Elsevier

Resuscitation

Volume 85, Issue 4, April 2014, Pages 560-566
Resuscitation

Simulation and education
Comparing three CPR feedback devices and standard BLS in a single rescuer scenario: A randomised simulation study

https://doi.org/10.1016/j.resuscitation.2013.10.028Get rights and content

Abstract

Background

Efficiently performed basic life support (BLS) after cardiac arrest is proven to be effective. However, cardiopulmonary resuscitation (CPR) is strenuous and rescuers’ performance declines rapidly over time. Audio-visual feedback devices reporting CPR quality may prevent this decline. We aimed to investigate the effect of various CPR feedback devices on CPR quality.

Methods

In this open, prospective, randomised, controlled trial we compared three CPR feedback devices (PocketCPR®, CPRmeter®, iPhone app PocketCPR®) with standard BLS without feedback in a simulated scenario. 240 trained medical students performed single rescuer BLS on a manikin for 8 min. Effective compression (compressions with correct depth, pressure point and sufficient decompression) as well as compression rate, flow time fraction and ventilation parameters were compared between the four groups.

Results

Study participants using the PocketCPR® performed 17 ± 19% effective compressions compared to 32 ± 28% with CPRmeter®, 25 ± 27% with the iPhone app PocketCPR®, and 35 ± 30% applying standard BLS (PocketCPR® vs. CPRmeter® p = 0.007, PocketCPR® vs. standard BLS p = 0.001, others: ns). PocketCPR® and CPRmeter® prevented a decline in effective compression over time, but overall performance in the PocketCPR® group was considerably inferior to standard BLS. Compression depth and rate were within the range recommended in the guidelines in all groups.

Conclusion

While we found differences between the investigated CPR feedback devices, overall BLS quality was suboptimal in all groups. Surprisingly, effective compression was not improved by any CPR feedback device compared to standard BLS. All feedback devices caused substantial delay in starting CPR, which may worsen outcome.

Introduction

Cardiac events are a leading cause of death worldwide, despite our best life support efforts, and outcome after cardiac arrest is still poor.1, 2, 3 Several investigations strongly suggest that efficiently performed basic life support (BLS) is the only sufficient and immediately available treatment for cardiac arrest and may improve long term outcome.1, 4 However, rescuers’ cardiopulmonary resuscitation (CPR) performance – particularly external chest compression quality – decreases rapidly over time.5 Thus a number of devices providing audio-visual feedback during chest compressions (CPR feedback devices) have been introduced in an effort to improve BLS quality.2, 4, 6, 7 Such CPR feedback devices can be used by medical staff and trained laypersons alike even if manual defibrillators or automated external defibrillators (AED) are not available, or defibrillators without CPR feedback are used.8, 9, 10

These devices seek to become a clinical standard, but at present, data on the improvement of resuscitation quality using such devices are insufficient, and no direct comparison of such CPR feedback devices has been performed. Because of the lack of performance data, we compared three CPR feedback devices (Zoll PocketCPR®, Laerdal CPRmeter®, iPhone app Zoll PocketCPR®) with standard BLS without feedback in simulated single-rescuer BLS without a defibrillator in an 8-minute scenario.

In a previous study on CPR feedback devices integrated into an AED we showed an improvement in effective compression of about 15% compared to standard BLS.6 The aim of our current study was to investigate whether standalone CPR feedback devices improve CPR quality compared to standard BLS.

Therefore, our 0-hypothesis was that CPR feedback devices would not improve chest compression efficiency compared to standard BLS in a group of trained lay rescuers over time.

Section snippets

Study protocol

This open, prospective, randomized, controlled parallel group study was approved by the Ethics Committee of the Medical University of Vienna (EK No. 1676/2012). Over a period of four weeks, we recruited 240 medical students at the compulsory BLS course in their fifth semester of medical school. Exclusion criteria were upper extremity injuries and pregnancy. All study participants received standardized BLS training prior to the investigation. It was communicated to the study participants that

Results

Out of 244 potential study participants, one was ineligible for our investigation due to pregnancy and three due to previous musculoskeletal upper extremity injuries (Fig. 1). Demographic characteristics of the 240 study participants in the 4 study groups are shown in Table 1. No dropouts occurred after randomization. There was no significant difference in real life CPR experience and resuscitation training between the groups. The mean time of the study participants’ training, until they felt

Discussion

This study investigated the efficiency of chest compressions comparing three CPR feedback devices (Zoll PocketCPR®, Laerdal CPRmeter®, the iPhone app Zoll PocketCPR®) and standard BLS without feedback in a simulated setting. We confirmed our 0-hypothesis that chest compression efficiency did not improve through the application of any of the standalone CPR feedback devices compared to standard BLS.

The effective compression (EC), a compound parameter to easily compare chest compression quality,

Conclusion

Despite several differences between the CPR feedback devices and standard BLS, none of the devices achieved an improvement in EC or ECR as markers for chest compression quality compared to standard BLS without feedback. CPR quality with the PocketCPR® was even significantly reduced due to insufficient decompression and incorrect compression point.

All CPR feedback devices caused delay in CPR start and may worsen outcome. PocketCPR® was the only device that significantly improved chest

Conflict of interest statement

None of the authors has a conflict of interest. The Laerdal CPRmeter® was provided by Laerdal free of charge during the period of the study. Apart from this, only departmental support was used for the study. Neither Zoll Medical nor Laerdal reviewed or revised the manuscript at any stage.

Acknowledgements

We would like to thank all medical students for their participation in our study. In addition, we would like to thank Prof. Wilhelm Behringer for providing a Thumper®, Florian Schachinger, Julian Voitl and Paul Bsuchner who helped with the data collection and Emily Lemon for the English proofreading.

References (27)

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A Spanish translated version of the abstract of this article appears as Appendix in the final online version at http://dx.doi.org/10.1016/j.resuscitation.2013.10.028.

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