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Early intranasal medication administration in out-of-hospital cardiac arrest: a randomized simulation trial

dc.contributor.authorDowker, SR
dc.contributor.authorDowney, ML
dc.contributor.authorMajhail, NK
dc.contributor.authorScott, IG
dc.contributor.authorMathisson, J
dc.contributor.authorRizk, D
dc.contributor.authorTrumpower, B
dc.contributor.authorYake, D
dc.contributor.authorWilliams, M
dc.contributor.authorCoulter-Thompson, E
dc.contributor.authorBrent, CM
dc.contributor.authorSmith, Graham
dc.contributor.authorSwor, R
dc.contributor.authorRooney, Deborah
dc.contributor.authorNeumar, RW
dc.contributor.authorFriedman, CP
dc.contributor.authorCooke, JM
dc.contributor.authorMissel, AL
dc.coverage.spatialUnited States
dc.date.accessioned2024-08-01T18:47:08Z
dc.date.available2024-08-01T18:47:08Z
dc.date.issued2024-01-21
dc.identifier.issn2688-1152
dc.identifier.issn2688-1152
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pubmed/38260004
dc.identifier.urihttps://hdl.handle.net/2027.42/194151en
dc.description.abstractObjective: Intranasal 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. Methods: We 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. Results: Among 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%). Conclusions: INMA in LR resuscitation was associated with diminished resuscitation performance. INMA by FR did not impede key times or quality.
dc.format.mediumElectronic-eCollection
dc.languageeng
dc.publisherWiley
dc.rightsLicence for published version: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectOHCA
dc.subjectfirst responder
dc.subjectintranasal
dc.subjectlay rescuer
dc.subjectrandomized trial
dc.subjectsimulation
dc.titleEarly intranasal medication administration in out-of-hospital cardiac arrest: a randomized simulation trial
dc.typeArticle
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/194151/2/Early intranasal medication administration in out-of-hospital cardiac arrest Two randomized simulation trials.pdf
dc.identifier.doi10.1002/emp2.13100
dc.identifier.doihttps://dx.doi.org/10.7302/23595
dc.identifier.sourceJACEP Open
dc.description.versionPublished version
dc.date.updated2024-08-01T18:47:05Z
dc.identifier.orcid0000-0002-3280-7226
dc.identifier.orcid0000-0003-4560-2315
dc.identifier.orcid0000-0003-0577-2125
dc.identifier.orcid0000-0001-9335-4294
dc.identifier.orcid0000-0001-7942-8496
dc.identifier.orcid0000-0003-3395-5199
dc.identifier.orcid0000-0002-4761-7185
dc.identifier.orcid0000-0002-9879-0519
dc.description.filedescriptionDescription of Early intranasal medication administration in out-of-hospital cardiac arrest Two randomized simulation trials.pdf : Published version
dc.identifier.volume5
dc.identifier.issue1
dc.identifier.startpagee13100
dc.identifier.name-orcidDowker, SR
dc.identifier.name-orcidDowney, ML
dc.identifier.name-orcidMajhail, NK
dc.identifier.name-orcidScott, IG
dc.identifier.name-orcidMathisson, J
dc.identifier.name-orcidRizk, D
dc.identifier.name-orcidTrumpower, B
dc.identifier.name-orcidYake, D
dc.identifier.name-orcidWilliams, M
dc.identifier.name-orcidCoulter-Thompson, E; 0000-0002-3280-7226
dc.identifier.name-orcidBrent, CM; 0000-0003-4560-2315
dc.identifier.name-orcidSmith, Graham; 0000-0003-0577-2125
dc.identifier.name-orcidSwor, R
dc.identifier.name-orcidRooney, Deborah; 0000-0001-9335-4294
dc.identifier.name-orcidNeumar, RW; 0000-0001-7942-8496
dc.identifier.name-orcidFriedman, CP; 0000-0003-3395-5199
dc.identifier.name-orcidCooke, JM; 0000-0002-4761-7185
dc.identifier.name-orcidMissel, AL; 0000-0002-9879-0519
dc.working.doi10.7302/23595en
dc.owningcollnameLearning Health Sciences, Department of (DLHS)


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Licence for published version: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
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