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Efficacy and safety of edaravone in treatment of amyotrophic lateral sclerosisa systematic review and meta-analysis

机译:埃及龙酮治疗肌营养外阴肺活灭系统综述及荟萃分析的疗效和安全性

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BackgroundBased on the results of randomized, double-blind, placebo-controlled trials, the benefit and safety of edaravone in the treatment of amyotrophic lateral sclerosis remain controversial. We performed a meta-analysis to evaluate the efficacy and safety of edaravone in the treatment of this disease.MethodsWe searched PubMed, the Cochrane Library, and Embase from the inception of electronic data to April 2018. We included randomized, double-blind, placebo-controlled trials reporting amyotrophic lateral sclerosis patients receiving 60-mg intravenous edaravone or intravenous saline placebo for 24weeks. The primary efficacy evaluation was changed in Amyotrophic Lateral Sclerosis Functional Rating Scale score from baseline to after the trial. Measure of safety was the frequency of investigated adverse events and serious adverse events. Data synthesis and analysis and evaluation of risk of bias were performed using RevMan 5.3 software. Heterogeneity among studies was evaluated with the I-2 statistic.ResultsA total of 367 patients were analyzed across three randomized controlled trials (183 patients receiving intravenous edaravone; 184 receiving placebo). A difference in ALSFRS-R score between groups at 24weeks was found (mean difference [MD]=1.63, 95% confidence interval [CI] 0.26-3.00, P=.02). No differences in the frequency of adverse events (odds ratio [OR]=1.22, 95% CI 0.68-2.19, P=.50) or serious adverse events (OR=0.71, 95% CI 0.43-1.19, P=.20) were found.ConclusionIntravenous edaravone is efficacious in amyotrophic lateral sclerosis patients, with no severe adverse effects. Additional reliable randomized controlled trials with larger sample sizes will further assess the efficacy and safety of edaravone in amyotrophic lateral sclerosis.Clinical trial registrationThe systematic review and meta-analysis was registered in the international prospective register of systematic reviews. (PROSPERO registration number: CRD42018096191; http://www.crd.york.ac.uk/PROSPERO.)
机译:背景基于随机,双盲,安慰剂对照试验,赤纬治疗肌营养侧面硬化症治疗的益处和安全性仍存在争议。我们进行了一个荟萃分析,以评估埃达拉夫松治疗该疾病的疗效和安全性。近奇地区搜查了PubMed,Cochrane图书馆,并从电子数据的开始到2018年4月。我们包括随机,双盲,安慰剂 - 核对试验报告肌营养的侧链患者接受60毫克静脉内赤纬饲养或静脉注射盐水安慰剂24周。初级疗效评估在肌萎缩侧面硬化功能评级规模评分从基线进行改变,试验后。衡量安全性是调查不良事件的频率和严重不良事件。使用Revman 5.3软件进行数据综合和分析和偏置风险的评估。通过I-2统计评估研究中的异质性。患有367名患者的367例,在三次随机对照试验中分析了367名患者(183名接受静脉浸润的患者; 184次接受安慰剂)。发现了24周的组之间的ALSFRS-R分数的差异(平均差异[MD] = 1.63,95%置信区间[CI] 0.26-3.00,P = .02)。不良事件的频率没有差异(差距[或] = 1.22,95%CI 0.68-2.19,p = .50)或严重不良事件(或= 0.71,95%CI 0.43-1.19,P = .20)被发现.ConclusionIntravenous eDaravone在肌萎缩侧面硬化症患者中有效,没有严重的不良反应。具有较大样本尺寸的其他可靠随机对照试验将进一步评估埃及龙酮在肌营养的侧面硬化症中的疗效和安全性。临床试验登记系统审查和Meta分析在国际上审查的国际未来登记册中登记。 (Prospero注册号:CRD42018096191; http://www.crd.york.ac.uk/pospero。)

著录项

  • 来源
    《Neurological sciences》 |2019年第2期|共7页
  • 作者单位

    Southern Med Univ Affiliated Xiaolan Hosp Dept Neurol Zhongshan Peoples R China;

    Southern Med Univ Affiliated Xiaolan Hosp Dept Neurol Zhongshan Peoples R China;

    Southern Med Univ Affiliated Xiaolan Hosp Dept Neurol Zhongshan Peoples R China;

    Southern Med Univ Affiliated Xiaolan Hosp Dept Neurol Zhongshan Peoples R China;

    Southern Med Univ Affiliated Xiaolan Hosp Dept Neurol Zhongshan Peoples R China;

    Southern Med Univ Affiliated Xiaolan Hosp Dept Neurol Zhongshan Peoples R China;

    Southern Med Univ Affiliated Xiaolan Hosp Dept Neurol Zhongshan Peoples R China;

    Southern Med Univ Affiliated Xiaolan Hosp Dept Neurol Zhongshan Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 神经病学与精神病学;
  • 关键词

    Amyotrophic lateral sclerosis; Edaravone; ALSFRS-R score;

    机译:肌萎缩的外侧硬化;埃达拉夫酮;alsfrs-r得分;

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