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Itopride therapy for functional dyspepsia: A meta-analysis

机译:依托必利治疗功能性消化不良的荟萃分析

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摘要

AIM: To evaluate the therapeutic effects of itopride vs other drugs (placebo, domperidone, mosapride) for functional dyspepsia (FD).METHODS: Randomized controlled trials (RCTs) of itopride for FD were retrieved from databases. Relevant information was extracted and analyzed, using the relative risk (RR) and weighted mean deviation, as appropriate. A random or fixed effect model was used, based on the heterogeneity of the included articles, and visual inspection of funnel plots was used to evaluate publication bias.RESULTS: Nine RCTs enrolling 2620 FD cases were included; 1372 cases received itopride treatment and 1248 cases received placebo or other drugs (control groups). Compared with control groups, itopride had superior RR values of 1.11 [95%CI: (1.03, 1.19), P = 0.006], 1.21 [95%CI: (1.03, 1.44), P = 0.02], and 1.24 [95%CI: (1.01, 1.53), P = 0.04] for global patient assessment, postprandial fullness, and early satiety, respectively. For the Leeds Dyspepsia Questionnaire score, the weighted mean deviation was -1.38 [95%CI: (-1.75, -1.01), P < 0.01]. The incidence of adverse effects was similar in the itopride and control groups. The funnel plots for all indicators showed no evidence of publication bias.CONCLUSION: Itopride has good efficacy in terms of global patients assessment, postprandial fullness, and early satiety in the treatment of patients with FD and shows a low rate of adverse reactions. Itopride can greatly improve FD syndromes-score.
机译:目的:评估伊托必利与其他药物(安慰剂,多潘立酮,莫沙必利)对功能性消化不良(FD)的治疗效果。方法:从数据库中检索伊托必利用于FD的随机对照试验(RCT)。适当地使用相对风险(RR)和加权平均偏差来提取和分析相关信息。基于纳入文章的异质性,使用随机或固定效应模型,并通过漏斗图的目视检查来评估发表偏倚。结果:纳入了9例RCT,共纳入2620例FD病例。接受伊托必利治疗的患者为1372例,接受安慰剂或其他药物的患者为1248例(对照组)。与对照组相比,伊托必利具有较高的RR值,分别为1.11 [95%CI:(1.03,1.19),P = 0.006],1.21 [95%CI:(1.03,1.44),P = 0.02]和1.24 [95% CI:(1.01,1.53),P = 0.04]分别用于总体患者评估,餐后饱腹感和早期饱腹感。对于利兹消化不良调查问卷评分,加权平均偏差为-1.38 [95%CI:(-1.75,-1.01),P <0.01]。在伊托必利和对照组中,不良反应的发生率相似。结论:依托必利在整体患者评估,餐后饱腹感和早期饱腹感方面对FD患者具有良好的疗效,不良反应发生率低。依托必利可大大改善FD综合征评分。

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