Stroke, Vol 19, 716-722, Copyright © 1988 by American Heart Association
CY Hsu, JW Norris, EL Hogan, P Bladin, HB Dinsdale, FM Yatsu, MP Earnest, P Scheinberg, LR Caplan and HR Karp
The efficacy and safety of pentoxifylline were assessed in 297 adult
patients with ischemic stroke in a multicenter, double-blind, randomized
and placebo-controlled trial. Treatment was started within 12 hours after
the stroke onset. Study medication was administered intravenously
continuously (16 mg/kg/day, maximum 1,200 mg/day) for 3 days and per os
(400 mg t.i.d.) for the remainder of 28 days. Demographic data were
comparable, and functional impairment and mortality (pentoxifylline 12%,
placebo 10%) were not different between the two groups. Neurologic deficit
scores improved from baseline admission scores during the 4-week study in
both groups but did not differ between groups at admission or throughout
the study except during the first few days when the consciousness level
(Days 1 and 2), motor function (Days 1 and 2), cranial nerve function (Days
1-4), and total neurologic deficit scores (Days 1 and 2) were better in the
pentoxifylline group than in the placebo group, especially in a subset of
patients with severe deficits at admission. Laboratory values and side
effects were also comparable between groups. Our study indicates that
pentoxifylline can be given safely in patients with acute ischemic stroke.
Although pharmacologic effects were present during the first few days, the
clinical benefits were small and not sustained.
ARTICLES
Pentoxifylline in acute nonhemorrhagic stroke. A randomized, placebo- controlled double-blind trial
Department of Neurology, Medical University of South Carolina, Charleston 29425.
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