Copyright © 1994 by the European Society of Cardiology.
© 1994 The European Society of Cardiology
Ridogrel does not increase the speed and rate of coronary recanalization in patients with myocardial infarction treated with alteplase and heparin


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*From the Instituto do Coraçao (INCOR), University of Sao Paulo Sao Paulo, Brasil
Janssen Research Division Beerse, Belgium
Department of Cardiology, University Hospital Gasthuisberg Leuven, Belgium
Center for Molecular and Vascular Biology, University of Leuven Belgium
Received 28 September 1993; revised 27 December 1993; .
Correspondence. Prof. Marc Verstraete, MD, PhD, Center for Molecular and Vascular Biology, University of Leuven, Campus Gasthuisberg, O & N, Herestraat 49, B-3000 Leuven, Belgium.
Abstract
Ridogrel, a compound with the dual property of inhibiting the synthesis of thromboxane and blocking the receptors of thromboxanelprostaglandinlendoperoxides, has been shown to accelerate the speed of recanalization and to delay or prevent reocclusion during systemic thrombolysis with tissue plasminogen activator in experimental animals. Ninety patients who had not taken any antiplatelet drugs within the last 10 days were randomized to either intravenous ASA 250 mg immediately before the thrombolytic treatment and 100 mg once a day orally thereafter or ridogrel 300 mg i. v. before thrombolytic treatment and 300 mg b.i.d. orally thereafter. All patients were given intravenous heparin concomitantly with alteplase. The patency of the infarct-related artery was determined by coronary angiography before the administration of the thrombolytic agent and by repeated coronary angiography every 15 min until the end of the administration of alteplase. A final angiogram was obtained 48 to 72 h later. At 90 min, the recanalization and patency rates were the same in the two treatment groups with no intergroup difference in the speed of recanalization.
Key Words: Alteplase coronary thrombolysis ridogrel myocardial infarction
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