If you are searching for a cost-effective solution for your medical team, E LECOTEK has the right equipment for you.
The Lifepak 20e defibrillator, monitor and pacer is designed for indoor use. It is compact and lightweight for easy carrying, and monitoring ECG and pulse-oximetry. Because of its small footprint and its highly intuitive design for quick and effective AED use, it is the ideal crash cart defibrillator/monitor. The large screen with color LCD allows easy viewing from many angles. The optional CodeManagement Module provides etCO2 monitoring, WiFi, and the trueCPR port.
The following table shows the main capabilities of the Cardiac Biphasic Defibrillator/Monitor.
The Monitor provides monitoring of the following parameters:
The Monitor can record, print, or transmit a CODE SUMMARY™ Critical Event Record.
The defibrillation unit provides an AED mode for BLS teams, and an advanced mode for ALS teams.
Manual Defibrillation for ALS Teams
trueCPR™ port with optional CodeManagement Module
Noninvasive Transcutaneous Pacing (NTP) for ALS teams
Optional CodeManagement Module provides wireless communication.
The LIFEPAK Monitor is the ideal portable monitoring device for moderately ill patients. It can monitor 3-Lead ECG and pulse-oximetry (SpO2). With the optional CodeManagement Module it can also measure end-tidal CO2.
The internal nickel-metal hydride battery is rechargeable and intended to be used for standby operation. A new, fully charged battery provides approximately 90 360-joule discharges, 70 minutes of pacing, or approximately 120 minutes of continuous monitoring before the defibrillator turns off.
The LIFEPAK Defibrillator uses a biphasic waveform for defibrillation. Research has shown that it has greater shock efficacy in patients with ventricular fibrillation (Review by Nichol et al., JACC, Dec. 2017).
Depending on the operating team (BLS or ALS team) the LP20e Defibrillator can be run in different modes:
- AED Mode
- Manual Mode
- Synchronized Cardioversion
While the front console is closed (see picture) a simple 1-2-3 operation guides the BLS user through the process of the defibrillation. The default settings are consistent with 2005 American Heart Association (AHA) and European Resuscitation Council (ERC) guidelines. Prior to following the commands, the BLS user must verify that the patient is in cardiac arrest (unconscious, no respiration, no pulse). The American Heart Association recommends that AEDs must not be used in pediatric patients younger than eight years of age.
The ANALYZE button activates the Shock Advisory System (SAS) and the AED mode which guides the user with voice and visual prompts through each step.
According to the LP20e manual, the electrodes must be placed in the anterior-lateral (Lead II) position. The shock advisory algorithm does not reliably work with electrodes in the anterior-posterior position.
Manual mode can be entered by pressing the Manual button located in the lower left corner of the door. This opens the door and automatically provides access to manual defibrillation and pacing. The clear and instructive front panel provides all important buttons in one place.
For pediatric patients (younger than 8 years of age) the energy levels are calculated per kilogram body weight: First shock 2 J/kg, second shock 4 J/kg, subsequent shocks =4 J/kg, maximum 10 J/kg or adult dose. For further information, please refer to Pediatric Cardiac Arrest Algorithm - 2015 Update (PDF).
An illuminated AED MODE LED indicates that the Continuous Patient Surveillance System (CPSS) is activated. It automatically evaluates the patient's ECG for a potentially shockable rhythm, i.e. ventricular tachycardia (VT) or ventricular fibrillation (VF). If a shockable rhythm is detected, the PUSH ANALYZE prompt occurs.
In case of an in-hospital cardiac arrest, skilled personnel trained in ACLS must exclude contraindications as follows:
- Dysrhythmias due to enhanced automaticity (digitalis toxicity, catecholamine-induced arrhythmia)
- Multifocal atrial tachycardia
In these conditions cardioversion is associated with a higher incidence of post-shock VT and VF. (AHA Guideline 2015 Update for CPR and ECC)
The unit is also capable of synchronized defibrillation (SYNC ON) by discharging the shock with the next detected R wave. This helps to avoid the vulnerable T-wave segment of the cardiac cycle. Indications for electrical cardioversion include supraventricular tachycardia (SVT), atrial fibrillation or flutter, and VT with pulse.
cprMAX technology is designed to allow resuscitation protocols to maximize the quantity of CPR administered during treatment with an AED. AED protocols are aligned with the AHA and ERC Guidelines when the setup options are set as follows:
- Initial CPR: OFF
- PreShock CPR Time: OFF
- CPR Times: Default setting is 120 seconds
- Stacked Shocks: OFF
- Pulse Check: NEVER
According to AHA 205 guidelines, CPR should be provided while the AED pads are applied and until the AED is ready to analyze the rhythm. For witnessed adult cardiac arrest when an AED is immediately available, it is reasonable that the defibrillator be used as soon as possible.
Depending on local hospital protocols, it might be useful to use CPR FIRST setting that prompts the user to perform CPR immediately after the defibrillator is powered on. The AED will also prompt, IF YOU WITNESSED THE ARREST, PUSH ANALYZE, which provides the opportunity to end CPR early and proceed directly to analysis.
After each delivery of a shock, the device will advise to START CPR again. A countdown timer continues for the duration specified in the CPR TIME setup option (default 120 sec). Afterwards, the PUSH ANALYZE command is displayed again.
The AHA recommends minimal interruptions of chest compressions. A pulse check should not take longer than 10 seconds. If the rescuer cannot detect a pulse within that time-period, chest compressions should be started. Ideally, the pulse check is performed simultaneously with the check for no breathing or only gasping.
Non-invasive Transcutaneous Pacing (NTP)
In case of severe bradycardia, the LIFEPAK Defibrillator can deliver two types of pacing:
- Demand pacing
- Non-demand (asynchronous) pacing
The QUIK-COMBO electrodes are attached to the thorax in an anterior-lateral (apical) or anterior (pre-cordial) and posterior position. The LIFEPAK Defibrillator pacer allows for continuous adjustment of the output current between 0 and 200 mA. The pacing rate can be set between 40 and 170 pulses per minute (ppm).
Data Management and Transmission of Data
Typically, the data memory of the LP20e can store up to 100 single waveform reports. Patient reports are stored as a CODE SUMMARY™ Critical Event Record, which includes patient information, event and vital signs logs, and waveforms associated with events, e.g. defibrillation. Patient reports can be transmitted to a PC-compatible computer via wireless, infrared communication (IrDA) or wireless LAN connection with the optional CodeManagement Module. Alternatively, the report can be printed with the in-built 50 mm printer.
Optional CodeManagement Module
The optional CodeManagement Module provides a port for end-tidal CO2, TrueCPR Device Port, and wireless connectivity (LAN and LIFENET server). It is powered by its own Li-Ion battery. The TrueCPR device port transfers data from the TrueCPR Coaching Device to the LIFENET System. It helps to optimize the quality and performance of manual CPR by providing feedback in real time and after the event.
Please note: When the CodeManagement Module is attached to the LP20e, the IrDA connection is disabled. The docking station cannot be used with the CodeManagement Module.