Targeted temperature management at 33°C versus 36°C after cardiac arrest.
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Nielsen Niklas, Wetterslev Jørn, Cronberg Tobias, Erlinge David, Gasche Yvan, Hassager Christian, Horn Janneke, Hovdenes Jan, Kjaergaard Jesper, Kuiper Michael, Pellis Tommaso, Stammet Pascal, Wanscher Michael, Wise Matt P, Åneman Anders, Al-Subaie Nawaf, Boesgaard Søren, Bro-Jeppesen John, Brunetti Iole, Bugge Jan Frederik, Hingston Christopher D, Juffermans Nicole P, Koopmans Matty, Køber Lars, Langørgen Jørund, Lilja Gisela, Møller Jacob Eifer, Rundgren Malin, Rylander Christian, Smid Ondrej, Werer Christophe, Winkel Per, Friberg Hans, TTM Trial Investigators
Аннотация
METHODS: In an international trial, we randomly assigned 950 unconscious adults after out-of-hospital cardiac arrest of presumed cardiac cause to targeted temperature management at either 33°C or 36°C. The primary outcome was all-cause mortality through the end of the trial. Secondary outcomes included a composite of poor neurologic function or death at 180 days, as evaluated with the Cerebral Performance Category (CPC) scale and the modified Rankin scale.
RESULTS: In total, 939 patients were included in the primary analysis. At the end of the trial, 50% of the patients in the 33°C group (235 of 473 patients) had died, as compared with 48% of the patients in the 36°C group (225 of 466 patients) (hazard ratio with a temperature of 33°C, 1.06; 95% confidence interval [CI], 0.89 to 1.28; P=0.51). At the 180-day follow-up, 54% of the patients in the 33°C group had died or had poor neurologic function according to the CPC, as compared with 52% of patients in the 36°C group (risk ratio, 1.02; 95% CI, 0.88 to 1.16; P=0.78). In the analysis using the modified Rankin scale, the comparable rate was 52% in both groups (risk ratio, 1.01; 95% CI, 0.89 to 1.14; P=0.87). The results of analyses adjusted for known prognostic factors were similar.
CONCLUSIONS: In unconscious survivors of out-of-hospital cardiac arrest of presumed cardiac cause, hypothermia at a targeted temperature of 33°C did not confer a benefit as compared with a targeted temperature of 36°C. (Funded by the Swedish Heart-Lung Foundation and others; TTM ClinicalTrials.gov number, NCT01020916.).