(Circulation. 2001;103:2862.)
© 2001 American Heart Association, Inc.
Cardiovascular Drugs |
From the University of Alberta, Edmonton, Alberta, Canada (P.W.A.), and Katholieke Universiteit Leuven, Leuven, Belgium (D.C.).
Correspondence to Paul W. Armstrong, MD, 2-51 Medical Sciences Bldg, University of Alberta, Edmonton, Alberta T6G 2H7, Canada. E-mail paul.armstrong@ualberta.ca
Key Words: fibrinolysis myocardial infarction drugs
| Introduction |
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Since this subject was last reviewed in 1998 in the New Frontiers Section of Circulation, there have been 2 additional fibrinolytic agents released for clinical application and 1 other that has undergone major and extensive phase 2 and 3 investigation.1 Although streptokinase (SK), recombinant tissue plasminogen activator (rt-PA), and more recently reteplase (r-PA) are in general clinical use, there remains some dissatisfaction with their overall efficacy. This relates in part to the failure to achieve optimal tissue reperfusion in approximately one half of patients so treated, as well as persistent risks associated with systemic hemorrhagic effects, some of which complicate ancillary vascular interventional procedures in complicated patients. The risk of intracranial hemorrhage, affecting 5 to 10 of 1000 patients treated, remains a dreaded complication.2
In this review, we examine (1) the evolution of the development of fibrinolytics; (2) the pharmacology, pharmacokinetics, and pharmacodynamics of available agents; (3) the need for ancillary therapy; (4) the clinical indications, benefits and risks; (5) the therapeutic alternatives to fibrinolysis; and (6) the future developments that are likely to affect the application of this therapy.
| Evolution of Fibrinolysis |
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