Advances in Antiplatelet Therapy: Agents in Clinical Development

被引:74
|
作者
Angiolillo, Dominick J. [1 ]
Bhatt, Deepak L. [2 ]
Gurbel, Paul A. [3 ]
Jennings, Lisa K. [4 ,5 ,6 ,7 ]
机构
[1] Univ Florida, Coll Med Jacksonville, Div Cardiol, Jacksonville, FL 32209 USA
[2] Brigham & Womens Hosp, Vet Affairs Boston Healthcare Syst, Boston, MA 02115 USA
[3] Johns Hopkins Univ, Sch Med, Cardiac Catheterizat Lab, Sinai Hosp Baltimore,Sinai Ctr Thrombosis Res, Baltimore, MD USA
[4] Univ Memphis, Vasc Biol Ctr Excellence, Dept Internal Med, Memphis, TN 38152 USA
[5] Univ Memphis, Vasc Biol Ctr Excellence, Dept Mol Sci & Surg, Memphis, TN 38152 USA
[6] Univ Memphis, Vasc Biol Ctr Excellence, Dept Biomed Engn, Memphis, TN 38152 USA
[7] Univ Tennessee, Ctr Hlth Sci, Cardiovasc Clin Res Consortium, TAM, Memphis, TN 38163 USA
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2009年 / 103卷 / 3A期
基金
美国国家卫生研究院;
关键词
ACUTE CORONARY SYNDROMES; PROTEASE-ACTIVATED RECEPTORS; HUMAN PLATELET ACTIVATION; PRASUGREL ACHIEVES GREATER; ASPIRIN-TREATED PATIENTS; ST-SEGMENT ELEVATION; P2Y(12) RECEPTOR; PROCOAGULANT ACTIVITY; EFFICIENT GENERATION; ARTERY-DISEASE;
D O I
10.1016/j.amjcard.2008.11.023
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Antiplatelet agents are the cornerstone of treatment for patients with acute coronary syndromes and patients undergoing percutaneous coronary intervention. The current "gold standard" consists of a combination of aspirin and clopidogrel administered orally shortly before invasive procedures and then continued in the form of maintenance doses. Not all patients respond optimally to standard therapy. Resistance to the antiplatelet activity of both drugs when used either singly or in combination has been observed and may lead to treatment failure, including further atherothrombotic events. Potential limitations associated with the combined use of aspirin and clopidogrel have inspired clinical investigation into several promising new antiplatelet agents as potential additions or alternatives to standard therapy. The candidates include prasugrel, which has a mechanism similar to that of clopidogrel but with superior pharmacokinetics; ticagrelor, a nonthienopyridine that binds reversibly to the platelet P2Y(12) receptor; cangrelor, an intravenously administered analogue of ticagrelor; and various thrombin receptor antagonists. (C) 2009 Published by Elsevier Inc. (Am J Cardiol 2009;103[suppl]:40A-51A)
引用
收藏
页码:40A / 51A
页数:12
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