Comparison of efficacies of dual therapy and triple therapy using rabeprazole in second-line eradication of Helicobacter pylori in Japan

T. KAWAI, K. KAWAKAMI, M. KATAOKA, S. TAIRA, T. ITOI, F. MORIYASU, Y. TAKAGI, T. AOKI, E. RIMBARA, N. NOGUCHI, M. SASATSU
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Abstract

Summary

Background

The only authorized second-line Helicobacter pylori regimen in Japan is proton pump inhibitor + amoxycillin + clarithromycin. However, it has been reported that this second-line regimen is not effective. In this study, we evaluated the efficacy of dual and triple eradication therapies using rabeprazole as second-line H. pylori eradication regimens.

Aim

To evaluate the efficacy of dual and triple eradication therapies using rabeprazole as second-line H. pylori eradication therapy.

Methods

Sixty-two H. pylori-positive patients with first-line eradication failure were randomly assigned to two groups. The RAM group was administered rabeprazole 20 mg + amoxycillin 1500 mg + metronidazole 500 mg daily for 1 week. The RA group was administered rabeprazole 40 mg + amoxycillin 2000 mg daily for 2 weeks. Eradication of H. pylori infection was determined by 13C-urea breath testing at 8 weeks after completion of treatment. Prior to treatment, amoxycillin, clarithromycin and metronidazole susceptibility, and CYP2C19 phenotype status were determined.

Results

Eradication rates for the RAM and RA groups were 97% and 74%, respectively. Eradication rates were not influenced by CYP2C19 phenotype in either group. Eradication rates for clarithromycin-resistant patients were 100% in the RAM group and 77% in the RA group.

Conclusions

One week with RAM therapy and 2 weeks with RA therapy were effective as second-line eradication therapy for H. pylori infection; moreover, RAM was more effective than RA therapy.

雷贝拉唑双联治疗与三联治疗在日本二线根除幽门螺杆菌的疗效比较
背景:日本唯一批准的幽门螺杆菌二线治疗方案是质子泵抑制剂+阿莫西林+克拉霉素。然而,据报道,这种二线方案是无效的。在这项研究中,我们评估了使用雷贝拉唑作为二线幽门螺杆菌根除方案的双重和三重根除疗法的疗效。目的评价雷贝拉唑作为幽门螺杆菌二线根除治疗的双重和三重治疗的疗效。方法将62例幽门螺杆菌阳性的一线根除失败患者随机分为两组。RAM组患者给予雷贝拉唑20 mg +阿莫西林1500 mg +甲硝唑500 mg,每日1周。RA组患者给予雷贝拉唑40 mg +阿莫西林2000 mg,每日2周。治疗结束后8周通过13c -尿素呼气试验检测幽门螺杆菌感染根除情况。治疗前检测患儿对阿莫西林、克拉霉素、甲硝唑的敏感性及CYP2C19表型状态。结果RAM组和RA组的根除率分别为97%和74%。两组的根除率均不受CYP2C19表型的影响。RAM组克拉霉素耐药患者的根除率为100%,RA组为77%。结论RAM治疗1周和RA治疗2周作为幽门螺杆菌感染的二线根除治疗有效;此外,RAM治疗比RA治疗更有效。
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