Prasugrel: A Novel Platelet ADP P2Y12 Receptor Antagonist

被引:6
作者
Wilson, William [1 ]
Gurvitch, Ronen [1 ]
Ajani, Andrew E. [1 ,2 ,3 ]
机构
[1] Royal Melbourne Hosp, Dept Cardiol, Parkville, Vic 3050, Australia
[2] Monash Univ, NHMRC Ctr Clin Res Excellence Therapeut, Dept Epidemiol & Prevent Med, Melbourne, Vic 3004, Australia
[3] Univ Melbourne, Melbourne, Vic, Australia
关键词
Prasugrel; Acute coronary syndrome; Percutaneous coronary intervention; PERCUTANEOUS CORONARY INTERVENTION; ORAL ANTIPLATELET THERAPY; ST-SEGMENT ELEVATION; MYOCARDIAL-INFARCTION; DOSE CLOPIDOGREL; CONTROLLED TRIAL; ARTERY-DISEASE; ASPIRIN; PRETREATMENT; AGGREGATION;
D O I
10.1111/j.1755-5922.2009.00086.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The antiplatelet drug prasugrel is one of the new generations of thienopyridines, drugs that inhibit the platelet P2Y(12) receptor. It is becoming clear that there is variability in individual responses to antiplatelet agents such as clopidogrel, which may limit their efficacy and widespread utility. A number of controversies remain, such as varied definitions of "nonresponders" to antiplatelet therapy, the optimal means of assessing platelet function, and the potential capacity of in vivo platelet function studies to predict future clinical events. Prasugrel provides more rapid and consistent platelet inhibition than does clopidogrel, yet its clinical utility is under scrutiny. We aim to review the available data evaluating the efficacy and safety of this novel antiplatelet agent.
引用
收藏
页码:194 / 198
页数:5
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