Effect of Moderate vs Mild Therapeutic Hypothermia on Mortality and Neurologic Outcomes in Comatose Survivors of Out-of-Hospital Cardiac Arrest: The CAPITAL CHILL Randomized Clinical Trial.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
19 10 2021
Historique:
entrez: 19 10 2021
pubmed: 20 10 2021
medline: 28 10 2021
Statut: ppublish

Résumé

Comatose survivors of out-of-hospital cardiac arrest experience high rates of death and severe neurologic injury. Current guidelines recommend targeted temperature management at 32 °C to 36 °C for 24 hours. However, small studies suggest a potential benefit of targeting lower body temperatures. To determine whether moderate hypothermia (31 °C), compared with mild hypothermia (34 °C), improves clinical outcomes in comatose survivors of out-of-hospital cardiac arrest. Single-center, double-blind, randomized, clinical superiority trial carried out in a tertiary cardiac care center in eastern Ontario, Canada. A total of 389 patients with out-of-hospital cardiac arrest were enrolled between August 4, 2013, and March 20, 2020, with final follow-up on October 15, 2020. Patients were randomly assigned to temperature management with a target body temperature of 31 °C (n = 193) or 34 °C (n = 196) for a period of 24 hours. The primary outcome was all-cause mortality or poor neurologic outcome at 180 days. Neurologic outcome was assessed using the Disability Rating Scale, with poor neurologic outcome defined as a score greater than 5 (range, 0-29, with 29 being the worst outcome [vegetative state]). There were 19 secondary outcomes, including mortality at 180 days and length of stay in the intensive care unit. Among 367 patients included in the primary analysis (mean age, 61 years; 69 women [19%]), 366 (99.7%) completed the trial. The primary outcome occurred in 89 of 184 patients (48.4%) in the 31 °C group and in 83 of 183 patients (45.4%) in the 34 °C group (risk difference, 3.0% [95% CI, 7.2%-13.2%]; relative risk, 1.07 [95% CI, 0.86-1.33]; P = .56). Of the 19 secondary outcomes, 18 were not statistically significant. Mortality at 180 days was 43.5% and 41.0% in patients treated with a target temperature of 31 °C and 34 °C, respectively (P = .63). The median length of stay in the intensive care unit was longer in the 31 °C group (10 vs 7 days; P = .004). Among adverse events in the 31 °C group vs the 34 °C group, deep vein thrombosis occurred in 11.4% vs 10.9% and thrombus in the inferior vena cava occurred in 3.8% and 7.7%, respectively. In comatose survivors of out-of-hospital cardiac arrest, a target temperature of 31 °C did not significantly reduce the rate of death or poor neurologic outcome at 180 days compared with a target temperature of 34 °C. However, the study may have been underpowered to detect a clinically important difference. ClinicalTrials.gov Identifier: NCT02011568.

Identifiants

pubmed: 34665203
pii: 2785263
doi: 10.1001/jama.2021.15703
pmc: PMC8527358
doi:

Banques de données

ClinicalTrials.gov
['NCT02011568']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1494-1503

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Auteurs

Michel Le May (M)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Christina Osborne (C)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Juan Russo (J)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Derek So (D)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Aun Yeong Chong (AY)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Alexander Dick (A)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Michael Froeschl (M)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Christopher Glover (C)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Benjamin Hibbert (B)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Jean-François Marquis (JF)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Sophie De Roock (S)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Marino Labinaz (M)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Jordan Bernick (J)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Shawn Marshall (S)

University of Ottawa, The Ottawa Hospital, Ottawa, Ontario, Canada.

Ronnen Maze (R)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

George Wells (G)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.
School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.

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