Copyright © 2004 by the European Society of Cardiology.
Editorial
Are we making efficient use of clopidogrel?
Deutsches Herzzentrum and 1. Med. Klinik rechts der Isar, Technische Universität München, Lazarettstr. 36, Munich, Germany
Institut für Pharmakologie, Klinikum der Universitat zu Köln, Cologne, Germany
* Correspondence to: Tel.: +49-8912184577; fax: +49-8912184593
E-mail address: kastrati@dhm.mhn.de
| The first 10% of the full text of this article appears below. |
This editorial refers to "Limited early antiplatelet effect of 300 mg clopidogrel in patients with aspirin therapy undergoing percutaneous coronary interventions"1 by Lepäntalo et al. on page 476
Blood platelets play a major role in the occurrence of thrombotic complications after percutaneous coronary interventions (PCI). Introduction of the thienopyridine drug ticlopidine as an adjunctive antiplatelet therapy has considerably improved the outcome of patients who undergo PCI.1 Thienopyridines act via blockade of one (P2Y12) of the three adenosine 5
-diphosphate (ADP) receptors, reducing ADP-induced platelet activation and aggregation.2 Concerns about the side effects of ticlopidine, especially severe neutropenia and thrombotic thrombocytopenic purpura, were a major reason for the rapid replacement of this drug with clopidogrel. Another important limitation of ticlopidine is its delayed
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Related articles in EHJ:
- Limited early antiplatelet effect of 300 mg clopidogrel in patients with aspirin therapy undergoing percutaneous coronary interventions
- Aino Lepäntalo, Kari S Virtanen, Juhani Heikkilä, Ulla Wartiovaara, and Riitta Lassila
EHJ 2004 25: 476-483.[Abstract] [FREE Full Text]
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