Targeted Temperature Management for 48 vs 24 Hours and Neurologic Outcome After Out-of-Hospital Cardiac Arrest

医学 目标温度管理 随机对照试验 重症监护室 不利影响 心理干预 复苏 自然循环恢复 重症监护 心肺复苏术 急诊医学 内科学 重症监护医学 精神科
作者
Hans Kirkegaard,Eldar Søreide,Inge de Haas,Ville Pettilä,Fabio Silvio Taccone,Urmet Arus,Christian Storm,Christian Hassager,Jørgen Feldbæk Nielsen,Christina Ankjær Sørensen,Susanne Ilkjær,Anni Nørgaard Jeppesen,Anders Morten Grejs,Christophe Henri Valdemar Duez,Jakob Hjort,Alf Inge Larsen,Valdo Toome,Marjaana Tiainen,Johanna Hästbacka,Timo Laitio
出处
期刊:JAMA [American Medical Association]
卷期号:318 (4): 341-341 被引量:294
标识
DOI:10.1001/jama.2017.8978
摘要

Importance

International resuscitation guidelines recommend targeted temperature management (TTM) at 33°C to 36°C in unconscious patients with out-of-hospital cardiac arrest for at least 24 hours, but the optimal duration of TTM is uncertain.

Objective

To determine whether TTM at 33°C for 48 hours results in better neurologic outcomes compared with currently recommended, standard, 24-hour TTM.

Design, Setting, and Participants

This was an international, investigator-initiated, blinded-outcome-assessor, parallel, pragmatic, multicenter, randomized clinical superiority trial in 10 intensive care units (ICUs) at 10 university hospitals in 6 European countries. Three hundred fifty-five adult, unconscious patients with out-of-hospital cardiac arrest were enrolled from February 16, 2013, to June 1, 2016, with final follow-up on December 27, 2016.

Interventions

Patients were randomized to TTM (33 ± 1°C) for 48 hours (n = 176) or 24 hours (n = 179), followed by gradual rewarming of 0.5°C per hour until reaching 37°C.

Main Outcomes and Measures

The primary outcome was 6-month neurologic outcome, with a Cerebral Performance Categories (CPC) score of 1 or 2 used to define favorable outcome. Secondary outcomes included 6-month mortality, including time to death, the occurrence of adverse events, and intensive care unit resource use.

Results

In 355 patients who were randomized (mean age, 60 years; 295 [83%] men), 351 (99%) completed the trial. Of these patients, 69% (120/175) in the 48-hour group had a favorable outcome at 6 months compared with 64% (112/176) in the 24-hour group (difference, 4.9%; 95% CI, −5% to 14.8%; relative risk [RR], 1.08; 95% CI, 0.93-1.25;P = .33). Six-month mortality was 27% (48/175) in the 48-hour group and 34% (60/177) in the 24-hour group (difference, −6.5%; 95% CI, −16.1% to 3.1%; RR, 0.81; 95% CI, 0.59-1.11;P = .19). There was no significant difference in the time to mortality between the 48-hour group and the 24-hour group (hazard ratio, 0.79; 95% CI, 0.54-1.15;P = .22). Adverse events were more common in the 48-hour group (97%) than in the 24-hour group (91%) (difference, 5.6%; 95% CI, 0.6%-10.6%; RR, 1.06; 95% CI, 1.01-1.12;P = .04). The median length of intensive care unit stay (151 vs 117 hours;P < .001), but not hospital stay (11 vs 12 days;P = .50), was longer in the 48-hour group than in the 24-hour group.

Conclusions and Relevance

In unconscious survivors from out-of-hospital cardiac arrest admitted to the ICU, targeted temperature management at 33°C for 48 hours did not significantly improve 6-month neurologic outcome compared with targeted temperature management at 33°C for 24 hours. However, the study may have had limited power to detect clinically important differences, and further research may be warranted.

Trial Registration

clinicaltrials.gov Identifier:NCT01689077
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