Spacelabs Healthcare 76A91343-1400 91343-09/91347-09 User Manual 2 of 3
Spacelabs Healthcare, Inc. 91343-09/91347-09 Users Manual 2 of 3
Contents
- 1. Users Manual 1 of 3
- 2. Users Manual 2 of 3
- 3. Users Manual 3 of 3
Users Manual 2 of 3
To Initiate ECG monitoring: Select a transmitter. Note its channel number. Attach lead wires to transmitter. Attach lead wires to electrodes. Apply electrodes to patient. Install a transmitter battery. Close the transmitter case “manure-A ECG Contents Overview ............... Setting Up ECG Monitoring . Display Detail ........... Monitoring Faced ECG Patients . Restoring Delault Settings. . Changing the Display Resolution. Selecting Options lor Lead Display . . ECG Alarm Message summary ........................ wflmmmb—A-n Overview Digital telemetry ECG monitoring provides continuous monitoring ot electrocardiographic signals in order to detect abnormal cardiac rhythms, including life-threatening arrhythmias such as asystole, ventricular fibrillation, and ventricular tachycardia. Setting Up ECG Monitoring To set up ECG monitoring, plug each lead wrre into the transmitter, connect each to an electrode, and then attach the leads to the patient. Match the lead wire color to the color-coded connectors on the top 01 the transmitter case. Refer to the ECG chapter in the UCN Operations Manualtcr details regarding electrode application, Telemetry patients are commonly ambulatory and require optimal skin preparation and lead application to minimize motion anitact. After the electrodes and lead wires have been attached, it is important to tape a loop at lead wire close to the electrode to minimize stress or pulling on the electrode itsell. This is called stress- looping. ECG monitoring begins when the telemetry receiver module detects a signal sent by a telemetry transmitter. The telemetry transmitter sends a signal as soon as its battery is installed. ECG telemetry reception requires the lollowing minimum conditions: - The telemetry receiver module must be connected to an Ultraview or PCMS monitor. either directly or through a module housing, with the power ON and a Spacelabs Medical diversity antenna connected. - ECG electrodes must be properly attached to the patient; and lead wires must be properly attached to the transmitter. - The transmitter battery must be lunctional. - The telemetry receiver module must be tuned to the telemetry transmitters lrequency (channel number). ———_—_fi— 071-0774-00 Rev. A 2-1 Ultraview D g tat Telemetry 0-‘ 5 WA All system connections must be made by Space/abs Medical personnel only. Leakage currents are not affected by the high level output. The patient is electrically isolated from the patient monitor by the HF link. HNING: Operating television receivers or other CRT displays near the transmitter (within 2 to 3 feet), or operation of some pacemaker programmers may suppress the ECG waveform, preventing OHS detection and rate counting. An erroneous asystole alarm may result. Signals resulting from devices such as Automatic Implantable Cardiac Defibrillators (AICD) may momentarily blank the ECG trace rather than display an out—of-rango signal. In such cases, it may not be apparent that the AICD has signaled and the condition of the patient should be checked. In all Instances of AICD signaling, the bedside or central will redisplay the ECG waveform within 5 seconds. ECG monitoring in telemetry is identical to hardwired ECG monitoring. Refer to lhe ECG. Arrhythmia, and STAnalysis chapters 01 the UCN Operations Manual for detailed descriptions of configurations, displays, and controls. A brief overview cl ECG monitoring lollows. Electrodes For ECG tracing with telemetry, use silver/silver—chloride electrodes or their equivatent. Always connect all the electrodes required tor a particular lead, Missing electrodes may result in the loss of ECG tracing. Refer to the ECG chapter in the UCN Operations Manual lor inlormation on placing the electrodes. Some electrodes may be subiect to large offset potentials WARNING: & - Use only Spacelabs Medical recommended electrodes. due to polarization. Recovery time after application of defibrillator pulses may be especially compromised. Squeeze bulb electrodes, commonly used for diagnostic ECG recording, may be particularly vulnerable to this effect. 2 2 0710774410 Rev. A ECG CAUTION: - Visually inspect each lead wire for obvious damage and replace them as needed. 0 Only use patient cables and lead wires specified by Spacelabs Medical. other cables and lead wires may degrade performance and may damage the monitor during delibrillation. Non-Spacelabe Medical cables and lead wires may also change the required input impedance and DC oilsel voltage, affecting monitor performance. - Do not use stainless steel electrodes. - Do not allow conductive parts of electrodes and connectors, including the reierence electrode, to contact other conductive parts, including the ground. - Poor cable dressing or Improper electrode preparation may cause Ilne isolation monitor transients to resemble actual cardiac waveiorms and inhibit heart rate alarms. Reler to the ECG chapter of the UCN Operafions Manual for details on proper electrode preparation and application. 071-0774-00 Rev. A 23 Ultravrew D tal Telemetry Full Screen 0k CentraVBedside 95669000009 Display Detail Signal detection is indicated on your monitor when an ECG signal appears next to the ECG parameter key in the zone assigned to receive the transmitted telemetry channel. The transmitters channel number is always identilied above the waveform, to the Ielt of the ECG keyu K II MON PACED/a gram—yoga 70 \‘i: VI 31m .. é £44 00m Vl/“VVWVWVV HFl=70 A=3 ll CHAN22M ‘ 1P® 00m NIBP=120/68(94) tome Spoz=se% 10:20 Split Screen Central BED “1 DAN'ELS'R HR=70 VI VVVWMMIV BED 01 DANIELS,R 00m Figure 2-1: Display Detail ECG trace for first lead Telemetry channel number ECG key for first lead OHS indicator (flashes once per detected beat) ECG lead designator Display resolution (monitor or extended) Paced operation indication (pacemaker detection is enabled) Abnormals per minule alarm Iimit' ST segment level for first lead " Abnormals in a row alarm limit’ ECG rate alarm limits; split screen oentrals display a bell symbol when alarms are enabled; bedsides display the rate alarm limits (120/40) 24 0710774470 FIGV, A ECG Abnormals per minute counter ' Current heart rate ECG lead designator for second lead ST segment level for second lead" ECG key for second lead 966666 NIBP measurements: systolic/diastolic (mean) at hourszminutes; SpOz measurement at hourszminutes (91343 only; hhzmm not seen on continuous Spoz). Depending on the patient monitor‘s display size, the title “NIBP” may not appear. Spoz SensorWatch bar: shaded area (waveform index) expands up proportionally to signal strength; horizontal line is minimum signal leveL Waveform Index (WFI) is used for displaying signal strength in SensorWatch. Q Large size bell indicates ECG alarms enabled. @ Equal sign becomes a bell when Sp02 alarms enabled. Equal sign becomes a bell when NIBP alarms enabled. ' Only appears with the MultiView l or II option in the adult mode with Arrhythmia detection enabled. "" Only appears in adult mode with the ST segment analysis option. Monitoring Paced ECG Patients ——_ To monitor paced when“: When monitoring pacemaker patients, use the paced feature to automatically 1 Touch ECG. enhance pacemaker spikes for display and eliminate them from the heart rate 2 Touch SETUP. counter. The last VES/NO setting of the paced feature you select is retained as 3 Select PACED YES. the default. If the intenral between the pacemaker pulse and the OHS complex is greater than 150 milliseconds, the beat is considered to have originated in the atria and is not classified as a paced beat. To prevent pacemaker pulses from being counted as actual beats, specialized circuitry removes the pacemaker pulses from the ECG signal and replaces them with pacemaker flags. ' - The optimal leads for monitoring paced patients may vary. In telemetry monitoring, pacemaker spikes are detected on lead ll. . ll‘ pacemaker spikes are not detected, change the electrode position. 071-0774-00 Fiev. A 2-5 Ultraview Digital Telemetry To restore default settings: 1 Touch ECG. 2 Touch SETUP. 3 Touch RESTORE SETTINGS. 4 Select YES. To change the display resolution: 1 Touch ECG. 2 Touch SETUP. 3 Select MONITOR or EXTENDED. pacemaker rate during occurrences of cardiac arrest or some arrhythmias. Do not rely entirer upon ECG rate alarms. Keep pacemaker patients under close surveillance. WARNING: E - ECG detection circuitry may continue to count the 0 The system may insert pacemaker flags into the ECG signal in response to signals that are not pacemaker pulses. Therefore, il you use a Spacelabs Medical monitor to observe pacemaker performance, you must take into account all possible sources of pacemaker flags. - Use the pacemaker manufacturer's performance analyzer as the primary means of evaluating pacemaker operation. Restoring Default Settings With the Module Configuration Manager leature, you can restore all delault settings, User-configurable options are listed in the Module Configuration Manager chapter of the UCN Operations Manual. ' - RESTORE SETTINGS changes the user—configurable options . for ALL parameters in the module. - This feature is not available for remote views. Changing the Display Resolution The MONITOR/EXTENDED key determines the display resolution of the two ECG traces. whether or not both traces are currently displayed on the monitort Table 1: Display Resolution Key Display Resolution Monitor (0.5 — 30 Hz) Extended (0,05 — 30 Hz) ' - Changing the display resolution does not change the waveform bandwidth used to analyze the ECG signals for the arrhythmia . and ST segment level. The lactovy default setting for display resolution is monitor mode, 2—6 071-0774-00 Rev. A Ultraview D tat Telemetry Hl RATE ALARM Displayed during high rate alarms tor either 10 seconds or the duration 01 the alarm. IN LEARN Displayed when the software is in learn mode. CHAN 1 & 2 LEADS OFF Displayed when lead failures preclude ECG monitoring in both ECG channels 1 and 2, The message is displayed in the wavelorm zone tor the first ECG channel. An alarm tone sounds it the module has completed its initial period ol learning and ECG processing has not been suspended, CHAN 1 LEADS OFF Displayed when a lead failure occurs on ECG channel 1 when automatic lead switching is disabled. CHAN 2 LEADS OFF Displayed when a lead failure occurs on ECG channel 2. The message is displayed in the wavetorm zone tor both ECG channels 1 and 2. L0 RATE ALARM Displayed during low rate alarms tor either 10 seconds or the duration 01 the alarm. NEW DOMINANT Displayed for 1 minute when a switch to a different dominant ECG morphology occurs. NOlSY SIGNAL Displayed in ECG channel 1 when the ECG software suspends processing on either channel because at excessive noise on the ECG signal. Alter 10 seconds in this condition, an alarm tone sounds it ECG alarms are enabled and alarm tones have not been turned OFF or suspended. This message is displayed tor the duration of the noisy signal condition plus approximately three seconds. The patient may be moving excessively. Secure the lead wires to the patient. - Check the electrodes for good skin adhesion. - Check lead wires at the transmitter tor contact. RUN ALARM Displayed whenever a RUN 01 three or more beats is detected and the ADM lN ROW limit is set lower than or equal to the number at beats in the run. This message is displayed for either 10 seconds or the duration ol the alarm. V FIB Displayed whenever ventricular fibrillation is detected, This message is displayed tor either 10 seconds or the duration at the alarm. 2-10 071-0774-00 Rev. A Sp02 (91343 only) Contents Overview ..................................... Setting Up Sp02 Monitoring . Ensuring Accurate Monitoring . Setting or Adjusting Alarm Limits. . Setting Sp02 Data Averaging Period and Sampling interval , Viewing Pulse Rate ................ . Sp02 with Inna-Aortic Balloon Pumps . Using Sp02 with Neonates . . . . Sp02 Alarm Message summary Sp02 Troubleshooting Guide , . ommxlximawm— Oven/lew Pulse oximetry enables you to noninvasively monitor a patient‘s hemoglobin oxygen saturation either continuously or opisodically. The oximetry sensor contains two light emitting diodes (LEDs) that transmit speciiic wavelengths (approximately 660 and 940 nanometers) of light that are received by a photodetector. Oxygen saturated blood absorbs light differently than unsaturated blood. Thus, the amount oi light absorbed by the blood can be used to calculate the ratio oi oxygenated hemoglobin to total hemoglobin in arterial blood. This ratio is displayed as percent Sp02. Normal values range irom 95 to 100%. WARNING: b ' A pulse oximeter should NOTbe used as an apnea monitor. - A pulse oxlmeter should be considered an earty warning device. II a trend towards patient deoxygenation is indicated, blood samples should be analyzed by a laboratory co—oximeter. your own default settings [or characteristics such as alarm limits, alarm priority, and display configuration. Refer to the Module Configuration Manager chapter in the UCN Operations Manual for further details. ' - With the Module Configuration Manager feature, you can define - Blood oxygen saturation monitoring must be performed in conjunction with ECG monitoring. The ECG lead wires of the 91343 must be connected to the patient in order to perform ECG and blood oxygen saturation monitoring. 071-0774-00 Rev, A 3-1 Ultraview D gihl Telemetry To set up Spo, monitoring: wmflm Open the battery cover and remove the battery. Confirm that the DIP switches 1 through 8 are in the correct setting (switch 7 must be set to ON for neonatal use and to OFF for adult use). Reinstall the battery and close the battery cover. Connect the Sp02 adapter Cable (P/N 700-0014-00) to the transmitter. Attach the sensor to the patient and connect the sensor cable to the SpOQ adapter cable. Initiate ECG monitoring. Touch ECG. Touch CHANNEL FORMAT. Select Sp02 ON. Setting Up Sp02 Monitoring The 91343 digital telemetry Mufti-parameter transmitter uses Spacelabs Medical sensors as well as those from other manufacturers. Refer to Accessories on page 1-13 for information concerning specific sensors. CAUTION: - Use only patient sensors specified by Spacelabs Medical. Using sensors other than those specified may degrade performance and damage the transmitter during deflbrillatlon. 0 Check the sensor site frequently. Do not allow the sensor on one site for a prolonged time, especially when 9 neonates. Refer to the sensor manufacturer's - Never attach an Spo, sensor on a limb being monitored with a blood pressure cuff or a limb with restricted blood flow. - A poorly applied sensor may give Inaccurate saturation values. - Choose a site with sufficient perfusion to ensure accurate oxlmetry values. All sensors require an adapter cable between the sensor and the transmitter. Because the adaptor cable is reusable, do not discard t| when you have finished using a disposable oximetry sensor. Disconnect the sensor cable from the adapter cable before discarding the sensor. To connect the Spoz adapter cable to the transmitter, align the cable with the notch on the front of the transmitter connector, and push the cable straight down into the transmitter. To remove the cable. press the latch release on the bottom of the cable, and pull the cable straight out. CAUTION: E - Never twist the cable. MEEGD Figure 3-1: SpOz Adapter Cable to Transmitter To enable Spoz monitoring in the 91343 digital telemetry mum-parameter transmitter. choose an averaging interval of 4, a, or 16, seconds by setting DIP switches 1 and 2 as explained in Setting 5502 Data Averaging Period and Sampling Interval on page 3-6. 071-0774-00 Rev. A Sp02 (91343 only) CHECK XX cum 22" sec WA verorw ZONE _ “a now 5 oh SpOQ=985$ 10 22 W 78 130 BED NAME PATIENT NAME ‘U ' xxvvv PACED Amto (Dom Figure 3-2: Display Zone — Full Screen Hn=xxx Azxx LEAD CHAN 2241 ‘ ECG WA VEFOHM ZONE sack/9m 10 22 7-2 Jane Doe Figure 3-3: Display Zone — Split Screen 0 Current Spoz value (percent) and episodic time oi reading. (Time is not displayed when using continuous mode 01 operation.) 9 The bell indicates that alarms are enabled (equal sign turns to a small bell when SpOZ alarms are enabled). a SensorWatch bar: Shaded area (wavelorm index. WFl) expands up proportionally to signal strength; horizontal line is minimum signal level. No shading (lowest wavelorm index) corresponds to no detected signal strength or a faulty sensor. ' - When the battery voltage in the 91345 falls below 5.5 volts, the . Spog value is displayed as 77? and the sensor watch bar is Empty- Ensuring Accurate Monitoring Each sensor requires site specific application procedures. and the lollowing general points will aid oximetry monitoring success. - Choose a site that provides proper alignment ot the LEDs and receiving photodetector, - Reduce light interference when monitoring under bright light by using a light block over the sensor. - Select a site that has unrestricted blood flow and can remain as immobile as possible to reduce or eliminate movement artilact. - Do not restrict blood flow when securing a sensor with tape. - Do not select a site near potential electrical interterence (e.g., electrical cords). 0 The SensorWatch bar should be above the minimum signal level. [171-0774-00 Rev. A 3-3 Ultraview Digital Telemetry To set or adjust Spa; alarms: Touch ECG. Touch ALARM LIMITS. Touch SPOZ ALARM LIMITS. Select SpOZ ALARMS ON. Select H|=, LO=, ALM DELAY, and MSG ALARM DELAY. Use arrow keys to adjust. mbflN-l 3-4 Setting or Adjusting Alarm Limits Pulse oximetry alarm limits and delays are based either on factory default limits or user-defined limits. The factory detault settings lor alarm limits are 100% for high and 85% for low. For alarm delays. the lactory delault settings are 15 seconds for alarm limit delay and 20 seconds for message alarm delay. Reler to the Alarms chapter in the UCN Operations Manualior details concerning UCN alarm operation. When Spoz alarms are enabled, a bell symbol will be displayed between the ‘Spoi label and the SpOz measured saturation value. When any SpOz alarm is detected. the displayed parameter value (item 1 in Figure 3-2 and Figure 3-3 on page 3-3) will blink yellow it the alarm priority is Low or Medium. and will blink red if the alarm priority is High. This is done independently 0! any other ECG or NIBP alarm indications. When Spoz alarms are enabled and the Spoz high limit is exceeded, the Spoz High=Xxx key will blink in the color of the highest priority alarm present. when the SpOg low limit is exceeded, the SpOz Low=XXX key will blink in the color at the highest priority alarm present. Refer to Directory 0! Keys - UCW and Ultraview 17GOon page 1-1. Flefer to the Module Configuration Manager chapter of the UCN Operations Manuailor Sp02 parameter tables that list available user settings and factory delaults lor this parameter. ' - The following ECG alarm messages lake priority over other . ECG and Spoz alarm messages for display, other ECG and Spoz alarm messages can be adjusted in priority by using the Module Configuration Manager. LEADS OFF NOIS V SIGNAL ECG ALAFIMS SUSPENDED ALM DELAY Key This key sets the number at seconds the system will wait before it reports that an alarm limit has been violated. When this leature is OFF, the key label will read "ALM DELAY OFF". When it is on, the label will read “ALM DELAV xx", where "xx“ is the value, in seconds, ol the delay. To set the delay time: 1. Touch ALM DELAY xx (or ALM DELAY OFF), 2. Touch the up and down arrow keys until the value is set as desired. Possible settings are OFF, 5, to, 15, 20. 25, or 30 seconds. ' - it you press the down arrow key after the lowest value has been 0 reached, the following message will appear on the prompt line: Minimum alarm delay time has been reached. - if you press the up arrow key after the highest value has been reached, the following message will appear on the prompt line: Maximum alarm delay time has been reached. [77141774410 Rev, A Spoz (91343 only) MSG ALM DELAY Key This key sets the number oi seconds the system will wait belore it issues an alarm lone after any of the lollowing messages: ' SpOz UNAVAILABLE - SpOz FAULTY SENSOR 0 SpOz SENSOR DISCONNECTED 0 Sp02 SENSOR OFF PATIENT 0 Sp02 lNSUFFlCIENT SIGNAL - SpOz AMBIENT LIGHT INTF. ° SpOz NOISY SIGNAL When this feature is OFF. the key label will read “MSG ALM DELAY OFF'C When it is ON, the label will read “MSG ALM DELAV xx" Where “xf is the value, in seconds, at the delay. To set the message delay lime: 1. Touch MSG ALM DELAY xx (or MSG ALM DELAY OFF), 2. Touch the up and down arrow keys until the value is set as desired. Possible settings are OFF, 10, 20, 30, 40. 50, or 60 seconds. ' - If you press the down arrow key alter the lowest value has been . reached, the following message will appear on the prompt line: Minimum message alan-n delay time has been reached, v ll you press the up arrow key alter the highest value has been reached, the following message will appear on the prompt line: Maximum message alarm delay time has been reached. 071-0774-00 Flev. A 3 5 Ultraview Dl To set spo, data averaging period and sampling interval, set transmitter DIP switches 1 through 4 to correct configuration tal Telemetry Setting Sp02 Data Averaging Period and Sampling Interval SpOz data averaging is used to smooth the oximetry saturation value by averaging the patient input values over 4. 5. or 16 seconds. This selection is made by setting the DIP switches 1 and 2 beneath the battery compartment in the 91343 digital telemetry multi-parameter transmitter. The default value is 5 seconds, Refer to Figure 3-4 on page 3-6. ' 0 Setting both DIP switches 1 and 2 to ON disables Spoe data transmission. - To enable SpOz, remove the battery set the selected interval, and re-install the battery. - Disabling Spoz operation in the 91543 transmitter lengthens battery lile. pens or pencils to configure the DIP switches since they may cause contamination. Avoid using sharp cutting instruments which may cause physical damage. CAUTION: g - Use care when configuring the DIP switches. Avoid using Table 1: DIP Switch 1 and 2 Settings DIP Switch 1 DIP S ' h 2 Effect OFF OFF 4 seconds averaging enabled OFF ON E! seconds averaging enabled (default) ON OFF 16 seconds averaging enabled ON 1 ON Disable srnoz operation The current setting of the Spoz averaging period may be displayed by pressing the ECG CHANNEL FORMAT key and enabling SpOz. enable enable enable enable NIBP IAEP Neonate Serviceuse 5 7 1 2 3 4 8 I ON I I I I I I I OFF 0 avera in $130 reading disable disable enable enable Sp fuelled g g "flew NIBP IABP Adult normal operation Flgure 3-4: DIP Switch Setting in Battery Compartment The sampling interval selection enables you to determine how often an SpOg measurement will be taken. Loss lrequent Spoz readings can extend the usable life of the battery. (Refer to the Ultraview Digital Telemetry Products data sheet. P/N 061-0501-xx, for more information on battery service lite.) This selection is made by setting DIP switches 3 and 4 beneath the battery compartment. The default setting is in continuous. 071-0774-00 Rev. A _“ To display heart rate from Sp02 sensor: Touch ECG. Touch SETUP. Touch RATE SOURCE. Select Sp02 ON. Select Sp02 as rate source. “fl To use with balloon pump: 1 Set transmitter DIP switch 6 to ON. utbth-e ___ To view the current setting of the IABP DIP switch: 1 Touch ECG. 2 Touch CHANNEL FORMAT. 3 Select Sp02 ON. Sp02 (91343 only) intervals. clinical practice or medical iudgement should be used in selecting continuous or episodic Sp02 monitoring made for each specific patient. CAUTION: Q - No Sp02 monitoring occurl between episodic sampling Table 2: DIP Switch 3 and 4 Settings DIP Switch 3 DIP Switch 4 Effect OFF OFF Continuous sampling (default) OFF ON 2 minute sampling interval ON OFF 5 minute sampling interval ON ON 30 minute sampling interval CAUTION: 9 - DIP switch 8 must remaln OFF for normal operation. Viewing Pulse Rate In normal operations, the heart rate for display is obtained directly lrom the acquired ECG leads or an alternate rate source. Sp02 can be used as the alternate source, if it is set for continuous measurement. When it is set for episodic measurement. Sp02 cannot be used as an alternate rate source. Sp02 with Intra-Aortic Balloon Pumps Enabling the intra-aonic balloon pump (IABP) feature informs the Sp02 software that an IABP is in use. The 91343 must differentiate between this arterial pulsations and those produced by the IABP. With the IABP feature enabled. the transmitter excludes the IABP-generated pulsations from the calculation for Sp02. The IABP teature also may be uselul with patients experiencing irregular heart rhythms. Enabling the IABP feature permits the transmitter to reject irregular pulses, providing a more accurate Sp02 measurement. ' a When the IABP feature is enabled, the pulse rate obtained from Sp02 may not match the heart rate obtained from ECG. - In cases of excessive patient motion or artifact, the accuracy of the Sp02 measurement may be compromised when the IABP feature is enabled, 0 When the IABP operation is selected, the Sp02 status key in the Channel Format menu indicates iABP. _—__—______—__————- 37 071-0774-00 Rev. A ———_——_ Ultraview Digital Telemetry 3-8 Using Sp02 with Neonates Enabling neonatal operation, by setting transmitter DIP switch 7. changes the sensor detection operation in the transmitter. improving the signal quality tor neonatal patients. This switch must be set ON lor neonatal use and set OFF for adult use. When the neonate operation is selected the SpOz status key in the Channel Format menu indicates NEO. Sp02 Alarm Message Summary WARNING: - Error messages indicate a problem or condition that may affect accurate monitoring values. Do not ignore these messages. Correct any fault before contlnulng. ' - When any Spoz alarm message is displayed, the saturation . value is immediately changed to 77? and an alarm is triggered. ll your module has been configured for an alarm using the Module Configuration Manager the parameter display will blink yellow for Low and Medium priority alarms, and will blink red for High priority alarms. An alarm will begin alter the message alarm delay time has elapsed, (Reler to the Module Configuration Manager chapter ol the UCN Operations Manual). Sp02 SENSOR DISCONNECTED Displayed when the transmitter does not detect either an adapter cable or a sensor connected to an adapter cable. it the message persists and the adapter cable is secure, replace the adapter cable. The alarm will stop after approximately 10 seconds. On remote view. there may be no audible alarm on the remote mainlrame before the local alarm stops. Sp02 FAULTY SENSOR The 91343 Spoz processor has detected a detective sensor that will require replacement. The SensorWaich bar can be used to confirm absence ol sensor output. Sp02 UNAVAILABLE Displayed when the LED and/or photcdiode have tailed. Replace the sensor and/or SDOZ adapter cable. SpOZ AMBIENT LIGHT INTF. Displayed when: - The sensor is receiving external light interlerence lrom a bright light source near the sensor. Shield the sensor from the external light source. If the condition persists lor more than 30 seconds. 77? will replace the data display. - The sensor photodiode and LEDs are misaligned on flexible sensors allowing light to enter. Realign the sensor photooiode with LEDs, - It a message appears with linger clip. replace the sensor. 07147774470 Rev. A Sp02 (91343 only) $902 INSUFFICIENT SIGNAL Displayed when: - Insufficient signal tor proper operation. - Poor sensor application or site. Correctly re-apply or reposition to a more perfused site. message the site, or apply a new sensor. Sp02 NOISY SIGNAL Displayed when: 0 The sensor signal is disturbed by motion or other interlerence. Eliminate sensor movement. The message disappears when a value is obtained. - The sensor is placed adjacent to power oords or other electrically noisy devices. Move the noisy device or move the sensor to another site. SpOZ SENSOR OFF PATIENT Displayed when: - The transmitter is unable to detect a valid sensor input signal. Check the patient tor proper sensor placement.This alarm is only available when the SpOz sensor is a reusable, linger-clip type. ' - This message is not available with disposable SPOQ sensors or . non—clip type sensors. - Tissue between the LED and photodiode is too transmissive. Il sensor placement seems correct and the message persists. try a sensor site with a thicker tissue bed. ' - Adapter cables and sensors are ordered separately through the . Space/abs Medical Supplies Products Catalog. 071—0774-00 Flsv. A 3—9 Sp02 Troubleshooting Guide Clinical Situation Possible Cause Solution No sipo2 label is displayed I sipo2 is not enabled at the 91343. I Sp02 is not enabled at the 90478 receiver. I Be sure transmitter DIP switch 1 and 2 are set correctly. I Be sure transmitter DIP switch 8 is OFF. 5p02 value displays ?’?? I Sensor not connected to patient. I Adapter cable not connected to module properly. I Sensor not connected to adapter cable. I Excessive patient motion. I Transmitter is in the initialization phase (the first 15 seconds after sensor application). I Low battery indicator constantly illuminated. I Re—aitach sensor. I Correctly connect the adapter cable. I Correctly connect the sensor. I Urge patient to remain still while reading is in progress. I Wait uniii initialization is complete. I Call qualified service person. Insuliicient signal or noisy signal I Sensor placement not optimum. I Sensor placed below blood pressure cu". I Move sensor to a site with better periusion. I Align LED with sensor photodetector. I Move sensor to an alternate limb. Intermittent or complete I Depleted battery. failure to operate I Low battery light constantly illuminated. I Replace battery. I Call qualified service person. Factors that cause significant variances in Presence ol dysfunctional hemoglobins (COHD, MetHh). sensor accuracy Presence of intravascular dyes (indocyamine green, methylene blue) depending on their concentration in the blood stream. I High ambient light level. I Electrosurgical interlerence. I Patient is significantly anemic (Hb less than 5 gm/dl) or patient has received large amounts of IV solutions. I Follow hospital procedure tor determining oxygenation in these patients. I Follow hospital procedure tor determining oxygenation in these patients. I Fleduce light levels near patient: wrap sensor with light blocking material. I Ultravlew digital telemetry is contra- indicated for electrosurgical use. I Follow hospital procedure tor determining oxygenation in these patients. 3-10 071-0774-00 Flev. A Sp02 Troubleshooting Guide (continued) Clinical Situation Possible Cause Solution No Spo2 alarms are I ECG "Leads Otf' condition exists, I Fie-attach ECG lead wires to patient and displayed I Higher priority alarm condition is resume ECG monitoring to clear present. pending ECG alarms. I Clear current alarm condition and/or reprioritize Sp02 alarms of interest in the Module Configuration Manager. I When silo2 alarms are set ON, all Sp02 alarm conditions will cause the parameter value (or ??'.7) to blink according to the alarm priority set by using the Module Configuration Manager. 071-0774-00 FIEV. A 3-11
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