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在社区和医院人群中根除幽门螺杆菌方面,10天序贯疗法与14天三联疗法的对比:一项随机试验。

Sequential therapy for 10 days versus triple therapy for 14 days in the eradication of in the community and hospital populations: a randomised trial.

作者信息

Liou Jyh-Ming, Chen Chieh-Chang, Chang Chi-Yang, Chen Mei-Jyh, Chen Chien-Chuan, Fang Yu-Jen, Lee Ji-Yuh, Yang Tsung-Hua, Luo Jiing-Chyuan, Wu Jeng-Yih, Liou Tai-Cherng, Chang Wen-Hsiung, Hsu Yao-Chun, Tseng Cheng-Hao, Chang Chun-Chao, Bair Ming-Jong, Liu Tzeng-Ying, Hsieh Chun-Fu, Tsao Feng-Yun, Shun Chia-Tung, Lin Jaw-Town, Lee Yi-Chia, Wu Ming-Shiang

机构信息

Departments of Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.

Department of Internal Medicine, E-DA Hospital and I-Shou University, Kaohsiung County, Taiwan.

出版信息

Gut. 2016 Nov;65(11):1784-1792. doi: 10.1136/gutjnl-2015-310142. Epub 2015 Sep 3.

Abstract

OBJECTIVE

Significant heterogeneity was observed in previous trials that assessed the efficacies of sequential therapy for 10 days (S10) versus triple therapy for 14 days (T14) in the first-line treatment of We aimed to compare the efficacy of S10 and T14 and assess the factors affecting their efficacies.

DESIGN

We conducted this open-label randomised multicentre trial in eight hospitals and one community in Taiwan. 1300 adult subjects with infection naïve to treatment were randomised (1:1) to receive S10 (lansoprazole and amoxicillin for the first 5 days, followed by lansoprazole, clarithromycin and metronidazole for another 5 days) or T14 (lansoprazole, amoxicillin and clarithromycin for 14 days). All drugs were given twice daily. Successful eradication was defined as negative C-urea breath test at least 6 weeks after treatment. Our primary outcome was the eradication rate by intention-to-treat (ITT) and per-protocol (PP) analyses. Antibiotic resistance was determined by agar dilution test.

RESULTS

The eradication rates of S10 and T14 were 87.2% (567/650, 95% CI 84.4% to 89.6%) and 85.7% (557/650, 95% CI 82.8% to 88.2%) in the ITT analysis, respectively, and were 91.6% (556/607, 95% CI 89.1% to 93.4%) and 91.0% (548/602, 95% CI 88.5% to 93.1%) in the PP analysis, respectively. There were no differences in compliance or adverse effects. The eradication rates in strains susceptible and resistant to clarithromycin were 90.7% and 62.2%, respectively, for S10, and were 91.5% and 44.4%, respectively, for T14. The efficacy of T14, but not S10, was affected by CYP2C19 polymorphism.

CONCLUSIONS

S10 was not superior to T14 in areas with low clarithromycin resistance.

TRIAL REGISTRATION NUMBER

NCT01607918.

摘要

目的

在先前评估一线治疗中10天序贯疗法(S10)与14天三联疗法(T14)疗效的试验中观察到显著的异质性。我们旨在比较S10和T14的疗效,并评估影响其疗效的因素。

设计

我们在台湾的八家医院和一个社区进行了这项开放标签随机多中心试验。1300名初治的成年感染患者被随机(1:1)分为接受S10(前5天服用兰索拉唑和阿莫西林,后5天服用兰索拉唑、克拉霉素和甲硝唑)或T14(14天服用兰索拉唑、阿莫西林和克拉霉素)。所有药物均每日服用两次。成功根除定义为治疗后至少6周C-尿素呼气试验阴性。我们的主要结局是意向性分析(ITT)和符合方案分析(PP)的根除率。通过琼脂稀释试验确定抗生素耐药性。

结果

ITT分析中,S10和T14的根除率分别为87.2%(567/650,95%CI 84.4%至89.6%)和85.7%(557/650,95%CI 82.8%至88.2%),PP分析中分别为91.6%(556/607,95%CI 89.1%至93.4%)和91.0%(548/602,95%CI 88.5%至93.1%)。依从性或不良反应方面无差异。对克拉霉素敏感和耐药菌株的S10根除率分别为90.7%和62.2%,T14分别为91.5%和44.4%。T14的疗效受CYP2C19多态性影响,而S10不受影响。

结论

在克拉霉素耐药率较低的地区,S10并不优于T14。

试验注册号

NCT01607918。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe2/5099199/9dbb2024a936/gutjnl-2015-310142f01.jpg

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