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以乌梅丸为主的干预措施治疗腹泻型肠易激综合征的Meta分析
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  • 英文篇名:Meta-analysis of Intervention Measures based on Plum Pills for the Treatment of Diarrhea Type Irritable Bowel Syndrome
  • 作者:丁晓洁 ; 杨毅 ; 于东林 ; 徐文娟 ; 董正平
  • 英文作者:Ding Xiaojie;Yang Yi;Yu Donglin;Xu Wenjuan;Dong Zhengping;School of Integrated Medicine, Binzhou Medical University;
  • 关键词:乌梅丸 ; 腹泻型肠易激综合征 ; 随机对照试验 ; Meta分析
  • 英文关键词:Plum Pill(Wumei Pill);;diarrhea type irritable bowel syndrome(IBS-D);;randomized controlled trial(RCT);;meta-analysis
  • 中文刊名:SJKX
  • 英文刊名:Modernization of Traditional Chinese Medicine and Materia Medica-World Science and Technology
  • 机构:滨州医学院中西医结合学院;
  • 出版日期:2019-04-20
  • 出版单位:世界科学技术-中医药现代化
  • 年:2019
  • 期:v.21
  • 基金:山东省自然科学基金委联合专项(ZR2015CL046):基于方证对应理论的肾阴虚证的细化分类研究,负责人:杨毅;; 山东省中医药管理局山东省中医药科技发展计划项目(2017-230):乌梅丸治疗寒热错杂型腹泻型肠易激综合征的疗效及干预肠道菌群和神经递质机制的临床研究,负责人:董正平
  • 语种:中文;
  • 页:SJKX201904006
  • 页数:7
  • CN:04
  • ISSN:11-5699/R
  • 分类号:52-58
摘要
目的:探讨以乌梅丸为主的干预措施治疗腹泻型肠易激综合征(IBS-D)的有效性和安全性,为临床推广提供科学依据。方法:通过文献筛选纳入以乌梅丸为主的干预措施治疗IBS-D的随机对照临床研究,用Cochrane评价方法对文献进行偏倚风险评估;并收集文献的发表时间、研究者、样本量、研究对象性别、干预措施、疗程、结局指标,利用Revman 5.3软件对数据进行Meta分析。结果:共纳入10篇符合要求的文献,Meta分析结果显示:与不含乌梅丸的干预措施相比,含乌梅丸的干预措施治疗IBS-D的综合疗效合并效应量RR=1.19,95%CI[1.11,1.26],差别具有统计学意义(P <0.05)。与单用西药的干预措施相比,含乌梅丸的干预措施的综合疗效的合并效应量RR=1.18,95%CI[1.10,1.26]差别具有统计学意义(P <0.05)。异质性检验没有统计学差异。所有研究的乌梅丸试验组未报告有不良反应。结论:以乌梅丸为主的干预措施治疗IBS-D有更好的临床疗效,安全性较好,适合临床推广使用。
        Objective: To discuss the effectiveness and safety of intervention measures based on Plum Pills in the treatment of diarrhea type irritable bowel syndrome(IBS-D). Method: Randomized controlled trials(RCTs) about Plum Pill and its modified prescriptions in treating IBS-D were included. Their bias risk was assessed by the Cochrane scale.The published time, researchers, sample size, subjects' gender, interventions, period of treatment, and outcome indicators of the included literatures were collected. A Meta-analysis was made of the data using Revman 5.3 software.Result: A total of 10 RCTs were included. The results of Meta-analysis showed that compared with the control group, the combined RR of clinical efficacy in the Plum Pill combined group was 1. 19,95% CI(1.11,1.26),with statistical significance(P < 0.05).The results of subgroup analysis showed that compared with the simple western medicine control group, the combined RR of clinical efficacy in the Plum Pill combined group was 1.18,95% CI(1.10,1.26),with statistical significance(P < 0.05).The heterogeneity test didn't show statistical significance. All studies of Plum Pill group had not been reported adverse reactions. Conclusion: Compared with the control group, Plum Pill had a better clinical efficacy and good safety, so it is suitable for clinical use.
引文
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