We evaluated intravenous streptokinase in the treatment of cerebral in
farction. Following neurological assessment and cerebral computed tomo
graphy (CT), patients aged 40-80 years with symptoms of anterior circu
lation acute ischaemic stroke were given 1.5 M units streptokinase or
saline placebo in a double-blind randomized study. Twenty patients (10
streptokinase, 10 placebo), 11 males, 9 females, aged 57-79 years, we
re treated out of 512 consecutive admissions to the acute stroke unit
over a 2-year period. Initial CT was normal in 11 (6 placebo, 5 strept
okinase) and showed early signs of cerebral infarction in nine (4 plac
ebo, 5 streptokinase). Median times from symptom onset to treatment we
re 5.2 h (placebo) and 5.8 h (streptokinase), Streptokinase treatment
was associated with symptomatic hypotension in one patient. Repeat CT
at 72 h demonstrated intracerebral haematoma in two patients and haemo
rrhagic infarction in one patient in the streptokinase group; the two
cases of haematoma formation were associated with neurological deterio
ration and death. One patient in the placebo group had evidence of hae
morrhagic infarction at 72 h. There were three deaths in each treatmen
t group, all within the first 14 days. Patients with acute stroke can
be evaluated with CT and treated with streptokinase within 6 h, but th
e opportunity for treatment is currently limited to few patients. Stre
ptokinase treatment is not without risk, but potential clinical benefi
t justifies ongoing multicentre randomized trials.