Clopidogrel: the future choice for preventing platelet activation during coronary stenting?

Published

Journal Article (Review)

Ticlopidine has become an established therapy in patients with stroke, and during stenting in patients with coronary artery disease. Clopidogrel, another thienopyridine, is a safe and promising alternative, that irreversibly inhibits ADP-induced platelet aggregation, and reduces formation of both arterial and venous thrombi. In a recent, large, well-controlled trial (CAPRIE), clopidogrel has been shown to be superior to aspirin in terms of prevention of ischaemic stroke, myocardial infarction and death in patients with atherosclerotic vascular disease. Clopidogrel provides a safe opportunity to enhance reperfusion when administered during stent placement, by protecting platelets from excessive activation. However, the ability of clopidogrel to be superior to ticlopidine in terms of its antiplatelet properties in the clinical setting of coronary stenting, is unknown. The effects of clopidogrel versus ticlopidine on platelet and endothelial function are yet to be determined and may strongly affect the outcome, benefits, and complications following coronary stent placement. Further clinical trials, well-designed, and carefully conducted, should elucidate possible benefits of clopidogrel during coronary interventions, especially in conjunction with new and aggressive reperfusion techniques. The benefits of clopidogrel in an expanding array of clinical conditions, including myocardial infarction, may be directly related to platelet inhibition. Moreover, marginal clinical benefits, and recently reported severe bleeding events in some patients after oral platelet glycoprotein IIb/IIIa therapy, may advance clopidogrel as a safe, and efficient alternative during coronary interventions. This review summarises the latest, and often confusing data on the effects of thienopyridines on certain haemostatic characteristics in interventional cardiology. 1999 Academic Press.

Full Text

Duke Authors

Cited Authors

  • Gurbel, PA; O'Connor, CM; Cummings, CC; Serebruany, VL

Published Date

  • August 1999

Published In

Volume / Issue

  • 40 / 2

Start / End Page

  • 107 - 111

PubMed ID

  • 10433868

Pubmed Central ID

  • 10433868

Electronic International Standard Serial Number (EISSN)

  • 1096-1186

International Standard Serial Number (ISSN)

  • 1043-6618

Digital Object Identifier (DOI)

  • 10.1006/phrs.1999.0478

Language

  • eng