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dc.rights.licenseopenen_US
dc.contributor.authorLEVY, Bruno
dc.contributor.authorGIRERD, Nicolas
dc.contributor.authorAMOUR, Julien
dc.contributor.authorBESNIER, Emmanuel
dc.contributor.authorNESSELER, Nicolas
dc.contributor.authorHELMS, Julie
dc.contributor.authorDELMAS, Clément
dc.contributor.authorSONNEVILLE, Romain
dc.contributor.authorGUIDON, Catherine
dc.contributor.authorROZEC, Bertrand
dc.contributor.authorDAVID, Helène
dc.contributor.authorBOUGON, David
dc.contributor.authorCHAOUCH, Oussama
dc.contributor.authorWALID, Oulehri
dc.contributor.authorHERVÉ, Dupont
dc.contributor.authorBELIN, Nicolas
dc.contributor.authorGAIDE-CHEVRONNAY, Lucie
dc.contributor.authorROSSIGNOL, Patrick
dc.contributor.authorKIMMOUN, Antoine
dc.contributor.authorDUARTE, Kevin
dc.contributor.authorSLUTSKY, Arthur S
dc.contributor.authorBRODIE, Daniel
dc.contributor.authorFELLAHI, Jean-Luc
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorOUATTARA, Alexandre
dc.contributor.authorCOMBES, Alain
dc.date.accessioned2022-03-31T09:26:55Z
dc.date.available2022-03-31T09:26:55Z
dc.date.issued2022-02-01
dc.identifier.issn1538-3598en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/136579
dc.description.abstractEnThe optimal approach to the use of venoarterial extracorporeal membrane oxygenation (ECMO) during cardiogenic shock is uncertain. To determine whether early use of moderate hypothermia (33-34 °C) compared with strict normothermia (36-37 °C) improves mortality in patients with cardiogenic shock receiving venoarterial ECMO. Randomized clinical trial of patients (who were eligible if they had been endotracheally intubated and were receiving venoarterial ECMO for cardiogenic shock for <6 hours) conducted in the intensive care units at 20 French cardiac shock care centers between October 2016 and July 2019. Of 786 eligible patients, 374 were randomized. Final follow-up occurred in November 2019. Early moderate hypothermia (33-34 °C; n = 168) for 24 hours or strict normothermia (36-37 °C; n = 166). The primary outcome was mortality at 30 days. There were 31 secondary outcomes including mortality at days 7, 60, and 180; a composite outcome of death, heart transplant, escalation to left ventricular assist device implantation, or stroke at days 30, 60, and 180; and days without requiring a ventilator or kidney replacement therapy at days 30, 60, and 180. Adverse events included rates of severe bleeding, sepsis, and number of units of packed red blood cells transfused during venoarterial ECMO. Among the 374 patients who were randomized, 334 completed the trial (mean age, 58 [SD, 12] years; 24% women) and were included in the primary analysis. At 30 days, 71 patients (42%) in the moderate hypothermia group had died vs 84 patients (51%) in the normothermia group (adjusted odds ratio, 0.71 [95% CI, 0.45 to 1.13], P = .15; risk difference, -8.3% [95% CI, -16.3% to -0.3%]). For the composite outcome of death, heart transplant, escalation to left ventricular assist device implantation, or stroke at day 30, the adjusted odds ratio was 0.61 (95% CI, 0.39 to 0.96; P = .03) for the moderate hypothermia group compared with the normothermia group and the risk difference was -11.5% (95% CI, -23.2% to 0.2%). Of the 31 secondary outcomes, 30 were inconclusive. The incidence of moderate or severe bleeding was 41% in the moderate hypothermia group vs 42% in the normothermia group. The incidence of infections was 52% in both groups. The incidence of bacteremia was 20% in the moderate hypothermia group vs 30% in the normothermia group. In this randomized clinical trial involving patients with refractory cardiogenic shock treated with venoarterial ECMO, early application of moderate hypothermia for 24 hours did not significantly increase survival compared with normothermia. However, because the 95% CI was wide and included a potentially important effect size, these findings should be considered inconclusive. ClinicalTrials.gov Identifier: NCT02754193.
dc.language.isoENen_US
dc.subject.enBody Temperature
dc.subject.enConfidence Intervals
dc.subject.enErythrocyte Transfusion
dc.subject.enExtracorporeal Membrane Oxygenation
dc.subject.enFemale
dc.subject.enFrance
dc.subject.enHeart Transplantation
dc.subject.enHeart-Assist Devices
dc.subject.enHemorrhage
dc.subject.enHumans
dc.subject.enHypothermia
dc.subject.enInduced
dc.subject.enIntubation
dc.subject.enIntratracheal
dc.subject.enMale
dc.subject.enMiddle Aged
dc.subject.enRenal Replacement Therapy
dc.subject.enRespiration
dc.subject.enArtificial
dc.subject.enSepsis
dc.subject.enShock
dc.subject.enCardiogenic
dc.subject.enStroke
dc.subject.enTime Factors
dc.title.enEffect of Moderate Hypothermia vs Normothermia on 30-Day Mortality in Patients With Cardiogenic Shock Receiving Venoarterial Extracorporeal Membrane Oxygenation: A Randomized Clinical Trial.
dc.title.alternativeJAMAen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1001/jama.2021.24776en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed35103766en_US
bordeaux.journalJournal of the American Medical Associationen_US
bordeaux.page442-453en_US
bordeaux.volume327en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.issue5en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-03594058
hal.exportfalse
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
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