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Global eradication rates for Helicobacter pylori infection: systematic review and meta-analysis of sequential therapy

机译:幽门螺杆菌感染的全球根除率:序贯治疗的系统评价和荟萃分析

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摘要

>Objective To do a systematic review and meta-analysis of studies comparing sequential therapy for eradication of Helicobacter pylori with pre-existing and new therapies, thus providing a glimpse of eradication success worldwide.>Design Systematic review and meta-analysis.>Data sources Medline, Embase, and Cochrane Central Register of Controlled Trials up to May 2013; abstract books of major European, American, and Asian gastroenterological meetings.>Study selection Randomised controlled trials in previously untreated adults, in which sequential therapy was compared with a pre-existing or new therapy.>Results 46 randomised controlled trials were reviewed and analysed. 5666 patients were randomised to sequential therapy and 7866 to other (established and new) treatments. The overall eradication rate of sequential therapy was 84.3% (95% confidence interval 82.1% to 86.4%). Sequential therapy was superior to seven day triple therapy (relative risk 1.21, 95% confidence interval 1.17 to 1.25; I2=29.3%; number needed to treat 6 , 95% confidence interval 5% to 7%), marginally superior to 10 day triple therapy (1.11, 1.04 to 1.19; I2= 67.2%; NNT 10, 7 to 15), but not superior to 14 day triple therapy (1.00, 0.94 to 1.06; I2=54.3%), bismuth based therapy (1.01, 0.95 to 1.06; I2=21.1%), and non-bismuth based therapy (0.99, 0.94 to 1.05; I2=52.3%). Data on eradication according to pre-treatment antimicrobial susceptibility testing were available in eight studies, and sequential therapy was able to eradicate 72.8% (61.6% to 82.8%) of the strains resistant to clarithromycin.>Conclusions Eradication rates with pre-existing and new therapies for H pylori are suboptimal. Regional monitoring of resistance rates should help to guide treatment, and new agents for treatment need to be developed.
机译:>目的对进行根除幽门螺杆菌的序贯疗法与已有的和新的疗法进行比较的研究进行系统的回顾和荟萃分析,从而提供全球范围内根除成功的一瞥。>设计系统评价和荟萃分析。>数据来源:截至2013年5月的Medline,Embase和Cochrane对照试验中央注册; >研究选择在先前未治疗的成年人中进行的随机对照试验,其中将序贯治疗与既有治疗或新治疗进行了比较。>结果< / strong>审查并分析了46项随机对照试验。 5666例患者被随机分配至序贯治疗,7866例被随机分配至其他(既定和新的)治疗。序贯治疗的总根除率为84.3%(95%置信区间为82.1%至86.4%)。序贯治疗优于7天三联疗法(相对风险1.21,95%置信区间1.17至1.25; I 2 = 29.3%;治疗6所需的数字,95%置信区间5%至7% ),略优于10天三联疗法(1.11、1.04至1.19; I 2 = 67.2%; NNT 10、7至15),但不优于14天三联疗法(1.00、0.94至1.06; I 2 = 54.3%),基于铋的疗法(1.01、0.95至1.06; I 2 = 21.1%)和非基于铋的疗法(0.99、0.94)到1.05; I 2 = 52.3%)。八项研究均提供了根据治疗前药敏试验进行根除的数据,序贯疗法能够根除对克拉霉素有抗药性的菌株的72.8%(61.6%至82.8%)。>结论幽门螺杆菌的现有疗法和新疗法都不理想。耐药率的区域监测应有助于指导治疗,需要开发新的治疗药物。

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