Thrombolysis during Resuscitation for Out-of-Hospital Cardiac Arrest

被引:260
作者
Bottiger, Bernd W. [1 ,2 ]
Arntz, Hans-Richard [3 ]
Chamberlain, Douglas A. [4 ]
Bluhmki, Erich [5 ]
Belmans, Ann [6 ]
Danays, Thierry [7 ]
Carli, Pierre A. [8 ]
Adgey, Jennifer A. [9 ]
Bode, Christoph [10 ]
Wenzel, Volker [11 ]
机构
[1] Univ Cologne, Dept Anesthesiol & Postoperat Intens Care Med, D-50937 Cologne, Germany
[2] Heidelberg Univ, Heidelberg, Germany
[3] Benjamin Franklin Med Ctr, Charite, Berlin, Germany
[4] Cardiff Univ, Prehosp Emergency Res Unit, Sch Med, Cardiff, Wales
[5] Boehringer Ingelheim KG, Biberach, Germany
[6] Katholieke Univ Leuven, Ctr Biostat, Louvain, Belgium
[7] Boehringer Ingelheim KG, Reims, France
[8] Hop Necker Enfants Malad, Serv Aide Med Urgence Paris, Paris, France
[9] Royal Victoria Hosp, Reg Med Cardiol Ctr, Belfast BT12 6BA, Antrim, North Ireland
[10] Univ Freiburg, Freiburg, Germany
[11] Innsbruck Med Univ, Innsbruck, Austria
关键词
D O I
10.1056/NEJMoa070570
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Approximately 70% of persons who have an out-of-hospital cardiac arrest have underlying acute myocardial infarction or pulmonary embolism. Therefore, thrombolysis during cardiopulmonary resuscitation may improve survival. Methods: In a double-blind, multicenter trial, we randomly assigned adult patients with witnessed out-of-hospital cardiac arrest to receive tenecteplase or placebo during cardiopulmonary resuscitation. Adjunctive heparin or aspirin was not used. The primary end point was 30-day survival; the secondary end points were hospital admission, return of spontaneous circulation, 24-hour survival, survival to hospital discharge, and neurologic outcome. Results: After blinded review of data from the first 443 patients, the data and safety monitoring board recommended discontinuation of enrollment of asystolic patients because of low survival, and the protocol was amended. Subsequently, the trial was terminated prematurely for futility after enrolling a total of 1050 patients. Tenecteplase was administered to 525 patients and placebo to 525 patients; the two treatment groups had similar clinical profiles. We did not detect any significant differences between tenecteplase and placebo in the primary end point of 30-day survival (14.7% vs. 17.0%; P=0.36; relative risk, 0.87; 95% confidence interval, 0.65 to 1.15) or in the secondary end points of hospital admission (53.5% vs. 55.0%, P=0.67), return of spontaneous circulation (55.0% vs. 54.6%, P=0.96), 24-hour survival (30.6% vs. 33.3%, P=0.39), survival to hospital discharge (15.1% vs. 17.5%, P=0.33), or neurologic outcome (P=0.69). There were more intracranial hemorrhages in the tenecteplase group. Conclusions: When tenecteplase was used without adjunctive antithrombotic therapy during advanced life support for out-of-hospital cardiac arrest, we did not detect an improvement in outcome, in comparison with placebo. (ClinicalTrials.gov number, NCT00157261.).
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收藏
页码:2651 / 2662
页数:12
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