Aspirin and clopidogrel compared with clopidogrel alone after recent ischaemic stroke or transient ischaemic attack in high-risk patients (MATCH): randomised, double-blind, placebo-controlled trial

被引:1568
作者
Diener, HC
Bogousslavsky, J
Brass, LM
Cimminiello, C
Csiba, L
Kaste, M
Leys, D
Matias-Guiv, J
Rupprecht, HJ
机构
[1] Univ Essen Gesamthsch, Dept Neurol, D-45122 Essen, Germany
[2] CHU Vaudois, Dept Neurol, CH-1011 Lausanne, Switzerland
[3] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06510 USA
[4] Osped Vimercate, Div Med 2, Milan, Italy
[5] Univ Debrecen, Dept Neurol, Debrecen, Hungary
[6] Univ Helsinki, Dept Neurol, FIN-00014 Helsinki, Finland
[7] Univ Lille, Stroke Dept, Lille, France
[8] Hosp Gen Univ Alicante, Serv Neurol, Alicante, Spain
[9] Johannes Gutenberg Univ Mainz, Dept Med 2, D-6500 Mainz, Germany
关键词
D O I
10.1016/S0140-6736(04)16721-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Clopidogrel was superior to aspirin in patients with previous manifestations of atherothrombotic disease in the CAPRIE study and its benefit was amplified in some high-risk subgroups of patients. We aimed to assess whether addition of aspirin to clopidogrel could have a greater benefit than clopidogrel alone in prevention of vascular events with potentially higher bleeding risk. Methods We did a randomised, double-blind, placebo-controlled trial to compare aspirin (75 mg/day) with placebo in 7599 high-risk patients with recent ischaemic stroke or transient ischaemic attack and at least one additional vascular risk factor who were already receiving clopidogrel 75 mg/day. Duration of treatment and follow-up was 18 months. The primary endpoint was a composite of ischaemic stroke, myocardial infarction, vascular death, or rehospitalisation for acute ischaemia (including rehospitalisation for transient ischaemic attack, angina pectoris, or worsening of peripheral arterial disease). Analysis was by intention to treat, using logrank test and a Cox's proportional-hazards model. Findings 596 (15.7%) patients reached the primary endpoint in the group receiving aspirin and clopidogrel compared with 636 (16.7%) in the clopidogrel alone group (relative risk reduction 6.4%, [95% CI-4.6 to 16.3]; absolute risk reduction 1% [0.6 to 2.7]). Life-threatening bleedings were higher in the group receiving aspirin and clopidogrel versus clopidogrel alone (96 [2.6%] vs 49 [1.3%]; absolute risk increase 1.3% [95% CI 0.6 to 1.9]). Major bleedings were also increased in the group receiving aspirin and clopidogrel but no difference was recorded in mortality. Interpretation Adding aspirin to clopidogrel in high-risk patients with recent ischaemic stroke or transient ischaemic attack is associated with a non-significant difference in reducing major vascular events. However, the risk of life-threatening or major bleeding is increased by the addition of aspirin.
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页码:331 / 337
页数:7
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