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Omeprazole-based triple therapy with low-versus high-dose of clarithromycin plus amoxicillin for H pylori eradication in Iranian population

机译:低剂量大剂量克拉霉素和阿莫西林为基础的奥美拉唑三联疗法在伊朗人群中根除幽门螺杆菌

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AIM: To investigate the efficacy and tolerability of H pylori eradication in an omeprazole-based triple therapy with high- and low-dose of clarithromycin and amoxicillin. METHODS: One hundred and sixty H pylori positive patients were randomly assigned to two groups based on the following 2 wk investigation; (1) group A or low-dose regimen received omeprazole 20 mg b.i.d, clarithromycin 250 mg b.i.d and amoxicillin 500 mg b.i.d; and (2) group B or high-dose regimen received omeprazole 20 mg b.i.d, clarithromycin 500 mg b.i.d and amoxicillin 1000 mg b.i.d. During the study H pylori status was assessed by histology and rapid urease test prior and by 13C-urea breath test 6 wk after the therapy. Standard questionnaires were administered to determine the compliance to treatment and possible adverse events of therapy. Data were subject to χ~2 to compare the eradication rates in the two groups. The significant level of 95% (P ≤ 0.05) was considered statistically different. RESULTS: We found that the per-protocol eradication rate was 88% (68/77) in group A, and 89% (67/75) in group B. The intension-to-treat eradication rate was 85% (68/80) in group A and 83.75% (67/80) in group B. Overall adverse events were 26% in group A and 31% in group B. The adverse events were generally mild in nature and tolerated well in both groups with a compliance of 98% in group A vs 96% in group B. CONCLUSION: The omeprazole-based low dose regimen of clarithromycin and amoxicillin for two weeks in H pylori eradication is as effective as high dose regimen in Iranian population.
机译:目的:研究在高剂量和低剂量克拉霉素和阿莫西林联合以奥美拉唑为基础的三联疗法中根除幽门螺杆菌的疗效和耐受性。方法:根据以下2周的调查,将160例幽门螺杆菌阳性患者随机分为两组。 (1)A组或小剂量方案接受奥美拉唑20 mg b.i.d,克拉霉素250 mg b.i.d和阿莫西林500 mg b.i.d; (2)B组或大剂量方案的奥美拉唑20 mg b.i.d,克拉霉素500 mg b.i.d和阿莫西林1000 mg b.i.d.在研究过程中,在治疗前和术后6周通过组织学和快速尿素酶测试以及通过13C-尿素呼气测试评估幽门螺杆菌状态。进行标准问卷调查以确定对治疗的依从性和可能的​​治疗不良事件。对数据进行χ〜2比较以比较两组的根除率。 95%的显着水平(P≤0.05)被认为具有统计学差异。结果:我们发现,A组的按协议根除率为88%(68/77),B组为89%(67/75)。从根治到根除的率为85%(68/80) A组中的A)和B组中的83.75%(67/80)。总体不良事件在A组中为26%,在B组中为31%。不良事件的性质一般较轻,并且两组患者的耐受性均良好结论:A组根除幽门螺杆菌的两周时间,基于奥美拉唑的克拉霉素和阿莫西林低剂量方案与高剂量方案一样有效,A组为98%,B组为96%。

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