Stroke, Vol 24, 1452-1457, Copyright © 1993 by American Heart Association
A Bellavance
BACKGROUND AND PURPOSE: This subgroup analysis from the Ticlopidine Aspirin
Stroke Study (TASS) compared ticlopidine, a new antiplatelet agent, with
aspirin for the prevention of recurrent transient ischemic attacks in
patients who had a recent reversible cerebrovascular event. METHODS: This
was a multicenter, double-blind, randomized trial in patients with a recent
cerebral ischemic history. Patients with a reversible cerebral ischemic
event within 3 months of enrollment were eligible for the study. All
patients received either aspirin 650 mg twice daily or ticlopidine 250 mg
twice daily for up to 5.8 years. The primary end point in this analysis was
the first occurrence of a reversible ischemic event either alone or
combined with nonfatal stroke or death and fatal or nonfatal stroke.
RESULTS: Overall, ticlopidine was better than aspirin for reducing the risk
of reversible ischemic events either alone or as a composite with death
and/or stroke or with fetal and/or nonfatal stroke (P = .007 to P <
.001). The risk reductions with ticlopidine were maintained for the
duration of the 5- year follow-up. The most frequent or clinically
important adverse effects associated with ticlopidine were diarrhea, rash,
and neutropenia. Neutropenia was severe in 13 patients but resolved
promptly with discontinuation of therapy. CONCLUSIONS: The results in this
subgroup of patients with reversible ischemic disease, as well as the
overall analysis of TASS, suggest that ticlopidine is a more effective
agent than aspirin for the prevention of recurrent transient ischemic
attacks.
ARTICLES
Efficacy of ticlopidine and aspirin for prevention of reversible cerebrovascular ischemic events. The Ticlopidine Aspirin Stroke Study
Department of Medicine, University of Sherbrooke at Charles LeMoyne Hospital, Quebec, Canada.
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