Device-led versus human-led feedback on chest compressions for cardiopulmonary resuscitation and providers experience and preference: a randomised crossover study

Abstract

Background:  High cardiopulmonary resuscitation (CPR) quality is associated with better patient survival from cardiac arrest. However, CPR providers may not have an accurate perception of the depth and rate of their chest compressions (CC). Realtime feedback during resuscitation improves CPR quality compared to no feedback. Evidence comparing audio-visual feedback device (AVF) and team leader’s feedback (TLF) in improving CPR performance is limited and conflicting.  Methodology:  We performed a randomized crossover study to evaluate CC performance with AVF and TLF. Seventy participants performed CC for 1 minute on a CPR manikin connected to ZOLL R series defibrillator with CPR-sensing capability in a randomised crossover sequence. We interviewed participants to explore their perception and preference with both feedback methods. Results:  Mean CC rate was higher with AVF than with TLF (121.8 min -1  ± 17.7 vs. 117.4 min -1  ± 13.5,  p  = 0.005). There was no significant difference in proportions of participants performing CC within the recommended rate of 100-120 beats per minute between AVF and TLF (48.6% and 51.4%,  p  = 0.824). Overall, CC depth was below the recommended target regardless of feedback method with mean CC depth of 4.4 cm ± 0.8 in AVF and 4.3 cm ± 0.9 in TLF respectively ( p  = 0.479). Most participants felt that TLF was easier to follow, more motivating and preferable compared to AVF. Those who preferred TLF performed CC at rates above the recommended range with AVF compared to TLF (124.1 min -1  ± 19.4 versus 118.2 min -1  ± 14.9,  p  = 0.004). Conclusion:  A well-trained team leader is as effective as an AVF device in leading high-quality CC.  CPR providers’ performance may be influenced by their preferred feedback method.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

NMRR-19-1174-48443

Funding Statement

The author(s) received no specific funding for this work.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Medical Research Ethics Committee of University Malaya Medical Centre and the National Medical Research of Malaysia gave ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable.

Yes

Data Availability

The data underlying the results presented in the study are available from the corresponding author via email at nuraliyah@ummc.edu.my

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