P2Y12 receptor inhibitors for secondary prevention of ischemic stroke

被引:12
|
作者
Liu, Fang [1 ,2 ]
Tantry, Udaya S. [1 ]
Gurbel, Paul A. [1 ]
机构
[1] Sinai Ctr Thrombosis Res, Cardiac Catheterizat Lab, Baltimore, MD 21215 USA
[2] Beijing Hosp, Dept Neurol, Beijing, Peoples R China
基金
美国国家卫生研究院;
关键词
clopidogrel; P2Y(12) receptor inhibitor; prasugrel; stroke; ticagrelor; ticlopidine; ACUTE CORONARY SYNDROMES; DUAL ANTIPLATELET THERAPY; INTRACRANIAL ARTERIAL-STENOSIS; AGGRESSIVE MEDICAL THERAPY; ASSOCIATION TASK-FORCE; HIGH-RISK PATIENTS; CEREBRAL MICROBLEEDS; PLATELET INHIBITION; DOUBLE-BLIND; CARDIOVASCULAR ANGIOGRAPHY;
D O I
10.1517/14656566.2015.1035256
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Ischemic stroke ( IS) is a major cause of death and disability worldwide. The P2Y(12) receptor plays a critical role in the formation of a stable thrombus leading to ischemic complications. Therefore, P2Y(12) receptor inhibitors constitute a major antiplatelet strategy in the secondary prevention of IS. Areas covered: We searched articles about P2Y(12) receptor inhibitors and stroke in PubMed published until December 2014. This is a comprehensive review of the role of P2Y(12) receptor inhibitors alone and in combination with aspirin in the secondary prevention of noncardioembolic stroke. Expert opinion: The potential benefit of more potent antiplatelet therapy for secondary stroke prevention must be weighed against the risk of bleeding in patients with IS. Short-term (<= 3 months) dual antiplatelet therapy with clopidogrel and aspirin that is initiated early after IS or transient ischemic attack due to large artery atherosclerosis appears most efficient.
引用
收藏
页码:1149 / 1165
页数:17
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