Prasugrel compared with clopidogrel in patients undergoing percutaneous coronary intervention for ST-elevation myocardial infarction (TRITON-TIMI 38): double-blind, randomised controlled trial

被引:833
作者
Montalescot, Gilles [1 ]
Wiviott, Stephen D. [2 ]
Brounwald, Eugene [2 ]
Murphy, Sabina A. [2 ]
Gibson, C. Michael [2 ]
McCabe, Carolyn H. [2 ]
Antman, Elliott M. [2 ]
机构
[1] Univ Paris 06, Pitie Salpetriere Hosp, AP HP, INSERM,Inst Cardiol,U856, F-75013 Paris, France
[2] Brigham & Womens Hosp, Dept Med, Div Cardiol, TIMI Study Grp, Boston, MA 02115 USA
关键词
ORAL ANTIPLATELET THERAPY; PLATELET INHIBITION; STENT THROMBOSIS; UNCOATED STENTS; ASPIRIN; TICLOPIDINE; ABCIXIMAB; SAFETY; ANTICOAGULATION; THROMBOLYSIS;
D O I
10.1016/S0140-6736(09)60441-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Mechanical reperfusion with stenting for ST-elevation myocardial infarction (STEMI) is supported by dual antiplatelet treatment with aspirin and clopidogrel. Prasugrel, a potent and rapid-acting thienopyridine, is a potential alternative to clopidogrel. We aimed to assess prasugrel versus clopidogrel in patients undergoing percutaneous coronary intervention (PCI) for STEMI. Methods We under-took a double-blind, randomised controlled trial in 707 sites in 30 countries. 3534 participants presenting with STEMI were randomly assigned by interactive voice response system either prasugrel (60 mg loading, 10 mg maintenance [n=1769]) or clopidogrel (300 mg loading, 75 mg maintenance [n=1765]) and were unaware of the allocation. The primary endpoint was cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke. Efficacy analyses were by intention to treat. Follow-up was to 15 months, with secondary analyses at 30 days. This trial is registered with ClinicalTrials.gov, number NCT00097591. Findings At 30 days, 115 (6.5%) individuals assigned prasugrel had met the primary endpoint compared with 166 (9.5%) allocated clopidogrel (hazard ratio 0.68 [95% Cl 0.54-0.87]; p=0.0017). This effect continued to 15 months (174 [10.0%] vs 216 [12.4%]; 0.79 [0.65-0.97]; p=0.0221). The key secondary endpoint of cardiovascular death, myocardial infarction, or urgent target vessel revascularisation was also significantly reduced with prasugrel at 30 days (0.75 [0.59-0.96]; p=0.0205) and 15 months (0.79 [0.65-0.97]; p=0.0250), as was stent thrombosis. Treatments did not differ with respect to thrombolysis in myocardial infarction (TIMI) major bleeding unrelated to coronary-artery bypass graft (CABG) surgery at 30 days (p=0.3359) and 15 months (p=0.6451). TIMI life-threatening bleeding and TIMI major or minor bleeding were also similar with the two treatments, and only TIMI major bleeding after CABG surgery was significantly increased with prasugrel (p=0.0033). Interpretation In patients with STEMI undergoing PCI, prasugrel is more effective than clopidogrel for prevention of ischaemic events, without an apparent excess in bleeding.
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页码:723 / 731
页数:9
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