Stroke, Vol 20, 317-323, Copyright © 1989 by American Heart Association
Patients with acute ischemic stroke were randomized less than 24 hours
after onset to standard (S) therapy (n = 43) or to hypervolemic
hemodilution (HH) with pentastarch (n = 45). The therapeutic goal of
hypervolemic hemodilution was to rapidly reduce hematocrit to 33%, to raise
cardiac output, and to continue hypervolemic hemodilution for 3 days. A
graded neurologic examination was scored by a blinded observer at
randomization (baseline), at the end of treatment or after 72 hours, and at
a 3-month follow-up; each patient was also rated using Barthel's disability
scale at the 3-month follow-up. Group demographics and results of the
graded neurologic examination were similar at baseline, except that the HH
group contained twice the number of patients with severe strokes and fewer
patients randomized within 12 hours compared with the S group. The HH group
improved an average of 7 points in neurologic score from baseline to the
end of treatment (the S group deteriorated 1 point) and 24 points by the
3-month follow-up (the S group improved 16 points; p = 0.11). The HH group
reached an average Barthel disability scale index of 85 while the S group
averaged 70 (p = 0.8). Deaths associated with cerebral edema occurred in
five patients with severe stroke (four in the HH group vs. one in the S
group, p = 0.36). The following subgroups of HH patients showed better
overall improvement in neurologic scores: patients entered within 12 hours
after stroke onset, patients with a 15% decrease in hematocrit, and
patients with a 10% increase in cardiac output.(ABSTRACT TRUNCATED AT 250
WORDS)
ARTICLES
Hypervolemic hemodilution treatment of acute stroke. Results of a randomized multicenter trial using pentastarch. The Hemodilution in Stroke Study Group
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