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Comparative study of esomeprazole and lansoprazole in triple therapy for eradication of Helicobacter pylori in Japan

机译:日本埃索美拉唑和兰索拉唑三联疗法根除幽门螺杆菌的比较研究

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摘要

AIM: To evaluate the efficacy and safety of esomeprazole-based triple therapy compared with lansoprazole therapy as first-line eradication therapy for patients with Helicobacter pylori (H. pylori) in usual post-marketing use in Japan, where the clarithromycin (CAM) resistance rate is 30%.METHODS: For this multicenter, randomized, open-label, non-inferiority trial, we recruited patients (≥ 20 years of age) with H. pylori infection from 20 hospitals in Japan. We randomly allocated patients to esomeprazole therapy (esomeprazole 20 mg, CAM 400 mg, amoxicillin (AC) 750 mg for the first 7 d, with all drugs given twice daily) or lansoprazole therapy (lansoprazole 30 mg, CAM 400 mg, AC 750 mg for the first 7 d, with all drugs given twice daily) using a minimization method with age, sex, and institution as adjustment factors. Our primary outcome was the eradication rate by intention-to-treat (ITT) and per-protocol (PP) analyses. H. pylori eradication was confirmed by a urea breath test from 4 to 8 wk after cessation of therapy.RESULTS: ITT analysis revealed the eradication rates of 69.4% (95%CI: 61.2%-76.6%) for esomeprazole therapy and 73.9% (95%CI: 65.9%-80.6%) for lansoprazole therapy (P = 0.4982). PP analysis showed eradication rate of 76.9% (95%CI: 68.6%-83.5%) for esomeprazole therapy and 79.8% (95%CI: 71.9%-86.0%) for lansoprazole therapy (P = 0.6423). There were no differences in adverse effects between the two therapies.CONCLUSION: Esomeprazole showed non-inferiority and safety in a 7 day-triple therapy for eradication of H. pylori compared with lansoprazole.
机译:目的:评估以埃索美拉唑为基础的三联疗法与兰索拉唑疗法作为根除一线治疗幽门螺杆菌(H. pylori)患者在一线常规上市后使用中对克拉霉素(CAM)耐药的日本患者的疗效和安全性比率为30%。方法:对于这项多中心,随机,开放标签,非自卑性试验,我们从日本的20家医院招募了幽门螺杆菌感染的患者(≥20岁)。我们将患者随机分配到埃索美拉唑治疗(前7天为esomeprazole 20 mg,CAM 400 mg,阿莫西林(AC)750 mg,所有药物每天两次)或lansoprazole治疗(lansoprazole 30 mg,CAM 400 mg,AC 750 mg)在头7天中,所有药物每天服用两次),采用最小化方法,将年龄,性别和机构作为调整因素。我们的主要结果是通过意图治疗(ITT)和按方案(PP)分析的根除率。停止治疗后4到8周,通过尿素呼气试验证实了幽门螺杆菌的根除。结果:ITT分析显示,埃索美拉唑治疗的根除率为69.4%(95%CI:61.2%-76.6%),而根除率为73.9%(95%CI:61.2%-76.6%)。兰索拉唑治疗的95%CI:65.9%-80.6%(P = 0.4982)。 PP分析显示,埃索美拉唑治疗的根除率为76.9%(95%CI:68.6%-83.5%),兰索拉唑治疗的根除率为79.8%(95%CI:71.9%-86.0%)(P = 0.6423)。结论:埃索美拉唑与兰索拉唑相比,在消灭幽门螺杆菌的7天三联疗法中,埃索美拉唑显示出非劣效性和安全性。

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