Effect of a Novel Free Radical Scavenger, Edaravone (MCI-186), on Acute Brain Infarction

依达拉奉 医学 自由基清除剂 改良兰金量表 神经保护 安慰剂 蛛网膜下腔出血 麻醉 冲程(发动机) 内科学 缺血 缺血性中风 病理 氧化应激 替代医学 工程类 机械工程
作者
Wolfgang Müllges,D Franke,Wilko Reents,Jörg Babin‐Ebell,Klaus V. Toyka,Nerissa Ko,Steven Johnston,William L. Young,Vikrant Singh,Arthur L. Klatsky,Filipa Falcão,Norbert G. Campeau,Eelco F. M. Wijdicks,John L.D. Atkinson,Jimmy R. Fulgham,Raymond T.F. Cheung,Pui Wai Cheng,Wai Man Lui,Gilberto K.T. Leung,Ting‐Yim Lee,Stefan T Engelter,James M. Provenzale,Jeffrey R. Petrella,David M. DeLong,Mark J. Alberts,Stefan Evers,Darius G. Nabavi,Alexandra Rahmann,Christoph Heese,D. Reichelt,I. W. Husstedt,Antonio Araúz,Leora Velásquez,Carlos Cantú,Juan Náder,Marisol López López,Luis Murillo,Yolanda Aburto-Murrieta,Patrizia Nencini,Cristina Sarti,Rinaldo Innocenti,Giovanni Pracucci,Domenico Inzitari,Kyoung Heo,Sun Ah Park,Jong Yun Lee,Ki Young Lee,Seung Koo Lee,Patrı́cia Canhão,José M. Ferro,Dénes Páll,Georgios Settakis,Éva Katona,László Csiba,G. Kakuk,M. Limburg,Dániel Bereczki,Béla Fülesdi,Maurizio Paciaroni,Valeria Caso,Gabriela Cardaioli,Francesco Corea,Paolo Milia,Michele Venti,Mohammed Hamam,G.P. Pelliccioli,Lucilla Parnetti,Virgilio Gallai,Thanh G. Phan,John Huston
出处
期刊:Cerebrovascular Diseases [S. Karger AG]
卷期号:15 (3): 222-229 被引量:622
标识
DOI:10.1159/000069318
摘要

Edaravone, a novel free radical scavenger, demonstrates neuroprotective effects by inhibiting vascular endothelial cell injury and ameliorating neuronal damage in ischemic brain models. The present study was undertaken to verify its therapeutic efficacy following acute ischemic stroke. We performed a multicenter, randomized, placebo-controlled, double-blind study on acute ischemic stroke patients commencing within 72 h of onset. Edaravone was infused at a dose of 30 mg, twice a day, for 14 days. At discharge within 3 months or at 3 months after onset, the functional outcome was evaluated using the modified Rankin Scale. Two hundred and fifty-two patients were initially enrolled. Of these, 125 were allocated to the edaravone group and 125 to the placebo group for analysis. Two patients were excluded because of subarachnoid hemorrhage and disseminated intravascular coagulation. A significant improvement in functional outcome was observed in the edaravone group as evaluated by the modified Rankin Scale (p = 0.0382). Edaravone represents a neuroprotective agent which is potentially useful for treating acute ischemic stroke, since it can exert significant effects on functional outcome as compared with placebo.
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