Key result
Intravenous naloxone produced prompt recovery in 7 of 20 patients with acute cerebral ischemia and 3 of 3 with hyperacute ischemia, but had no effect in established infarcts or hemorrhage.
Why the study?
Does intravenous naloxone differentiate reversible versus irreversible cerebral ischemia in patients with stroke?
Observational (n=48)
Does intravenous naloxone differentiate reversible versus irreversible cerebral ischemia in patients with stroke?
Intravenous naloxone may help differentiate reversible from irreversible cerebral ischemia in acute stroke patients.
Naloxone response may mark reversible ischemia in hyperacute stroke; case-report data leave open any diagnostic role.
Naloxone was given as an I.V. bolus of 0.8 mgs to four groups of patients with stroke: 1) 20 patients with C.T. proven cerebral infarcts of longer than 7 days duration; 2) 20 patients with acute cerebral ischemia of less than 24 hours; 3) 5 patients with C.T. proven intracerebral hemorrhage of less than 24 hours, and; 4) 3 patients with hyperacute cerebral ischemia which occurred during the performance of a cerebral angiogram. The patients with established cerebral infarctions of more than 7 days duration and the patients with intracerebral hematomas had no response to intravenous naloxone. Of 20 patients with acute cerebral ischemia of less than 24 hours duration, 7 had prompt, complete and long-lasting recovery. These patients had no subsequent evidence of cerebral infarct by C.T. scanner 48 hours after the onset of the cerebral ischemia and were asymptomatic when discharged. The 3 patients with hyperacute cerebral ischemia secondary to cerebral angiography had a dramatic response to the injection of naloxone. These findings suggest that intravenous naloxone may differentiate reversible versus irreversible cerebral ischemia.
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Estañol et al. (1985) conducted an observational in Stroke and cerebral ischemia (n=48). Naloxone was evaluated on Clinical response or recovery. Intravenous naloxone produced prompt recovery in 7 of 20 patients with acute cerebral ischemia and 3 of 3 with hyperacute ischemia, but had no effect in established infarcts or hemorrhage.
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