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Randomised controlled trial of simulation-based education for mechanical cardiopulmonary resuscitation training.
Coggins, Andrew R; Nottingham, Cameron; Byth, Karen; Ho, Kevin R; Aulia, Felicia A; Murphy, Margaret; Shetty, Amith L; Todd, Anna; Moore, Nathan.
Affiliation
  • Coggins AR; Emergency Department, Westmead Hospital, Sydney, New South Wales, Australia.
  • Nottingham C; Western Clinical School, University of Sydney, Sydney, New South Wales, Australia.
  • Byth K; Western Clinical School, University of Sydney, Sydney, New South Wales, Australia.
  • Ho KR; Western Clinical School, University of Sydney, Sydney, New South Wales, Australia.
  • Aulia FA; Western Clinical School, University of Sydney, Sydney, New South Wales, Australia.
  • Murphy M; Emergency Department, Westmead Hospital, Sydney, New South Wales, Australia.
  • Shetty AL; Emergency Department, Westmead Hospital, Sydney, New South Wales, Australia.
  • Todd A; Emergency Department, Westmead Hospital, Sydney, New South Wales, Australia.
  • Moore N; Western Clinical School, University of Sydney, Sydney, New South Wales, Australia.
Emerg Med J ; 36(5): 266-272, 2019 May.
Article in En | MEDLINE | ID: mdl-31015214
ABSTRACT

INTRODUCTION:

Mechanical cardiopulmonary resuscitation (M-CPR) is increasingly used in the management of cardiac arrest. There are no previously reported randomised studies investigating M-CPR training. This study of newly trained M-CPR providers hypothesised that a brief simulation-based intervention after 4 months would improve M-CPR performance at 6 months.

METHODS:

This study used a simulated 'in situ' cardiac arrest model. The M-CPR device used was a proprietary Lund University Cardiac Assist System 3 machine (Physio Control, Redmond, Washington, USA). Standardised baseline training was provided to all participants. Following training, baseline performance was assessed. The primary outcome measure was the time taken to initiate M-CPR and the secondary outcome was performance against a checklist of errors. Participants were then randomised to intervention group (simulation training) or control group (routine clinical use of M-CPR). After 6 months the outcome measures were reassessed. Comparative statistical tests used an intention-to-treat analysis.

RESULTS:

112 participants were enrolled. The intervention group (n=60) and control group (n=52) had similar demographic characteristics. At the 6-month assessment, median time to M-CPR initiation was 27.0 s (IQR 22.0-31.0) in the intervention group and 31.0 s (IQR 25.6-46.0) in the control group (p=0.003). The intervention group demonstrated fewer errors compared with controls at 6 months (p<0.001)

CONCLUSION:

In this randomised study of approaches to M-CPR training, providers receiving additional simulation-based training had higher retention levels of M-CPR skills. Therefore, when resuscitation skills are newly learnt, provision follow-up training should be an important consideration.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiopulmonary Resuscitation / Simulation Training Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: America do norte Language: En Journal: Emerg Med J Journal subject: MEDICINA DE EMERGENCIA Year: 2019 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiopulmonary Resuscitation / Simulation Training Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: America do norte Language: En Journal: Emerg Med J Journal subject: MEDICINA DE EMERGENCIA Year: 2019 Type: Article Affiliation country: Australia