Antiplatelet therapy: Resistance to traditional antiaggregation drugs and role of new antiplatelet agents

被引:1
作者
del Castillo-Carnevali, Hugo [1 ]
Barrios Alonso, Vivencio [1 ]
Zamorano Gomez, Jose Luis [1 ]
机构
[1] Hosp Univ Ramon y Cajal, Serv Cardiol, Madrid, Spain
来源
MEDICINA CLINICA | 2014年 / 143卷 / 05期
关键词
Aspirin; Clopidogrel; Genetics; Individualization; Risk factors; Resistance; Guidelines; Prasugrel; Ticagrelor; PERCUTANEOUS CORONARY INTERVENTION; LOW-DOSE ASPIRIN; ACUTE MYOCARDIAL-INFARCTION; PLATELET REACTIVITY; CARDIOVASCULAR-DISEASE; PRIMARY PREVENTION; HEART-FAILURE; CLOPIDOGREL; RISK; POLYMORPHISMS;
D O I
10.1016/j.medcli.2013.09.034
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Platelet aggregation plays a key role in the development of major cardiovascular events (MACE) related to atherothrombosis. Since the appearance of coronary stenting, the importance of measuring and modulating platelet activity has considerably increased in the scientific literature during the last decade. Double antiplatelet therapy with aspirin and clopidogrel administrated to stent carriers has widely demonstrated its efficacy in the prevention of MACE compared with aspirin alone. These benefits are also present when a conservatory approach is chosen for acute coronary syndrome management. However, there are an important number of patients who develop MACE despite optimal dual antiplatelet therapy, most likely related to an incomplete platelet activity inhibition. Many studies suggest an important inter-individual variability in the response to the drugs, maybe related, at least in part, to the use of different assessment techniques of platelet aggregation. Other authors suggest an incomplete platelet inhibition as a possible explanation for the presence of MACE in patients under optimal antiplatelet therapy. Resistance to usual drugs has become a clinically relevant issue that requires an individual approach where new antiplatelet agents, such as prasugrel or ticagrelor, could play an important role as stated in current consensus documents. (C) 2013 Elsevier Espana, S.L. All rights reserved.
引用
收藏
页码:222 / 229
页数:8
相关论文
共 59 条
[1]  
[Anonymous], BMJ
[2]  
[Anonymous], N ENGL J MED
[3]  
[Anonymous], 2001, COCHRANE DB SYST REV
[4]  
[Anonymous], COCHRANE DATABASE SY
[5]   ISIS-2: 10 year survival among patients with suspected acute myocardial infarction in randomised comparison of intravenous streptokinase, oral aspirin, both, or neither [J].
Baigent, C ;
Collins, R ;
Appleby, P ;
Parish, S ;
Sleight, P ;
Peto, R .
BMJ-BRITISH MEDICAL JOURNAL, 1998, 316 (7141) :1337-1343
[6]   Acetylation of prostaglandnin H2 synthases by aspirin is inhibited by redox cycling of the peroxidase [J].
Bala, Manju ;
Chin, Cindy N. ;
Logan, Asha T. ;
Amin, Taneem ;
Marnett, Lawrence J. ;
Boutaud, Olivier ;
Oates, John A. .
BIOCHEMICAL PHARMACOLOGY, 2008, 75 (07) :1472-1481
[7]   A systematic review and meta-analysis on the hazards of discontinuing or not adhering to aspirin among 50 279 patients at risk for coronary artery disease [J].
Biondi-Zoccai, Giuseppe G. L. ;
Lotrionte, Marzia ;
Agostoni, Pierfrancesco ;
Abbate, Antonio ;
Fusaro, Massimiliano ;
Burzotta, Francesco ;
Testa, Luca ;
Sheiban, Imad ;
Sangiorgi, Giuseppe .
EUROPEAN HEART JOURNAL, 2006, 27 (22) :2667-2674
[8]   Increased risk in patients with high platelet amregation receiving chronic clopidogrel therapy undergoing percutaneous coronary intervention - Is the current antiplatelet therapy adequate? [J].
Bliden, Kevin P. ;
DiChiara, Joseph ;
Tantry, Udaya S. ;
Bassi, Ashwani K. ;
Chaganti, Srivasavi K. ;
Gurbel, Paul A. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2007, 49 (06) :657-666
[9]   The Warfarin/Aspirin Study in Heart failure (WASH): A randomized trial comparing antithrombotic strategies for patients with heart failure [J].
Cleland, JGF ;
Findlay, I ;
Jafri, S ;
Sutton, G ;
Falk, R ;
Bulpitt, C ;
Prentice, C ;
Ford, I ;
Trainer, A ;
Poole-Wilson, PA .
AMERICAN HEART JOURNAL, 2004, 148 (01) :157-164
[10]   Antiplatelet therapy in percutaneous coronary intervention: is variability of response clinically relevant? [J].
Curzen, Nick ;
Sambu, Nalyaka .
HEART, 2011, 97 (17) :1433-1440