4.5 Article

Mechanical versus manual chest compressions in the treatment of in-hospital cardiac arrest patients in a non-shockable rhythm: A multi-centre feasibility randomised controlled trial (COMPRESS-RCT)

Journal

RESUSCITATION
Volume 158, Issue -, Pages 228-235

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.resuscitation.2020.09.033

Keywords

Cardiac arrest; Advanced life support; Cardiopulmonary resuscitation; Mechanical chest compressions; Randomised controlled trial; Feasibility trial

Funding

  1. NIHR [PDF 2015-08-109]
  2. NIHR Applied Research Centre (ARC) West Midlands, UK
  3. National Institutes of Health Research (NIHR) [PDF-2015-08-109] Funding Source: National Institutes of Health Research (NIHR)

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The study investigated the feasibility of using mechanical chest compression devices in adult in-hospital cardiac arrest patients through a randomized controlled trial. Results showed that while there were important factors limiting the progression to an effectiveness trial of mechanical CPR in the hospital setting, the findings will inform the design of future in-hospital intervention trials.
Background: Mechanical chest compression devices deliver high-quality chest compressions. Early data suggests that mechanical devices may be superior to manual chest compressions in adults following an in-hospital cardiac arrest patients. To determine the feasibility of undertaking an effectiveness trial in this population, we undertook a feasibility randomised controlled trial. Methods: We undertook a multi-centre parallel group feasibility randomised controlled trial (COMPRESS-RCT). Adult in-hospital cardiac arrest patients that were in a non-shockable rhythm were randomised in a 3:1 ratio to receive mechanical CPR (Jolfe AB/Stryker, Lund, Sweden) or ongoing manual CPR. Recruitment was led by the clinical cardiac arrest team. The primary study outcome was the proportion of eligible participants randomised in the study during site operational recruitment hours. Patients were enrolled under a model of deferred consent. We report data using descriptive statistics, point estimates and 95% confidence intervals. Results: Over a two-year period, we recruited 127 patients across five UK hospitals. We recruited 55.2% (95% CI 48.5%-61.8%) of eligible study participants in site operational recruitment hours. Most participantswere male (n = 76, 59.8%) with a mean age of 72 (95% CI: 69.9-74.9) years. Median arrest duration was 18 (IQR 13-29) minutes. In patients randomised to mech-CPR, median time from CPR start to device deployment was 11 (IQR 7 -15) minutes. ROSC was achieved in 27.6% (n = 35) participants and 4.7% (n = 6) were alive at 30-days. Conclusion: COMPRESS-RCT identified important factors that preclude progression to an effectiveness trial of mechanicalCPRin the hospital setting in the UK. Findings will inform the design of future in-hospital intra-arrest intervention trials. ISRCTN38139840, date of registration 9th January 2017.

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