Effect of Trans-Nasal Evaporative Intra-arrest Cooling on Functional Neurologic Outcome in Out-of-Hospital Cardiac Arrest: The PRINCESS Randomized Clinical Trial

IMPORTANCE: Therapeutic hypothermia may increase survival with good neurologic outcome after cardiac arrest. Trans-nasal evaporative cooling is a method used to induce cooling, primarily of the brain, during cardiopulmonary resuscitation (ie, intra-arrest). OBJECTIVE: To determine whether prehospita...

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Veröffentlicht in:JAMA : the journal of the American Medical Association 2019-05, Vol.321 (17), p.1677-1685
Hauptverfasser: Nordberg, Per, Taccone, Fabio Silvio, Truhlar, Anatolij, Forsberg, Sune, Hollenberg, Jacob, Jonsson, Martin, Cuny, Jerome, Goldstein, Patrick, Vermeersch, Nick, Higuet, Adeline, Jiménes, Francisco Carmona, Ortiz, Fernando Rosell, Williams, Julia, Desruelles, Didier, Creteur, Jacques, Dillenbeck, Emelie, Busche, Caroline, Busch, Hans-Jörg, Ringh, Mattias, Konrad, David, Peterson, Johan, Vincent, Jean-Louis, Svensson, Leif
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Sprache:eng
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Zusammenfassung:IMPORTANCE: Therapeutic hypothermia may increase survival with good neurologic outcome after cardiac arrest. Trans-nasal evaporative cooling is a method used to induce cooling, primarily of the brain, during cardiopulmonary resuscitation (ie, intra-arrest). OBJECTIVE: To determine whether prehospital trans-nasal evaporative intra-arrest cooling improves survival with good neurologic outcome compared with cooling initiated after hospital arrival. DESIGN, SETTING, AND PARTICIPANTS: The PRINCESS trial was an investigator-initiated, randomized, clinical, international multicenter study with blinded assessment of the outcome, performed by emergency medical services in 7 European countries from July 2010 to January 2018, with final follow-up on April 29, 2018. In total, 677 patients with bystander-witnessed out-of-hospital cardiac arrest were enrolled. INTERVENTIONS: Patients were randomly assigned to receive trans-nasal evaporative intra-arrest cooling (n = 343) or standard care (n = 334). Patients admitted to the hospital in both groups received systemic therapeutic hypothermia at 32°C to 34°C for 24 hours. MAIN OUTCOMES AND MEASURES: The primary outcome was survival with good neurologic outcome, defined as Cerebral Performance Category (CPC) 1-2, at 90 days. Secondary outcomes were survival at 90 days and time to reach core body temperature less than 34°C. RESULTS: Among the 677 randomized patients (median age, 65 years; 172 [25%] women), 671 completed the trial. Median time to core temperature less than 34°C was 105 minutes in the intervention group vs 182 minutes in the control group (P 
ISSN:0098-7484
1538-3598
DOI:10.1001/jama.2019.4149