The Australian Streptokinase Trial was a randomized, double-blind, pla
cebo-controlled trial, in which streptokinase (SK, 1.5 million IU TV)
was given within 4 hours of stroke onset. In a subset of 37 patients,
Tc-99m-labeled D,L-hexamethylpropylene amine oxime single-photon emiss
ion computed tomography (SPECT) and/or transcranial Doppler (TCD) stud
ies were performed before and after therapy to test the hypothesis tha
t SK may improve the hemodynamic measures of reperfusion/recanalizatio
n rates (TCD parameter) within 24 hours. Eighteen patients received SK
and 19 placebo. Baseline characteristics were similar in both groups,
and there were no differences in clinical outcomes assessed at 3 mont
hs after stroke. Although there was no increase in the group mean perf
usion defect or volume on SPECT after thrombolytic therapy, a larger n
umber of patients demonstrating the combined end point of reperfusion
or recanalization was seen in the SK group (13/14, 93%) than in the pl
acebo group (7/14, 50%; p = 0.01). Although SK given within 4 hours of
acute ischemic stroke appears to improve arterial patency/tissue repe
rfusion, this effect is neither early nor extensive enough to influenc
e overall clinical outcome.