Stroke, Vol 21, 721-725, Copyright © 1990 by American Heart Association
CP Olinger, HP Adams Jr, TG Brott, J Biller, WG Barsan, GJ Toffol, RW Eberle and JR Marler
To evaluate the safety and possible efficacy of high-dose naloxone for the
treatment of acute cerebral ischemia, 38 patients received a loading dose
of 160 mg/m2 over 15 minutes followed by a 24-hour infusion at the rate of
80 mg/m2/hr. Nausea and/or vomiting were common side effects. Naloxone was
discontinued in seven patients (because of hypotension in one, bradycardia
and hypotension in two, myoclonus in one, focal seizures in two, and
hypertension in one); all seven patients responded to treatment and no
permanent sequelae to naloxone were noted. Twelve of the 38 patients showed
early neurologic improvement (by completion of the naloxone loading dose).
However, there was no correlation between such a loading dose response and
clinical outcome at 3 months. Our experience suggests that naloxone is safe
at the dose used, but data for efficacy are inconclusive.
ARTICLES
High-dose intravenous naloxone for the treatment of acute ischemic stroke
Department of Neurology, University of Cincinnati, Ohio.
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