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机构地区:[1]嘉应学院医学院附属医院内科,梅州514031 [2]湖南省永州市人民医院神经内科,423000
出 处:《中国医疗前沿》2010年第8期48-49,共2页China Healthcare Innovation
摘 要:目的探讨神经节苷脂联合依达拉奉治疗大面积脑梗死的临床疗效。方法将发病48h内的大面积脑梗死的病人74例,随机分入治疗组和对照组。对照组应用神经节苷脂注射液60mg静脉滴注,1次/d,共21d,同时给予阿司匹林、低分子肝素作为基础治疗;治疗组应用神经节苷脂注射液60mg,1次/d,同时给予依达拉奉注射液30mg静脉滴注,2次/d,共21d。发病72h和治疗后定期对患者行欧洲卒中评分(ESS)、日常生活活动能力(ADL)评分,以治疗21dESS的评分和第90d的ADL评分作为主要疗效判断标准。结果21d后联合治疗组和对照组的ESS评分分别为(67.32±15.36)、(50.21±13.04),两组相比差异有显著性(p<0.01);90d后治疗组、对照组ADL(改良Barthel指数)评分分别为(75.38±20.56)、(54.63±28.59),两组相比有差异有显著性(p<0.01)。结论神经节苷脂联合依达拉奉治疗大面积脑梗死疗效明显。Objective Purpose To explore the therapeutic effects of of ganglioside GM-1 and edaravone for severe cerebral infarction. Methods 74 patients with severe cerebral infarcdon within 48 hours after the onset of stroke symptom were randomly assigned to receive ganglioside GM-1 and edaravone (n=38) or ganglioside GM-1 (control group,n=36). Ganglioside GM-1 and edaravone were infused at a dose of 60mg per day or 30mg twice a day,respectively,for 21 days. Meanwhile aspirin and low-molecular-weight heparin were used as basic treatment.72h after onset and 21 days and 3 months after treatment,the neurological deficits were evaluated with the use of European Stroke Scale (ESS) and activities of daily living (ADL). Results There were significant differences in ESS between GM-1 group and control group at 21 day (67.32±15.36 Vs.50.21±13.04,p〈 0.01). There were also significant differences in ADL at 90 day between the groups (75.38±20.56 Vs 54.63±28.59,p〈 0.01). Conclusion Ganglioside GM-1 and edaravone has a goodtherapeutic effect for severe cerebral infarction.
分 类 号:R743.33[医药卫生—神经病学与精神病学]
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