Thrombolytic therapy has become standard care in treating acute myocar
dial infarction. Fibrinolytic drugs such as streptokinase, APSAC and u
rokinase are non fibrin specific, and induce systemic activation of th
e fibrinolytic process, while t-PA and prourokinase are fibrin specifi
c since they are able to activate mainly fibrin bound plasminogen. Bot
h groups of thrombolytics exert different and opposing effects on the
hemostatic balance: indeed, they have antithrombotic as well as prothr
ombotic properties, and this may be important for explaining therapeut
ic failures or reocclusions. New strategies have been considered or ar
e under investigation for further improving the already excellent effi
cacy of thrombolytic treatment in myocardial infarction: combined admi
nistration of fibrinolytic agents, thrombus-targeted thrombolytic drug
s, association with other drugs both effective and ineffective on the
hemostatic process. At present, however, the first priority still Seem
s to be a continuing effort to increase the percentage of patients tre
ated with thrombolytics, since the benefits of this therapy have alrea
dy been clearly demonstrated.