Hypothermia versus Normothermia after Out-of-Hospital Cardiac Arrest

Josef Dankiewicz(Lund University), Tobias Cronberg(Lund University), Gisela Lilja(Lund University), Janus Christian Jakobsen(University of Copenhagen), Helena Levin(Lund University), Susann Ullén(Lund University), Christian Rylander(University of Gothenburg), Matt P. Wise(University Hospital of Wales), Mauro Oddo(University Hospital of Lausanne), Alain Cariou(Délégation Paris 5), Jan Bělohlávek(Charles University), Jan Hovdenes(Oslo University Hospital), Manoj Saxena(Bankstown Lidcombe Hospital), Hans Kirkegaard(Aarhus University Hospital), Paul J. Young(Wellington Hospital), Paolo Pelosi(Ospedale Policlinico San Martino), Christian Storm(Charité - Universitätsmedizin Berlin), Fabio Silvio Taccone(Université Libre de Bruxelles), Michael Joannidis(Innsbruck Medical University), Clifton W. Callaway(University of Pittsburgh), Glenn M. Eastwood(Australian and New Zealand Intensive Care Society), Matt Morgan(University Hospital of Wales), Per Nordberg(Karolinska Institutet), David Erlinge(Lund University), Alistair Nichol(University College Dublin), Michelle S. Chew(Linköping University), Jacob Hollenberg(Karolinska Institutet), Matthew Thomas(Bristol Royal Infirmary), Jeremy Bewley(Bristol Royal Infirmary), Katie Sweet(Bristol Royal Infirmary), Anders Morten Grejs(Aarhus University Hospital), Steffen Christensen(Aarhus University Hospital), Matthias Hænggi(University of Bern), Anja Levis(University of Bern), Andreas Lundin(University of Gothenburg), Joachim Düring(Skåne University Hospital), Simon Schmidbauer(Skåne University Hospital), Thomas Keeble(Essex Cardiothoracic Centre), Grigoris V. Karamasis(Essex Cardiothoracic Centre), Claudia Schrag(University of Bern), Edith Faessler(University of Bern), Ondřej Šmíd(Charles University), Michal Otáhal(Charles University), Marco Maggiorini(University Hospital of Zurich), Pedro David Wendel‐Garcia(University Hospital of Zurich), Paul Jaubert(Délégation Paris 5), Jade Cole(University Hospital of Wales), Miroslav Solař(Charles University), Ola Borgquist(Lund University), Christoph Leithner(Charité - Universitätsmedizin Berlin), Samia Abed‐Maillard(University Hospital of Lausanne), Leanlove Navarra(Wellington Hospital), Martin Annborn(Lund University), Johan Undén(Lund University), Iole Brunetti(Ospedale Policlinico San Martino), Akil Awad(Karolinska Institutet), Peter McGuigan(University of Ulster), Roy Bjørkholt Olsen(Sørlandet Hospital Arendal), Tiziano Cassina(Epatocentro Ticino), Philippe Vignon(Hôpital Dupuytren), Halvor Langeland(Norwegian University of Science and Technology), Theis Lange(University of Copenhagen), Hans Friberg(Skåne University Hospital), Niklas Nielsen(Lund University)
New England Journal of Medicine
June 16, 2021
Cited by 972Open Access
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Abstract

BACKGROUND: Targeted temperature management is recommended for patients after cardiac arrest, but the supporting evidence is of low certainty. METHODS: In an open-label trial with blinded assessment of outcomes, we randomly assigned 1900 adults with coma who had had an out-of-hospital cardiac arrest of presumed cardiac or unknown cause to undergo targeted hypothermia at 33°C, followed by controlled rewarming, or targeted normothermia with early treatment of fever (body temperature, ≥37.8°C). The primary outcome was death from any cause at 6 months. Secondary outcomes included functional outcome at 6 months as assessed with the modified Rankin scale. Prespecified subgroups were defined according to sex, age, initial cardiac rhythm, time to return of spontaneous circulation, and presence or absence of shock on admission. Prespecified adverse events were pneumonia, sepsis, bleeding, arrhythmia resulting in hemodynamic compromise, and skin complications related to the temperature management device. RESULTS: A total of 1850 patients were evaluated for the primary outcome. At 6 months, 465 of 925 patients (50%) in the hypothermia group had died, as compared with 446 of 925 (48%) in the normothermia group (relative risk with hypothermia, 1.04; 95% confidence interval [CI], 0.94 to 1.14; P = 0.37). Of the 1747 patients in whom the functional outcome was assessed, 488 of 881 (55%) in the hypothermia group had moderately severe disability or worse (modified Rankin scale score ≥4), as compared with 479 of 866 (55%) in the normothermia group (relative risk with hypothermia, 1.00; 95% CI, 0.92 to 1.09). Outcomes were consistent in the prespecified subgroups. Arrhythmia resulting in hemodynamic compromise was more common in the hypothermia group than in the normothermia group (24% vs. 17%, P<0.001). The incidence of other adverse events did not differ significantly between the two groups. CONCLUSIONS: In patients with coma after out-of-hospital cardiac arrest, targeted hypothermia did not lead to a lower incidence of death by 6 months than targeted normothermia. (Funded by the Swedish Research Council and others; TTM2 ClinicalTrials.gov number, NCT02908308.).


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