Editorial
Copyright ©2010 Baishideng Publishing Group Co.
World J Cardiol. Jun 26, 2010; 2(6): 131-134
Published online Jun 26, 2010. doi: 10.4330/wjc.v2.i6.131
Table 1 Alternatives to clopidogrel for patients with acute coronary syndromes
DrugMain featuresProsCons
CilostazolPhosphodiesterase inhibitor with antiplatelet and antirestenotic effects, also indicated for the medical treatment of claudicationDifferent mechanism of action translates into increased antithrombotic efficacy when used in combination with aspirin and a thienopyridineTolerability limited by gastro-intestinal side effects in up to 20% of patients
Oral anticoagulantsSeveral agents directly or indirectly inhibiting the coagulation process, including warfarin and dabigatranDifferent mechanism of action translates into increased antithrombotic efficacy when used in combination with aspirinSpecificity for the coagulation process translates into lower efficacy on thrombotic processes largely dependent on platelets (such as stent thrombosis). Narrow therapeutic window and need for frequent monitoring (warfarin) translates in higher incidence of bleeding complications
PrasugrelThird-generation thienopyridine irreversibly inhibiting the P2Y12 receptor, with quicker, more consistent and more potent action than clopidogrelPotency and consistency of effect enable homogeneous and nearly complete platelet aggregation inhibition in most patients, with ensuing benefits on myocardial infarction and stent thrombosisGreater potency may translate into bleeding risk overcoming ischemic benefits in those at moderate or high bleeding risk, such as the elderly and those with previous stroke or transient ischemic attack
TicagrelorNon-thienopyridine agent reversibly inhibiting the P2Y12 receptor, with quicker, more consistent, and more potent action, but shorter half-life than clopidogrelDirect action translates into quicker onset of action and lack of interaction with drugs metabolized by cytochrome P450, such as proton pump inhibitorsShorter half-life may translate into greater risk of thrombotic recurrences in case of non-compliance
TiclopidineFirst-generation thienopyridine irreversibly inhibiting the P2Y12 receptor, with longer half-life than clopidogrelLimited cross-unresponsiveness translates into potential role in those lacking complete response to clopidogrel. Off-patent status translates into low costLower tolerability with frequent gastro-intestinal adverse effects. Rarely but significantly associated with life-threatening agranulocytosis and thrombotic thrombocytopenic purpura