New P2Y12 Inhibitors Versus Clopidogrel in Percutaneous Coronary Intervention: A Meta-Analysis

被引:95
作者
Bellemain-Appaix, Anne [1 ]
Brieger, David [1 ]
Beygui, Farzin [1 ]
Silvain, Johanne [1 ]
Pena, Ana [1 ]
Cayla, Guillaume [1 ]
Barthelemy, Olivier [1 ]
Collet, Jean-Philippe [1 ]
Montalescot, Gilles [1 ]
机构
[1] Pitie Salpetriere Univ Hosp, AP HP, Inst Cardiol, Paris, France
关键词
acute coronary syndrome; cangrelor; clopidogrel; elinogrel; P2Y(12) antagonists; percutaneous coronary intervention; prasugrel; ELEVATION MYOCARDIAL-INFARCTION; RANDOMIZED CONTROLLED-TRIAL; DOUBLE-BLIND; CARDIOVASCULAR EVENTS; ANTIPLATELET THERAPY; PLATELET INHIBITION; RECEPTOR ANTAGONIST; PRASUGREL; PCI; ASPIRIN;
D O I
10.1016/j.jacc.2010.07.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The purpose of this study was to perform a meta-analysis of randomized trials that compare new P2Y(12) inhibitors with clopidogrel to determine whether they improve clinical outcomes after percutaneous intervention (PCI). Background Ticlopidine/clopidogrel prevents major adverse cardiac events after PCI, but no trials have shown an effect on mortality. New P2Y(12) inhibitors are more potent and evaluated in PCI. Whether they decrease mortality after PCI compared with clopidogrel is unknown. Methods MEDLINE and Cochrane Controlled Trials Register databases were searched from January 1980 through January 2010. Randomized, placebo-controlled trials that compared new P2Y(12) antagonists with clopidogrel in PCI were selected. Data from 8 studies were evaluated and analyses performed for all randomized patients, PCI patients (any PCI), and PCI for ST-segment elevation myocardial infarction (STEMI) patients. All-cause mortality was the primary efficacy end point. Thrombolysis In Myocardial Infarction major bleeding was the primary safety end point. Results A total of 48,599 patients were included with 94% of patients with acute coronary syndrome and 84% of patients undergoing PCI. New P2Y(12) inhibitors significantly decreased death (odds ratio [OR]: 0.83, 95% confidence interval [CI]: 0.75 to 0.92, p < 0.001 for the whole cohort; OR: 0.85, 95% CI: 0.75 to 0.96, p = 0.008 for any PCI; and OR: 0.78, 95% CI: 0.66 to 0.92, p = 0.003 for PCI for STEMI). In PCI patients, new P2Y(12) inhibitors also significantly decreased major adverse cardiac events by 18% (p < 0.001) and stent thrombosis by 40% (p < 0.001). Although there was an increase in Thrombolysis In Myocardial Infarction major bleeding for any PCI (OR: 1.23, 95% CI: 1.04 to 1.46, p = 0.01), no difference was observed in PCI for STEMI (OR: 0.98, 95% CI: 0.85 to 1.13, p = 0.76), with similar outcomes in primary PCI for STEMI. Results were confirmed in sensitivity analyses that removed the largest study. Conclusions New P2Y(12) inhibitors decrease mortality after PCI compared with clopidogrel. The risk/benefit ratio is particularly favorable in PCI for STEMI patients. (J Am Coll Cardiol 2010;56:1542-51) (C) 2010 by the American College of Cardiology Foundation
引用
收藏
页码:1542 / 1551
页数:10
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