Does the use of cardiopulmonary resuscitation feedback devices improve the quality of chest compressions performed by doctors? A prospective, randomized, cross-over simulation study.


Journal

Cardiology journal
ISSN: 1898-018X
Titre abrégé: Cardiol J
Pays: Poland
ID NLM: 101392712

Informations de publication

Date de publication:
2019
Historique:
received: 16 07 2018
accepted: 22 07 2018
revised: 24 08 2018
pubmed: 30 8 2018
medline: 29 7 2020
entrez: 30 8 2018
Statut: ppublish

Résumé

The aim of the study was to compare the quality of chest compressions (CCs) carried out with and without the use of the TrueCPR device during simulated cardiopulmonary resuscitations conducted by trainee doctors. The study was a prospective, randomized, cross-over simulation study. The study involved 65 trainee doctors who were tasked with performing a 2-min cycle of uninterrupted CCs under conditions of a simulated cardiopulmonary resuscitation of adults. CC were carried out in two scenarios: with and without TrueCPR chest compression support. Participants did not have experience in the use of CCs prior to this study. The depth of compressions in regard to CC techniques were varied by 45 mm (IQR 43-48) for manual CC and 53 mm (IQR 51-55) for the TrueCPR device (p < 0.001). The incidence of CCs with and without TrueCPR was: 112 (IQR 103-113) vs. 129 (IQR 122-135) compressions (p = 0.002). The degree of complete chest relaxation with the TrueCPR device was 95% (IQR 76-99) and without the device, 33% (IQR 29-38) (p < 0.001). In the simulation study performed, the use of the TrueCPR device resulted in a significant improvement in the quality of CCs in relation to frequency and depth of CCs and correctness of chest relaxation.

Sections du résumé

BACKGROUND
The aim of the study was to compare the quality of chest compressions (CCs) carried out with and without the use of the TrueCPR device during simulated cardiopulmonary resuscitations conducted by trainee doctors.
METHODS
The study was a prospective, randomized, cross-over simulation study. The study involved 65 trainee doctors who were tasked with performing a 2-min cycle of uninterrupted CCs under conditions of a simulated cardiopulmonary resuscitation of adults. CC were carried out in two scenarios: with and without TrueCPR chest compression support. Participants did not have experience in the use of CCs prior to this study.
RESULTS
The depth of compressions in regard to CC techniques were varied by 45 mm (IQR 43-48) for manual CC and 53 mm (IQR 51-55) for the TrueCPR device (p < 0.001). The incidence of CCs with and without TrueCPR was: 112 (IQR 103-113) vs. 129 (IQR 122-135) compressions (p = 0.002). The degree of complete chest relaxation with the TrueCPR device was 95% (IQR 76-99) and without the device, 33% (IQR 29-38) (p < 0.001).
CONCLUSIONS
In the simulation study performed, the use of the TrueCPR device resulted in a significant improvement in the quality of CCs in relation to frequency and depth of CCs and correctness of chest relaxation.

Identifiants

pubmed: 30155865
pii: VM/OJS/J/59295
doi: 10.5603/CJ.a2018.0091
pmc: PMC8084395
doi:

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

529-535

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Auteurs

Jolanta Majer (J)

Polish Society of Disaster Medicine, Warsaw, Poland.

Milosz J Jaguszewski (MJ)

I Department of Cardiology, Medical University of Gdansk, Poland.

Michael Frass (M)

Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Marcin Leskiewicz (M)

Department of Emergency Medical Service, Wroclaw Medical University, Wroclaw, Poland.

Jacek Smereka (J)

Department of Emergency Medical Service, Wroclaw Medical University, Wroclaw, Poland.

Jerzy R Ładny (JR)

Department of Emergency Medicine and Disaster, Medical University Bialystok, Bialystok, Poland.

Oliver Robak (O)

Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Łukasz Szarpak (Ł)

Lazarski University, Warsaw, Poland. lukasz.szarpak@gmail.com.

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