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on February 24, 2005

Stroke. 2005
Published online before print February 24, 2005, doi: 10.1161/01.STR.0000157668.39374.56
A more recent version of this article appeared on April 1, 2005
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Submitted on September 7, 2004
Revised on December 1, 2004
Accepted on December 21, 2004

Emergency Administration of Abciximab for Treatment of Patients With Acute Ischemic Stroke. Results of a Randomized Phase 2 Trial

Abciximab Emergent Stroke Treatment Trial (AbESTT) Investigators

Background and Purpose--Because of its success in treatment of acute cardiac ischemia, there is interest in the use of abciximab for treating patients with acute ischemic stroke. A previous dose-escalation study determined that abciximab could be given safely in a regimen of 0.25 mg/kg intravenous bolus followed by a 12-hour infusion at 0.125 µg/kg per minute (maximum 10 µg/min). This study was performed to obtain more information about the safety and potential efficacy of abciximab in patients with stroke.

Methods--An international randomized, double-blind, placebo-controlled phase 2 trial enrolled 400 patients within 6 hours of onset of ischemic stroke. The primary safety outcome was the rate of symptomatic hemorrhage that occurred during the first 5 days after stroke. The primary efficacy measure was the distribution of outcomes at 3 months after stroke using the modified Rankin Scale (mRS) based on an ordinal regression model of outcomes, adjusting for baseline severity of stroke, age, and interval from stroke.

Results--Symptomatic intracranial hemorrhage within 5 days was diagnosed in 7 of 195 (3.6%) patients treated with abciximab and 2 of 199 (1%) patients given placebo (odds ratio [OR], 3.7; P=0.09; 95% confidence interval [CI], 0.7 to 25.9). Asymptomatic hemorrhagic transformation was detected by brain imaging in 24 patients administered abciximab and 33 patients receiving placebo (OR, 0.74; P=0.25; 95% CI, 0.4 to 1.3). Treatment with abciximab showed a nonsignificant shift in favorable outcomes as measured by mRS scores at 3 months (OR, 1.20; P=0.33; 95% CI, 0.84 to 1.70).

Conclusions--Intravenously administered abciximab can be given to patients with a reasonable degree of safety. The trial also suggests that abciximab could improve outcomes at 3 months after stroke. A larger randomized, double-blind, placebo-controlled trial is necessary to test the efficacy of abciximab.


Key words: antiplatelet agents • emergency medical treatment • stroke




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