Early intranasal medication administration in out‐of‐hospital cardiac arrest: Two randomized simulation trials

Author:

Dowker Stephen R.1,Downey Madison L.1,Majhail Noor K.1,Scott Isabella G.1,Mathisson Jonah1,Rizk Daniel1,Trumpower Brad2,Yake Debra1,Williams Michelle1,Coulter‐Thompson Emilee I.13,Brent Christine M.4,Smith Graham C.4,Swor Robert56,Berger David A.56,Rooney Deborah M.1,Neumar Robert W.47,Friedman Charles P.1,Cooke James M.18,Missel Amanda L.1ORCID

Affiliation:

1. Department of Learning Health Sciences University of Michigan Medical School Ann Arbor Michigan USA

2. Department of Internal Medicine Division of Cardiovascular Medicine University of Michigan Medical School, 2139 Cardiovascular Center Ann Arbor Michigan USA

3. Center for Bioethics and Social Sciences in Medicine, University of Michigan Ann Arbor Michigan USA

4. Department of Emergency Medicine University of Michigan Medical School Ann Arbor Michigan USA

5. Department of Emergency Medicine Corewell East William Beaumont University Hospital Royal Oak Michigan USA

6. Department of Emergency Medicine Oakland University William Beaumont School of Medicine Rochester Michigan USA

7. Max Harry Weil Institute for Critical Care Research and Innovation, University of Michigan Ann Arbor Michigan USA

8. Department of Family Medicine University of Michigan Medical School Ann Arbor Michigan USA

Abstract

AbstractObjectiveIntranasal medications have been proposed as adjuncts to out‐of‐hospital cardiac arrest (OHCA) care. We sought to quantify the effects of intranasal medication administration (INMA) in OHCA workflows.MethodsWe conducted separate randomized OHCA simulation trials with lay rescuers (LRs) and first responders (FRs). Participants were randomized to groups performing hands‐only cardiopulmonary resuscitation (CPR)/automated external defibrillator with or without INMA during the second analysis phase. Time to compression following the second shock (CPR2) was the primary outcome and compression quality (chest compression rate (CCR) and fraction (CCF)) was the secondary outcome. We fit linear regression models adjusted for CPR training in the LR group and service years in the FR group.ResultsAmong LRs, INMA was associated with a significant increase in CPR2 (mean diff. 44.1 s, 95% CI: 14.9, 73.3), which persisted after adjustment (p = 0.005). We observed a significant decrease in CCR (INMA 95.1 compressions per min (cpm) vs control 104.2 cpm, mean diff. −9.1 cpm, 95% CI −16.6, −1.6) and CCF (INMA 62.4% vs control 69.8%, mean diff. −7.5%, 95% CI −12.0, −2.9). Among FRs, we found no significant CPR2 delays (mean diff. −2.1 s, 95% CI −15.9, 11.7), which persisted after adjustment (p = 0.704), or difference in quality (CCR INMA 115.5 cpm vs control 120.8 cpm, mean diff. −5.3 cpm, 95% CI −12.6, 2.0; CCF INMA 79.6% vs control 81.2% mean diff. −1.6%, 95% CI −7.4, 4.3%)ConclusionsINMA in LR resuscitation was associated with diminished resuscitation performance. INMA by FR did not impede key times or quality.

Funder

American Heart Association

National Institutes of Health

Publisher

Wiley

Reference19 articles.

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