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Seven-day quintuple regimen as a rescue therapy for Helicobacter pylori eradication

机译:七天五倍方案作为幽门螺杆菌根除的抢救疗法

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摘要

AIM: To determine the efficacy of two quintuple regimens for eradication of Helicobacter pylori (H. pylori) in patients who failed previous therapies.METHODS: This prospective, open-label, randomized controlled trial was a phase II study conducted from April 2011 to March 2012 at the Gastrointestinal and Liver Diseases Research Center in Rasht, Iran. A total of 208 patients with dyspepsia who failed previous H. pylori eradication with a ten-day quadruple therapy were enrolled. A random block method was used to assign patients to one of two treatment groups. Patients in the first group were treated with 240 mg bismuth subcitrate, 20 mg omeprazole, 1000 mg amoxicillin, 500 mg clarithromycin and 500 mg tinidazole (BOACT group). Patients in the second group received a regimen containing 240 mg bismuth subcitrate, 20 mg omeprazole, 500 mg tetracycline, 500 mg metronidazole and 200 mg ofloxacin (BOTMO group). Both regimens were given twice daily for a duration of seven days. The eradication was confirmed by a 14C urea breath test 12 wk after completion of therapy. Patient compliance and drug side effects were evaluated at the end of the treatment period. The success rates were calculated by intention-to-treat and per-protocol analyses.RESULTS: A total of 205 patients completed the course of treatment, with three patients excluded due to drug intolerance. The mean age of patients did not differ between the BOACT and BOTMO groups (41.6 ± 12.2 years vs 39.6 ± 11.8 years), and no significant differences were found between the two groups in terms of age, sex, smoking habits or the initial eradication regimen. The intention-to-treat and per-protocol eradication rates were significantly higher in the BOTMO group (86.5%, 95%CI: 0.85-0.87 and 86.7%, 95%CI: 0.80-0.89, respectively) compared with the BOACT group (75.5%, 95%CI: 0.73-0.76 and 76%, 95%CI: 0.69-0.80, respectively) (P < 0.05). Univariate analyses for both groups did not show any association of sex, smoking and initial therapeutic regimen with eradiation rate (P > 0.05 for all). Significantly more patients experienced side effects in the BOACT group compared to the BOTMO group (77.4% vs 36.6%, P < 0.01). This difference was exemplified by increases in headache and taste disturbance (P < 0.05).CONCLUSION: Quintuple therapy with a BOTMO regimen is an alternative second-line rescue therapy for Iranian patients with failed first-line eradication treatment of H. pylori.
机译:目的:确定两种五联疗法在先前治疗失败的患者中根除幽门螺杆菌(H. pylori)的疗效。方法:这项前瞻性,开放标签,随机对照试验是一项于2011年4月至3月进行的II期研究。 2012年在伊朗拉什特的胃肠道和肝脏疾病研究中心。共有208位消化不良的患者接受了为期10天的四联疗法而根除先前的幽门螺杆菌失败。使用随机阻断法将患者分配到两个治疗组之一。第一组患者接受240毫克柠檬酸铋,20毫克奥美拉唑,1000毫克阿莫西林,500毫克克拉霉素和500毫克替硝唑治疗(BOACT组)。第二组患者接受的治疗方案包括240 mg柠檬酸铋,20 mg奥美拉唑,500 mg四环素,500 mg甲硝唑和200 mg氧氟沙星(BOTMO组)。两种方案每天两次,持续7天。治疗结束后12周通过 14 C尿素呼气试验证实了根除。在治疗期结束时评估患者的依从性和药物副作用。结果:通过意向性治疗和按方案分析计算出成功率。结果:共有205例患者完成了治疗过程,其中3例患者由于药物耐受性而被排除在外。 BOACT组和BOTMO组之间的患者平均年龄没有差异(41.6±12.2岁vs 39.6±11.8岁),并且两组在年龄,性别,吸烟习惯或初始根除方案方面均无显着差异。与BOACT组相比,BOTMO组的意向治疗和根除方案的比率显着更高(分别为86.5%,95%CI:0.85-0.87和86.7%,95%CI:0.80-0.89)( 75.5%,95%CI:0.73-0.76和76%,95%CI:0.69-0.80)(P <0.05)。两组的单因素分析均未显示性别,吸烟和初始治疗方案与放射率之间有任何关联(所有P> 0.05)。与BOTMO组相比,BOACT组中有更多的患者出现了副作用(77.4%比36.6%,P <0.01)。结论:头痛和味觉障碍的增加说明了这种差异(P <0.05)。结论:对于一线根除幽门螺杆菌失败的伊朗患者,BOTMO方案进行五联疗法是另一种二线抢救疗法。

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