Circulation, Vol 89, 1567-1572, Copyright © 1994 by American Heart Association
RM Lidon, P Theroux, J Lesperance, B Adelman, R Bonan, D Duval and J Levesque
BACKGROUND: The success of streptokinase in acute myocardial infarction is
hampered by the high failure rate to achieve early reperfusion. This study
evaluates the possible benefit of Hirulog (Biogen, Cambridge, Mass), a
direct thrombin inhibitor, as adjunct therapy to streptokinase to enhance
early patency and prevent rethrombosis. Heparin has been shown to be of
very limited benefits in this setting. METHODS AND RESULTS: Forty-five
patients were randomized to Hirulog or heparin (2:1 ratio). Coronary
angiography documented a TIMI 2 or 3 flow after 90 minutes in 77% of the
patients treated with Hirulog and streptokinase and in 47% of patients
treated with heparin and streptokinase (P < .05) and after 120 minutes
in 87% and 47% of patients, respectively (P < .01). TIMI 3 flow was
established in 77% of patients with Hirulog compared with 40% with heparin
(P < .02). The clinical outcome and the bleeding rate was also favorable
to Hirulog; no reocclusion was observed at late angiography performed 4.7
days later. CONCLUSIONS: Hirulog in this pilot study significantly improved
the early patency rate of the infarct-related artery with a favorable
clinical profile. This new direct thrombin inhibitor exhibits promise as
adjunctive therapy to thrombolysis.
ARTICLES
A pilot, early angiographic patency study using a direct thrombin inhibitor as adjunctive therapy to streptokinase in acute myocardial infarction
Department of Medicine, Montreal Heart Institute, Quebec, Canada.
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