Cardiovascular Diseases Clinical Trial
To determine whether the administration of intravenous streptokinase (SK) early in the course of acute, transmural myocardial infarction would limit myocardial damage.
BACKGROUND:
Determination of the potential value of thrombolytic therapy in patients with acute
myocardial infarction was an issue of major importance in 1983. An estimated 1.4 million
heart attacks occurred each year, of which over 500,000 were fatal. Reduction of mortality
required an effective means to reduce infarct size. Studies indicated that reperfusion
represented a potent means of achieving salvage of ischemic myocardium. Pilot clinical
studies indicated that reperfusion could be achieved in a substantial percentage of patients
by lysis of coronary thrombosis with both intracoronary and intravenous streptokinase
administration. Intracoronary thrombolysis was receiving widespread clinical applications
but had many limitations. The intracoronary route took 90-120 minutes longer to administer
than the intravenous route. Because intracoronary therapy required the availability of a
catheterization laboratories and highly skilled invasive cardiologists, this treatment was
not available to large numbers of patients who were hospitalized in smaller community
hospitals.
DESIGN NARRATIVE:
Randomized design with two groups and fixed sample size. Control patients received routine
coronary care. The treatment group received intravenous streptokinase plus conventional
care. This was followed with intravenous heparin and warfarin. The primary endpoint was 14
day mortality. Secondary endpoints included angiographic patency of the involved coronary
artery at 10 to 14 days, left ventricular function, segmental wall motion analysis, and
myocardial infarction size at 30-45 days.
;
Allocation: Randomized, Primary Purpose: Treatment
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