1. Thrombolysis during Resuscitation for Out-of-Hospital Cardiac Arrest
- Author
-
Böttiger, B, Arntz, H, Chamberlain, D, Bluhmki, E, Belmans, A, Danays, T, Carli, P, Adgey, J, Bode, C, Wenzel, V, in TROICA Trial Investigators, the European Resuscitation Council Study Group, PESENTI, ANTONIO MARIA, Böttiger, B, Arntz, H, Chamberlain, D, Bluhmki, E, Belmans, A, Danays, T, Carli, P, Adgey, J, Bode, C, Wenzel, V, Pesenti, A, in TROICA Trial, I, and the European Resuscitation Council Study, G
- Subjects
Male ,medicine.medical_specialty ,Resuscitation ,medicine.medical_treatment ,Tenecteplase ,Kaplan-Meier Estimate ,Return of spontaneous circulation ,Follow-Up Studie ,Double-Blind Method ,Multicenter trial ,medicine ,Thrombolytic Therapy ,Treatment Failure ,Myocardial infarction ,Cardiopulmonary resuscitation ,Survival rate ,Aged ,Intracranial Hemorrhage ,Chi-Square Distribution ,Fibrinolytic Agent ,business.industry ,General Medicine ,Middle Aged ,medicine.disease ,Cardiopulmonary Resuscitation ,Heart Arrest ,Advanced life support ,Surgery ,Survival Rate ,Prospective Studie ,Tissue Plasminogen Activator ,Anesthesia ,Female ,business ,Human ,medicine.drug - Abstract
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. Tenec teplase 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 tenecte plase 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.)
- Published
- 2008