Emergency administration of abciximab for treatment of patients with acute ischemic stroke -: Results of a randomized phase 2 trial

被引:110
作者
Adams, HP [1 ]
Hacke, W [1 ]
Oemar, B [1 ]
Dávalos, A [1 ]
Cook, RA [1 ]
Trouillas, P [1 ]
Fazekas, F [1 ]
Bogousslavsky, J [1 ]
Hilburn, J [1 ]
Torner, J [1 ]
Leclerc, J [1 ]
Shuaib, A [1 ]
Reid, P [1 ]
机构
[1] Univ Iowa, Dept Neurol, Iowa City, IA 52242 USA
关键词
antiplatelet agents; emergency medical treatment; stroke;
D O I
10.1161/01.STR.0000157668.39374.56
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 mu g/kg per minute (maximum 10 mu g/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.
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页码:880 / 890
页数:11
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