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首页> 外文期刊>Helicobacter >The Efficacy of Two-Week Quadruple First-Line Therapy with Bismuth, Lansoprazole, Amoxicillin, Clarithromycin on Helicobacter pylori Eradication: A Prospective Study
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The Efficacy of Two-Week Quadruple First-Line Therapy with Bismuth, Lansoprazole, Amoxicillin, Clarithromycin on Helicobacter pylori Eradication: A Prospective Study

机译:铋,兰索拉唑,阿莫西林,克拉霉素两周四联一线疗法对幽门螺杆菌根除的效果:前瞻性研究

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Aim: To document the efficacy and tolerability of 14-day bismuth–lansoprazole– amoxicillin–clarithromycin (BLAC) regimen for Helicobacter pylori (H. pylori) eradication as a first-line therapy. Method: Patients were considered eligible for the study if they underwent upper gastrointestinal endoscopy, and H. pylori infection was diagnosed through histologic examination of antral and body biopsy samples. Primary end point of this study was to evaluate the eradication rate of 14-day BLAC regimen therapies. H. pylori eradication was assessed using the 13C urea breath test performed 6 weeks after the completion of treatment. All patients were asked to fill in a validated questionnaire to report therapy-related side effects. Each symptom was graded from absent or present. Results: Ninety-seven (21 men and 76 women) were enrolled. All the patients completed the study. The H. pylori eradication rate was 90.7% (88 of 97 patients). Side effects were observed in reasonable percentages, and none of the patients left the study because of drug side effect. Conclusion: Bismuth–lansoprazole–amoxicillin–clarithromycin regimen as a 2-week course achieved an acceptable eradication rate with relatively mild side effects.
机译:目的:记录14天铋-兰索拉唑-阿莫西林-克拉霉素(BLAC)方案作为一线治疗幽门螺杆菌(H. pylori)的疗效和耐受性。方法:如果患者接受了上消化道内窥镜检查,则认为该患者符合研究条件,并且通过对肛门和身体活检样本进行组织学检查诊断为幽门螺杆菌感染。这项研究的主要目的是评估14天BLAC疗法的根除率。治疗结束后6周,使用13C尿素呼气试验评估幽门螺杆菌的根除情况。要求所有患者填写经过验证的问卷以报告与治疗相关的副作用。每种症状从不存在或存在到分级。结果:招募了97名(21名男性和76名女性)。所有患者均完成了研究。幽门螺杆菌的根除率为90.7%(97例患者中的88例)。以合理的百分比观察到了副作用,并且没有患者因药物副作用而退出研究。结论:铋-兰索拉唑-阿莫西林-克拉霉素治疗方案为期2周,根除率较高,且副作用相对较轻。

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