 2, or 3 cm/min 3 cm/minScale Type US, Internat'l USTrace Style FHR1 Thin, Medium, Thick, Extra Thick ThickTrace Style FHR2 MediumTrace Style FHR3 Extra ThickTrace Style Toco ThickTrace Style HR ThinWave Style ECG ThinECG Wave printing choice Separate, Overlap SeparateNotes Recording Along, Across AlongAuto Start Off, On OffConfirmed Stop OffBridge Paperout OnPaper Save Mode OffNST Autostart OnNST Autostop OffTrace Separation OffSeparation Order Standard, Classic Standard
29 Default Settings Appendix305Intensity 4 (medium) n/aCal. Offset 5 n/aSetting Choice Default
29 Default Settings Appendix306
3171IndexAaccessories 267, 268, 270, 271, 272, 273, 277cl NBP pod accessories 272cl SpO2 pod accessories 276fetal accessories 268fetal recorder accessories 277latex information 267MECG accessories 270noninvasive blood pressure accessories 270, 271, 272adult cuffs 272multi-patient comfort cuff kits 271reusable cuffs 271single-hose disposable cuffs 272SpO2 accessories 273Philips sensors (disposable) 273Philips sensors (reusable) 273transducer accessories 268ACOG technical bulletin 80actions after monitoring 98active alarms 109adjusting brightness 66adjusting display 68adjusting screen brightness 66admitting a patient 137, 138editing information 138aging numerics 213alarms 109, 110, 111, 113, 114, 115, 116, 117, 118, 120, 121, 123, 191, 216, 230, 285, 289, 290, 311acknowledging alarms 114active alarms 109alarm behavior at on/off 121alarm latching 119alarm limit delay 285alarm reminder 114alarm standards 111audible alarm indicators 111yellow alarms 109artifact suppression 208artifact suppression and fetal arrhythmia 208explanation of artifact suppression 208switching on and off artifact suppression 208automatic noninvasive blood pressure repeat time 215Bbaseline measurement 177, 184, 194Battery Option 101using batteries 101belt actions 70, 72belt fastening 70belt fixing button 70CCableless Monitoring 91Avalon CL 40configuration cableless system 92important considerations 159LED indication 53TELE window 93Telemetry 94Underwater monitoring 97calibration 216, 260calibrating noninvasive blood pressure 260cautions 9changing FHR alarm delays 191changing FHR alarm limits 191cleaning monitor actions 255, 256, 257, 265cleaning method 256cleaning monitoring accessories 257general cleaning requirements 255infection control 255printhead cleaning 265configuration mode 63configuring alarm tone 111confirming fetal life 10, 158, 175, 183connecting power 12cross-channel verification 10, 175, 183, 234CCV and triplets 183CCV and twins 175Ddata recovery 251date from OB TraceVue 66date setting 66DECG 205, 209, 285DECG INOPs 209DECG specifications 285DECG testing 209DECG troubleshooting 209default alarm settings 311default IUP settings 285default settings 285FHR default settings 285IUP default settings 285MECG default settings 285Toco default settings 285user defaults 65defibrillation precautions 238, 267, 307demo mode 63disabling touchscreen 63discharging a patient 138disinfecting 255, 256, 257infection control 255recommended substances 257display 68, 213, 285adjusting display 68display noninvasive blood pressure 213fetal display specifications 285disposal of electronic waste 266disposal of monitor 266dyshemoglobins 228intravascular dyshemoglobins 228Eearly systolic blood pressure 213ECG 205, 235, 285ECG specifications 285electrical safety tests 298electrical surgery precautions. See ESU 228, 238, 267, 307electrodes 237applying electrodes 237EMC 298electromagnetic compatibility 298electromagnetic emissions 301electromagnetic interference 300how to reduce electromagnetic interference 300EMC and compliant accessories 298EMC precautions 298EMC standards 298entering notes 61ESU precautions 238, 267, 307event marker remote 80extension cable for SpO2 228external monitoring 157, 176, 184, 194external monitoring - Toco 194external monitoring - triplets 184external monitoring - twins 176external monitoring - ultrasound 157
318Ffactory defaults 289, 290, 294noninvasive blood pressure factory defaults 289recorder factory defaults 294SpO2 factory defaults 290FAST 227Fourier Artifact Suppression Technology 227fetal accessories 268fetal arrhythmia 208fetal demise 10fetal display specifications 285IUP - fetal display specifications 285Toco - fetal display specifications 285US - fetal display specifications 285fetal heart rate alerting. See FHR 191fetal heart rate. See FHR 157fetal movement 163fetal movement profile. See FMP 157FHR 10, 158, 165, 175, 177, 183, 184, 191, 192, 234, 285alerting 191cross-channel verification 234misidentification 10trace separation 177, 184FHR alarms 285finder LED 45, 73, 175, 183finding monitor revision 67flexible nurse call 30, 42, 44FMP 163, 164FMP and twins 163FMP statistics 163functional arterial oxygen saturation 227Gglobal settings 65Hhigh priority alarms 109Iinfection control 255infection and sterilizing 255INOPs 109, 114CCV INOP 33coincidence tone 30disconnect INOPs 114INOP alarms 109INOPs indicators 109silencing INOPs 114interference 298, 300how to reduce interference 300interference from RF equipment 298internal monitoring 177, 199, 201intrauterine pressure. See IUP 197intravascular dyshemoglobins 228intravascular dyshemoglobins effects on (SpO2) 228ISO/IEC standard 9703-2 111IUP 197, 199, 285IUP specifications 285Llatching alarms 118, 119latching alarm behavior 119Mmains power (AC) 12, 99connecting to mains power 12disconnecting from mains power 99maintenance 259, 260maintenance schedule 259, 260visual inspection 259maternal ECG 208, 238, 240electrode position 238printing waveform 208, 240viewing waveforms 238maternal heart rate 233, 234, 235maternal heart rate and cross-channel verification 234maternal heart rate and priorities 233maternal heart rate from MECG 235sources of maternal heart rate 233maternal puls from Toco 32Maternal Temperature 30measurement settings 65changing measurement settings 65entering setup menu 65measurements 64, 65, 285setting up measurements 65switching on and off measurements 64MECG 208, 235, 237, 238, 240, 242, 243, 270, 285accessories 270alarm limits 285connection illustration 235default settings 285electrodes 237specifications 285waveform printing 208, 240MECG alarm limits 285methemoglobin (SpO2) 228MHR 158, 233, 235, 237MHR from MECG 235MHR priorities 233MHR sources 233monitor settings 10, 40, 66, 68, 98, 251changing monitor settings 66major parts and keys 40power on/off behavior 99Standby 98switching on 68monitoring mode 63monitoring triplets and FHR 183monitoring twins and FHR 175MR imaging and the SpO2 transducer 228MRI precautions 238, 267, 307NNBP. See noninvasive blood pressure 211NIBP. See noninvasive blood pressure 211Noninvasive Blood Pressure (NBP) 211, 212, 213, 214, 215, 216, 217, 242, 260, 270, 271, 272, 289calibration interval 260comfort cuff kits 271factory defaults 289how the measurement works 211measurement 212, 214limitations 212methods 212starting 214stopping 214NBP accessories 270NBP adult cuffs 272NBP automatic mode 215NBP numerics 213NBP pediatric cuffs 272NBP performance specifications 289NBP reusable cuffs 271NBP single-hose disposable cuffs 272NBP site inspection 212NBP troubleshooting 217NBP venous puncture 216preparing to measure NBP 212non-medical devices 298non-medical devices in patient vicinity 298Non-Stress Test timer. See NST timer 143NST ReportNST analysis 32Trace Interpretation 145, 148NST timer 141, 142, 143OOB TraceVue 38, 39, 252connection to OB TraceVue 38, 39LAN connection 252operating modes 63configuration mode 63demo mode 63monitoring mode 63service mode 63operating temperatures 306
319oscillometric measurement method 211PPaging Patient 97paper 80, 81, 82, 83, 85, 264, 277default paper speed 80loading paper 83, 85paper out INOP 82paper speed 80changing 80default 80defaults 80setting 80paper, when to reload 82recorder paper 277removing paper 83, 85storing paper 264tearing off a trace 81Paper Advance key 61Paper-Out indication 82passcode protection 63patient alarms 123Patient Demographics window 137patient module 205, 235paused alarms 115, 116restarting paused alarms 116pausing alarms 115performance specifications 285, 289, 290noninvasive blood pressure specifications 289SpO2 specifications 290physiological alarms 109pop-up keys 95power 12, 99connecting power 12disconnecting from 99power connection 12power failure 99pulse 242pulse from noninvasive blood pressure 242pulse rate 233Rrecorder 76, 100, 264, 265, 277, 294factory defaults 294paper storage 264printhead cleaning 265recorder paper 277recorder specifications 294recorder speed 33recorder troubleshooting 100Recorder Elements 79recording stored data 61recovering traces 251trace recovery printout 251recycling 266red alarms 109regulatory compliance 297remote event marker 80restarting paused alarms 116reviewing alarms 118reviewing alarms window 118Ssafety 260, 297maintenance interval 260safety standards 297screen layouts 64selftest 68, 76, 120sensor 227disposable SpO2 sensors 227selecting SpO2 sensors 227separating FHR traces 177, 184separating triplet traces 184separating twin traces 177service mode 63settings 64, 65, 66active settings 64changing settings 66global settings 65monitor settings 66user default settings 65signal loss delay 192signal quality 90, 230signal quality during monitoring 90signal quality of SpO2 230silencing alarms 114specifications 279, 281, 285, 294built-in recorder specifications 294DECG specifications 285ECG specifications 285environmental specifications 279monitor 279SpO2 sensors 279transducers 279IUP specifications 285measurement specifications 285MECG specifications 285performance specifications 285Toco specifications 285transducer specifications 281US specifications 285SpO2 227, 228, 230, 273, 290accessories 273alarm specifications 290connecting the cables 228disposable sensors 227factory defaults 290FAST technology 227performance specifications 290Philips sensors (disposable) 273Philips sensors (reusable) 273signal quality 230SpO2 alarms 230, 290standards 297, 298EMC standards 298safety standards 297standards compliance 297Standby 61sterilizing 255, 258infection control 255storage temperatures 306stored data recording 61suppressing artifacts 208suspended alarm 116suspicious SpO2 reading 230switching on and off 164switching on and off alarms 116switching on monitor 68switching on recorder 76symbols on the system 308Ttechnical alarm messages. See INOPs 126temperatures 306operating temperatures 306storage temperatures 306testing 120, 209, 242, 298DECG testing 209MECG testing 242safety testing 298testing alarms 120time 66setting time 66time from OB TraceVue 66Toco 193, 194, 195, 205, 237, 285default Toco settings 285testing a Toco transducer 195Toco baseline 194Toco display specifications 285Toco monitoring 193Toco sensitivity 195Toco specifications 285Toco MP transducer 193, 233Toco+ transducer 193touch tone volume 66touchscreen operation 56, 63trace actions 81, 251, 252separation on/off 33tearing off traces 81trace recovery on OB TraceVue 252trace recovery on paper 251transducer 45, 70, 73, 173, 175, 183, 193, 195,
320281connecting transducer to monitor 73fixing transducer to belt 70repositioning transducers 73Toco transducer 193Toco+ transducer 193transducer belt clip 70transducer specifications 281transducer testing 173, 195Toco 195ultrasound 173triplets 183, 184, 185, 188cross-channel verification 183external monitoring 184importance of monitoring MHR 183monitoring triplets 183offsetting baselines 184troubleshooting 100, 165, 181, 188, 195, 199, 209, 217, 240DECG 209FHR 165IUP 199MECG 240troubleshooting FHR 165twins 163, 175, 176, 177, 178, 179, 181cross-channel verification 175external monitoring 176importance of monitoring MHR 175invasive monitoring 177monitoring FHR 175monitoring twins 175offsetting baselines 177twins and FMP 163Uultrasound 157, 160, 173, 285applying gel 160testing a transducer 173ultrasound display specifications 285ultrasound monitoring 157ultrasound specifications 285understanding screens 64USB 30using the adapter cable 205uterine activity 193, 194, 195, 197, 199, 205, 237external monitoring 193internal monitoring 197monitoring uterine activity 194, 197, 199, 205, 237troubleshooting uterine activity 195, 199Vvelcro belt 72venous puncture 216visual alarm indicators 110voltage setting 12volume 66, 113alarm volume 113IUP, zeroing 199touch tone volume 66warnings 9
Part Number xxxxxxxxxxxPrinted in Germany 06/13*453564405521*

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