ST–Segment-Elevation Myocardial Infarction Patients Randomized to a Pharmaco-Invasive Strategy or Primary Percutaneous Coronary Intervention

医学 心肌梗塞 经皮冠状动脉介入治疗 内科学 心脏病学 ST段 心肌再灌注 随机对照试验
作者
Peter Sinnaeve,Paul W. Armstrong,Anthony Gershlick,Patrick Goldstein,Robert Wilcox,Yves Lambert,Thierry Danays,Louis Soulat,Sigrun Halvorsen,Fernando Rosell Ortiz,Katleen Vandenberghe,Anne Regelin,Erich Bluhmki,Kris Bogaerts,Frans Van de Werf
出处
期刊:Circulation [Lippincott Williams & Wilkins]
卷期号:130 (14): 1139-1145 被引量:89
标识
DOI:10.1161/circulationaha.114.009570
摘要

In the Strategic Reperfusion Early After Myocardial Infarction (STREAM) trial, a pharmaco-invasive (PI) strategy was compared with primary percutaneous coronary intervention (pPCI) in ST-segment-elevation myocardial infarction patients presenting within 3 hours after symptom onset but unable to undergo pPCI within 1 hour. At 30 days, the PI approach was associated with a nominally but nonstatistically significant lower incidence of the composite primary end point of death, shock, congestive heart failure, and reinfarction when compared with pPCI. The aim of the present study was to determine the effect of these strategies on 1-year mortality.Vital status at 1 year was available in 936 of 944 (99.2%) and 941 of 948 (99.3%) patients in the PI and pPCI arm, respectively. At 1 year, all-cause mortality rates (6.7% versus 5.9%) were similar for PI and pPCI-treated patients (P=0.49; risk ratio, 1.13; 95% confidence interval, 0.79-1.62). Cardiac mortality rates were similar as well (4.0% versus 4.1%, P=0.93; risk ratio, 0.98; 95% confidence interval, 0.62-1.54). Overall, only 34 patients died between day 30 and 1 year, 20 in the PI arm and 14 in the pPCI arm, of whom 20 died of noncardiac reasons (13 in the PI and 7 in the pPCI arm). There was no significant difference in 1-year all-cause mortality between the 2 groups among the prespecified key subgroups.At 1 year, mortality rates in the PI and pPCI arms were similar in ST-segment-elevation myocardial infarction patients presenting within 3 hours after symptom onset and unable to undergo pPCI within 1 hour.http://www.clinicaltrials.gov. Unique identifier: NCT00623623.
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