Hidalgo EQ001 Equivital Vital Signs Monitor type EQ-01-001 User Manual Application Guide

Hidalgo Limited Equivital Vital Signs Monitor type EQ-01-001 Application Guide

Contents

Application Guide

Stable Block at The Grange, 20 Market Street, Swavesey, Cambridge, CB4 5QG Tel: +44 (0) 1954 233430 Fax: +44 (0) 1954 233431 www.hidalgo.co.uk EQUIVITAL™ EQ-01 VITAL SIGNS MONITOR USER APPLICATION GUIDE Draft: D Date: 02nd June 2006 For Support or further information on this product contact: Customer Support Hidalgo Limited Stable Block at The Grange 20 Market Street Cambridge CB4 5QG United Kingdom www.hidalgo.co.uk Tel: +441954 233430 email: equivitalsupport@hidalgo.co.uk
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 2 of 14 CONTENTS What is the Equivital Monitor Used For: .................................................................................................... 4 What does the Equivital Vital Signs Monitor Consist Of:.........................................................................5 Fitting Instructions........................................................................................................................................ 5 Recharging or Changing Batteries on the SEM ...................................................................................... 8 Switching the Sensor On and Off............................................................................................................ 10 Washing and Cleaning ............................................................................................................................ 10 Accessories................................................................................................................................................ 10 Repair and Service ................................................................................................................................... 11 Technical Specifications .......................................................................................................................... 11 FCC Compliance and Advisory Notice (US Markets) .......................................................................... 13
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 3 of 14 Explanation of Symbols Within this manual the following symbols are used to indicate warnings and precautions a user should take when using this device: A warning is shown within a highlighted box and includes a symbol Failure to follow the warning may comprise the safe operation of the device and can lead to a risk of injury. A precaution is noted in a highlighted box. Failure to follow a precaution may lead to a reduction in performance of the device when in use. Before using Equivital™ Please observe the following warnings and precautions: Warnings • IF YOU ARE UNCLEAR AS TO WHY YOU ARE BEING ASKED TO WEAR THIS DEVICE PLEASE CONSULT THE HEALTH CARE PROFFESIONAL OR OCCUPATIONAL WELFARE PERSONNEL RESPONSIBLE BEFORE USE. • THE EQUIVITAL™ DEVICE MAY BE USED TO MONITOR INDIVIDUALS IN THE WORKPLACE. WHEN USED IN THIS MANNER THE DEVICE MUST BE INTEGRATED INTO THE OPERATING ORGANISATIONS SAFETY AND RISK MANAGEMENT PROCEDURES. YOU SHOULD RECEIVE APPROPRIATE TRAINING FROM YOUR ORGANISATION BEFORE USING THIS DEVICE • USE OF THE DEVICE DOES NOT JUSTIFY THE USER OR ORGANISATION TO TAKE ADDITIONAL SAFETY RISKS OR TO REDUCE LEVEL OF CARE. • THIS DEVICE DOES NOT AUTOMATICALLY CALL EMERGENCY SERVICE ASSISTANCE. • DO NOT APPLY SENSOR TO BROKEN, DAMAGED OR IRRITATED SKIN. • REMOVE SENSOR IMMEDIATELY IF SKIN IRRITATION OR RASHING OCCURS. • DO NOT ATTEMPT TO CONNECT ANY CABLES TO THE EQUIVITAL DEVICE WHEN WORN ON BODY- THIS INCLUDES HIDALGO SUPPLIED BATTERY CHARGING DEVICE. ALWAYS REMOVE THE DEVICE BEFORE CHARGING.
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 4 of 14 • IF YOU HAVE AN IMPLANTED DEFIBRILLATOR OR PACEMAKER DO NOT USE THIS DEVICE. IF YOU WEAR OR USE OTHER MEDICAL EQUIPMENT PLEASE CONTACT YOU HEALTH CARE PROFESSIONAL BEFORE USING THIS DEVICE. • USE ONLY THE HIDALGO PROVIDED BATTERY CHARGER AND BELT ASSEMBLIES WITH THE DEVICE. THE SAFE USE OF THE DEVICE IS ONLY GUARANTEED WITH THESE ACCESSORIES. A FULL LIST OF ACCESSORIES IS PROVIDED AT THE REAR OF THIS DOCUMENT Precautions • DO NOT USE LOTIONS, OILS, PERFUMES, DEODORANT OR POWDER ON THE AREA WHERE THE SENSOR BELT IS BEING APPLIED • EACH TIME YOU USE THE SENSOR INSPECT THE BELT AND CASE UNIT FOR SIGNS OF DAMAGE (TEARS/ CRACKS ETC). IF ANY DAMAGE IS IDENTIFIED DO NOT USE THE SENSOR UNTIL THE DAMAGED PART HAS BEEN REPLACED • TO GET MAXIMUM PERFORMANCE FROM THE SYSTEM YOU SHOULD REPLACE THE BELT HARNESS AFTER 25 WASHES. The Equivital™ Vital Signs Physiological Monitor is a non-invasive ambulatory monitoring wireless telemetry device intended to allow monitoring of a users vital signs physiology in environment’s where access to traditional clinical care facilities may be limited or impractical (for example in the workplace or outdoors) and justification exists for such monitoring. The device maybe used by persons operating in circumstances where an increased risk of physical trauma exists due to the environment in which the user is placed. Typically these environments may be found within personnel working in the military, public safety and hazardous plant workplaces. The device may also be used for the collection of ambulatory physiology for general research purposes in application such as sports or human performance medicine. The device offers continuous monitoring of two views of the user’s heart electrical activity (ECG) and respiratory breathing frequency inferred from thoracic cavity movement and uses this data to derive a Heart and Breathing Effort Rate. The sensor also provides additional information: • an indication of the users activity level (none, low or high) derived from a movement detection sensor. What is the Equivital Monitor Used For:
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 5 of 14 • body orientation. • chest skin surface temperature. • alternate secondary measurement of heart rat • alternate secondary measurement of respiration effort • indications and alerts if physiology exceeds predefined boundaries. The device consists of two items: A sensor electronics module (SEM) which contains a battery , electronics and software in order to measure the vitals signs signals off the body. A belt harness which holds the SEM onto the body and contains fabric electrodes in order to contact to the user skin. Selecting the Correct Belt Size The following sizing chart provides a guideline on how to select the correct belt size to use Belt Size Shirt Size Chest Circumference S S 33-37 M M 37-41 L L 41-45 XL XL 45-49 Some variation may exist for uses at the size boundaries in which case it is recommended to go for the larger sized belt. Applying the Belt 1. Pass adjuster strap through loop of shoulder strap What does the Equivital Vital Signs Monitor Consist Of:Fitting Instructions
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 6 of 14 2. Place shoulder strap over left arm and then place chest strap around the waist. Then pull the adjuster band with the right hand so that it comfortable meets the buckled end (held in the left hand), on the right hand side of the torso. 3. Loop the adjuster band through the buckle and tighten just enough to take out excess slack. 4. Straighten the band so the centre section sits centrally on the chest. 5. Tighten strap by holding the buckle with the left hand and pulling the adjuster strap with the right hand. The belt should be a snug fit to the body 6. When tensioned correctly, the strap must be comfortable and should not restrict the users chest movement. As a guide, it should be possible to easily place one finger under the strap when tightened. 7. To adjust the upper strap, remove from the shoulder and lengthen/shorten as necessary. 8. Replace strap over shoulder and adjust rear lower section such that it sits centrally on the back between the buckles.
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 7 of 14 9. To ensure that the strap is now positioned and tensioned correctly, extend arms to the side and raise and lower them a few times. Now moisten the skin under the three electrode sites with saliva or water which accelerates the electrode to skin connection and improves in the initial few minutes after application. Attaching the “SEM” Electronics Unit and Final Adjustments Take the SEM electronics module: The rear of the SEM electronics unit has simple “snap” stud connectors which allow it to be connected to the sensor If this is the first time you have used the SEM or you have just completed recharging the SEM. Place the activation connector into the hole on the front of the unit. Activation connector
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 8 of 14 Once the device is activated, hold the device for approximately six seconds. The units internal vibration alerter will operate with three short pulses indicate that it is correctly operating. In order to verify transmission from the sensor is being received remotely you will need to check or confirm with the receiving station or monitoring point your sensor talks to. (This will vary from system to system so ask your system operator or health care practioner if you are unsure) Now take the unit and connect each snap in turn making sure all have been connected. Finally adjust the location of the sensor belt for comfort and make sure the SEM unit is centrally located on the chest as shown below: The sensor unit SEM comes with two options for powering the unit, a rechargeable cell, or replaceable AAA/LR03 batteries. The option you have will depend on what type of device was specified when it was purchased. Changing the AAA Batteries Remove the rear battery door by sliding it down and then lifting it out Recharging or Changing Batteries on the SEM
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 9 of 14 Fit the batteries into the battery compartment observing the polarity marking inside the case and replace the case. • USE ONLY PRIMARY NON-RECHARGABLE (LR03 AAA) ALKALINE CELLS. RECHARGEABLE AAA CELLS SHOULD NOT BE USED. Recharging the SEM Remove the activation bung and attach the charger unit cable to the connector. The charger will indicate a red light when charging and green when charged. Only connect the charger power plug to the socket after you have attached it to the SEM. Failing to do this can give false indications of charge on the charger light. In order to maximise the rechargeable battery lifetime it is recommended to avoid leaving the unit connected to the charger once fully charged.
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 10 of 14 If you want to stop using the sensor, or only use it intermittently – remove power by taking the activation bung out of its hole. • REMOVE THE AAA BATTERIES FROM THE DEVICE IF IT WILL NOT BE USED FOR SOME TIME (>10DAYS). THIS IS TO REDUCE THE RISK OF THE CELLS LEAKING AND CORODING THE BATTERY CONTACTS SEM Wipe the SEM clean with a damp cloth and leave to dry normally Belt Wash the belt in a cold wash (40°C) using a mild non biological detergent. • DO NOT TUMBLE DRY THE BELT – THIS WILL REDUCE THE LIFE OF THE BELT • USE ONLY THE FOLLOWING ACCESSORIES. Battery Charger Hidalgo Part Number: EQ-ACC-01 - Mascot 2240 LI(UK Plug) EQ-ACC-02 - Mascot 2240 LI (US Plug) Switching the Sensor On and OffWashing and CleaningAccessories
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 11 of 14 EQ-ACC-03 - Mascot 2240 LI (EU Plug) Chest Belt Hidalgo Part Number: EQ01-020 (/S/M/L/XL) • THERE ARE NO USER SERVICEABLE PARTS IN THE DEVICE. SHOULD YOU REQUIRE SERVICE OR REPAIR PLEASE CONTACT HIDALGO Device Classification Shock Protection : Type BF Applied Part , Internally Powered Equipment Enviromental Protection: IPx0 (unprotected) Flammable Gas Protection: Unprotected Mode of Operation: Continuous FDA Device Classification: Class II EU Device Classification: Class IIb Chest Harness /Belt Size (circumference): Small: 40mm x 108mm Medium: 40mm x 116mm Large: 40mm x 124mm Extra Large:40mm x 131mm Weight: 80g Operating temperature: -10°C to +55°C Operating Humidity: 10% to 75% RH Non-Condensing Storage Temperature: -20°C to +65°C Storage Humidity: 5% to 90% RH Non-Condensing Air Pressure: 570hPA – 1060hPA Repair and ServiceTechnical Specifications
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 12 of 14 Sensor Electronics Module • General Size (overall dimensions): 123mm x 75mm x 14mm Weight: 75g Power: 2 x 1.5v AAA LR03 Alkaline cells or 3.7V 740mA Li-ION rechargeable cell Operating temperature: -10°C to +55°C Operating Humidity: 0% to 95% RH Non-Condensing Storage Temperature: -20°C to +65°C Storage Humidity: 0% to 95% RH Non-Condensing • ECG No of leads: 2 Sampling frequency: 256 Hz Resolution: 10 bits Voltage range: +/- 5mV CMRR: >85 dB Frequency Range: Diagnostic Setting : 0.05 – 85 Hz (3dB points) Monitor/Ambulation Setting : 5Hz – 85Hz (3dB points) Heart Rate Calculation Frequency: 15 seconds • Impedance Respiration Effort Measurement type: Bipolar Sampling frequency: 25.6 Hz Resolution: 10 bits Modulation: 50 KHz Drive Current: 200 µA Frequency Range: 0.05 – 7 Hz Respiration Rate Reporting Frequency: 15 seconds • Chest Expansion Respiration Effort Measurement type: Resistive strain gauge Sampling frequency: 25.6 Hz Resolution: 10 bits Frequency Range: 0.05 – 7 Hz Respiration Rate Reporting Frequency: 15 seconds • Temperature Sampling frequency: 0.25Hz Resolution: 10 bits Range: 10°C - 45°C Sensor Accuracy: <35.8C and > 41C +/- 0.3 C 35.8C to 37C +/-0.2C 37 to 39 C +/- 0.1C 39C to 41 C +/- 0.2 C
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 13 of 14 Measurement type: Thermistor Temperature Reporting Frequency: 15 seconds Radio – Type 0 Low Power Pan Frequency: 40.68MHz Modulation: Binary FSK Data Rate: 2400 Baud Modulation: +/- 4KHz Radio – Type 1 Bluetooth Frequency: 2401 – 2480MHz Modulation: TDD GFSK (BbT -0.5) Data Rate: 1MBPS Carrier Spacing: 1 MHz No of Channels: 79 Tx Power: Class 2/+4dBm Max Electromagnetic Compatibility This device has been designed to meet the relevant radio and electromagnetic interference standards for the countries its is used in. A risk remains however, as for all radio based devices, that interference may occur either from or to the device. If you experience unwanted interference increase the physical separation between the devices. We recommend a separation of 0.5 meter or greater between the SEM device and other wireless devices. If you have specific concerns about the devices compatibility or experience problems which cannot be resolved by increasing separation of the devices, please contact Hidalgo. • IF YOU ARE ENTERING A FACILITY WHERE INTERFERENCE MAY BE A PARTICULAR CONCERN (EG: A HOSPITAL OR HAZARDOUS PLANT ENVIROMENT ) CONTACT THE PERSON IN CHARGE OF THE FACILITY TO CHECK IF ANY SPECIAL PRECAUTIONS NEED TO BE TAKEN. This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can FCC Compliance and Advisory Notice (US Markets)
USER APPLICATION GUIDE Draft: D 02nd June 2006 Page: 14 of 14 radiate radio frequency energy and, if not installed and used in accordance with the instructions for use, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures: • Reorient or relocate the receiving antenna. • Increase the separation between the equipment and the receiver. • Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. • Consult the dealer or an experienced radio/television technician for help. This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) these devices must accept any interference received, including interference that may cause undesired operation. FCC ID: T85EQ001

Navigation menu