LIFEPAK 15 MONITOR/DEFIBRILLATOR - Stryker

1 operating INSTRUCTIONSLIFEPAK 15 MONITOR / DEFIBRILLATOR LIFEPAK 15 MONITOR/DEFIBRILLATOROPERATING INSTRUCTIONSI mportant Information Device TrackingThe Food and Drug Administration requires defibrillator manufacturers and distributors to track the location of their defibrillators. If the device is located somewhere other than the shipping address or the device has been sold, donated, lost, stolen, exported, destroyed, permanently retired from use, or if the device was not obtained directly from Physio-Control, please do one of the following: register the device at , call the device registration phone line at , or use one of the postage-paid address change cards located in the back of this manual to update this vital tracking ConventionsThroughout these operating instructions , special text characters (for example, CAPITAL LETTERS such as CHECK PATIENT and SPEED DIAL) are used to indicate labels, screen messages, and voice HistoryThese operating instructions describe LIFEPAK 15 MONITOR/DEFIBRILLATOR devices with software revision 3306808-001 or later.

2 !USARx Only!USALIFEPAK, LIFENET, QUIK-LOOK, and QUIK-COMBO are registered trademarks of Physio-Control, Inc. CODE SUMMARY, Shock Advisory System, CODE-STAT, DT EXPRESS, LIFEPAK CR, REDI-PAK, LIFEPAK EXPRESS, SunVue, and cprMAX are trademarks of Physio-Control, Inc. Bluetooth is a registered trademark of Bluetooth SIG, Inc. CADEX is a registered trademark of Cadex Electronics Inc. Microstream, CapnoLine, and FilterLine are registered trademarks of Oridion Systems Ltd. The Oridion medical capnography in this product is covered by one or more of the following US patents: 6,428,483; 6,997,880; 5,300,859; 6,437,316 and their foreign equivalents.

3 Additional patent applications pending. PC Card is a trademark of the Personal Computer Memory Card International Association. Masimo, the Radical logo, Rainbow, and SET are registered trademarks of Masimo Corporation. EDGE System Technology is a trademark of Ludlow Technical Products. Formula 409 is a registered trademark of The Clorox Company. Specifications are subject to change without notice. 2007-2010 Physio-Control, Inc. All rights reserved. Publication Date: 05/2010 MIN 3306222-002 2007-2010 Physio-Control, 15 MONITOR/DEFIBRILLATOR operating InstructionsiiiCONTENTS1 PrefaceIntroduction.

4 1-3 Intended of Operation ..1-52 Safety InformationTerms ..2-3 General Dangers and Warnings ..2-33 Basic OrientationFront View ..3-3 Back View ..3-13 Batteries ..3-15 Home ..3-21 Options .. MonitoringMonitoring the ECG ..4-3 Acquiring a 12-Lead ECG ..4-15 Monitoring SpO2, SpCO, and SpMet ..4-25 Monitoring Noninvasive Blood Pressure ..4-37 Monitoring Invasive Pressure ..4-54 Monitoring Continuous Sign and ST Segment Trends ..4-665 TherapyGeneral Therapy Warnings and Cautions ..5-3 Therapy Electrode and Standard Paddle Placement ..5-4 Automated External Defibrillation (AED) ..5-7 Manual Defibrillation.

5 5-22 Synchronized Cardioversion Procedure ..5-27 Noninvasive Pacing ..5-32 Pediatric ECG Monitoring and Manual Mode Therapy Procedures ..5-396 Paddle Accessory OptionsQUIK-COMBO Therapy Electrodes ..6-3 Standard 15 MONITOR/DEFIBRILLATOR operating Instructions7 Data ManagementPatient Records and Reports ..7-3 Memory Capacity ..7-9 Managing Current Patient Records ..7-10 Managing Archived Patient Records ..7-118 Data TransmissionAbout Transmitting Patient Records and the Monitor for Transmission ..8-4 Using Bluetooth Wireless a Direct Reports ..8-12 Considerations When Transmitting Data ..8-14 Troubleshooting Tips.

6 8-159 Power AdapterBasic Orientation ..9-3 Using the Power ..9-1010 Maintaining the EquipmentGeneral Maintenance and Testing ..10-3 Battery Maintenance ..10-12 Cleaning the the Paper ..10-17 General Troubleshooting Tips ..10-18 Service and Repair ..10-22 Product Recycling Information ..10-23 Warranty ..10-23 Accessories ..10-24 Appendix A: Specifications and Performance CharacteristicsAppendix B: Screen MessagesAppendix C: Shock Advisory SystemAppendix D: Electromagnetic Compatibility GuidanceAppendix E: Symbols 2007-2010 Physio-Control, 15 MONITOR/DEFIBRILLATOR operating Instructions1-11 PREFACEThis chapter provides a brief introduction to the LIFEPAK 15 MONITOR/DEFIBRILLATOR and describes the product s intended.

7 Page 1-3 Intended Use .. 1-4 Modes of Operation .. 1-5 PREFACE1 2007-2010 Physio-Control, 15 MONITOR/DEFIBRILLATOR operating Instructions1-3 IntroductionThe LIFEPAK 15 MONITOR/DEFIBRILLATOR is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. These operating instructions include information and procedures related to all features of the LIFEPAK 15 MONITOR/DEFIBRILLATOR . Your LIFEPAK 15 MONITOR/DEFIBRILLATOR may not have all of these features. These operating instructions describe the operation of the LIFEPAK 15 MONITOR/DEFIBRILLATOR when the factory default settings are used.

8 The factory default settings for all setup options are identified in Table A-5 on page A-16. Your device may be set up with different default settings, based on your protocols. For information about changing default settings, see the LIFEPAK 15 MONITOR/DEFIBRILLATOR Setup Options provided with your device. IMPORTANT! Some LIFEPAK 15 MONITOR/DEFIBRILLATOR accessories are not interchangeable with accessories that are used with other LIFEPAK monitor/defibrillators. Specific accessory incompatibilities are noted in the related 15 MONITOR/DEFIBRILLATOR operating InstructionsIntended UseIntended UseThe LIFEPAK 15 MONITOR/DEFIBRILLATOR is intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified on page A-12.

9 The LIFEPAK 15 MONITOR/DEFIBRILLATOR is designed to be used during ground transportation except when specified otherwise. Monitoring and therapy functions may only be used on one patient at a time. Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older. For additional intended use information, and information about the indications and contraindications of the monitoring and therapy functions, see the individual sections identified below. ECG MonitoringSee page 4-3 Standard feature 12-Lead ElectrocardiographySee page 4-15 Optional SpO2, SpCO.

10 And SpMet MonitoringSee page 4-25 Optional Noninvasive Blood Pressure MonitoringSee page 4-37 Optional End-Tidal CO2 MonitoringSee page 4-45 Optional Invasive Pressure MonitoringSee page 4-54 Optional Temperature MonitoringSee page 4-61 Optional Vital Sign and ST Segment TrendsSee page 4-66 Optional Automated External DefibrillationSee page 5-7 Standard feature Manual DefibrillationSee page 5-22 Standard feature Noninvasive PacingSee page 5-32 Standard featurePREFACE1 2007-2010 Physio-Control, 15 MONITOR/DEFIBRILLATOR operating Instructions1-5 Modes of OperationThe LIFEPAK 15 MONITOR/DEFIBRILLATOR has the following modes of operation: AED mode for automated ECG analysis and a prompted treatment protocol for patients in cardiac arrest.