Free radical scavenger, edaravone, in stroke with internal carotid artery occlusion

被引:116
作者
Toyoda, K
Fujii, K
Kamouchi, M
Nakane, H
Arihiro, S
Okada, Y
Ibayashi, S
Iida, M
机构
[1] Natl Kyushu Med Ctr, Dept Cerebrovasc Dis, Fukuoka 8108563, Japan
[2] Natl Kyushu Med Ctr, Clin Res Inst, Fukuoka 8108563, Japan
[3] Fukuoka Red Cross, Stroke Ctr, Fukuoka, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Med & Clin Sci, Fukuoka, Japan
[5] Natl Ureshino Hosp, Dept Neurol & Strokol, Ureshino, Japan
[6] Hakujyuji Hosp, Stroke Ctr, Fukuoka, Japan
关键词
brain infarction; stroke management; stroke outcome; brain edema; hemorrhagic transformation; neuroprotective agent;
D O I
10.1016/j.jns.2004.03.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Edaravone has potent free radical quenching and antioxidant actions. The agent has been recently in commercial use for acute ischemic stroke patients. In this study, we investigated the therapeutic effect of edaravone on severe carotid-territorial stroke. Methods: Stroke patients with internal carotid artery occlusion and baseline NIH Stroke Scale Score greater than or equal to15 were treated for 14 days with drip intravenous infusion of edaravone (n=30) and were compared with a historical control cohort of similar patients (n=31). Glycerol was also administered to all patients in both groups. Results: Infarct volume (P<0.02) and midline shift (P<0.02) on CT performed on day 2 of the patients treated with edaravone were smaller than those without edaravone. For patients with edaravone, infarct volume (P<0.0001) and midline shift (P<0.0001) on days 5-7 were greater than those on day 2. Hemorrhagic transformation of infarcts on day 2 was less severe in patients with than without edaravone (P<0.03). Within 14 days after the onset of stroke, 6 patients with edaravone (20%) and 14 without edaravone (45%) died directly of stroke (P<0.03). Among all patients, only two treated with edaravone were independent without any assistance 8 weeks after the onset. Conclusions: Edaravone was associated with delayed evolution of infarcts and edema in patients with severe carotid-territorial stroke and decreased mortality during the acute stage. The agent, however, failed to prevent evolution of infarcts and edema on later days, and did not significantly improve functional outcome among the surviving patients. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 17
页数:7
相关论文
共 30 条
[1]   STRONG ATTENUATION OF ISCHEMIC AND POSTISCHEMIC BRAIN EDEMA IN RATS BY A NOVEL FREE-RADICAL SCAVENGER [J].
ABE, K ;
YUKI, S ;
KOGURE, K .
STROKE, 1988, 19 (04) :480-485
[2]   LEUKOTRIENES INCREASE BLOOD-BRAIN-BARRIER PERMEABILITY FOLLOWING INTRAPARENCHYMAL INJECTIONS IN RATS [J].
BLACK, KL ;
HOFF, JT .
ANNALS OF NEUROLOGY, 1985, 18 (03) :349-351
[3]   BRAIN EDEMA - INDUCTION IN CORTICAL SLICES BY POLY-UNSATURATED FATTY-ACIDS [J].
CHAN, PH ;
FISHMAN, RA .
SCIENCE, 1978, 201 (4353) :358-360
[4]   INDUCTION OF BRAIN EDEMA FOLLOWING INTRACEREBRAL INJECTION OF ARACHIDONIC-ACID [J].
CHAN, PH ;
FISHMAN, RA ;
CARONNA, J ;
SCHMIDLEY, JW ;
PRIOLEAU, G ;
LEE, J .
ANNALS OF NEUROLOGY, 1983, 13 (06) :625-632
[5]   Rapid breakdown of microvascular barriers and subsequent hemorrhagic transformation after delayed recombinant tissue plasminogen activator treatment in a rat embolic stroke model [J].
Dijkhuizen, RM ;
Asahi, M ;
Wu, O ;
Rosen, BR ;
Lo, EH .
STROKE, 2002, 33 (08) :2100-2104
[6]   'Malignant' middle cerebral artery territory infarction - Clinical course and prognostic signs [J].
Hacke, W ;
Schwab, S ;
Horn, M ;
Spranger, M ;
DeGeorgia, M ;
vonKummer, R .
ARCHIVES OF NEUROLOGY, 1996, 53 (04) :309-315
[7]  
HACKE W, 1995, JAMA-J AM MED ASSOC, V274, P1017, DOI 10.1001/jama.274.13.1017
[8]   REACTIVE OXYGEN SPECIES AND THE CENTRAL-NERVOUS-SYSTEM [J].
HALLIWELL, B .
JOURNAL OF NEUROCHEMISTRY, 1992, 59 (05) :1609-1623
[9]   Hemorrhagic transformation and microvascular integrity during focal cerebral ischemia/reperfusion [J].
Hamann, GF ;
Okada, Y ;
delZoppo, GJ .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (06) :1373-1378
[10]   MICROVASCULAR BASAL LAMINA ANTIGENS DISAPPEAR DURING CEREBRAL-ISCHEMIA AND REPERFUSION [J].
HAMANN, GF ;
OKADA, Y ;
FITRIDGE, R ;
DELZOPPO, GJ .
STROKE, 1995, 26 (11) :2120-2126