5天联合治疗成功根除幽门螺杆菌

GastroHep Pub Date : 2022-06-16 DOI:10.1155/2022/1211329
L. Goldberg, Thomas J. Amrick
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引用次数: 0

摘要

背景。未经治疗的幽门螺杆菌与胃肠道疾病有关,包括消化性溃疡疾病、慢性胃炎和胃癌。ACG指南目前要求三联治疗,包括PPI、克拉霉素、阿莫西林或甲硝唑,持续14天。ACG建议将这种治疗作为一线治疗,尽管认识到对克拉霉素的耐药性日益增加,目前高达15-20%。目标研究了5天伴随根除方案的有效性。方法。这是一项回顾性研究,77名幽门螺杆菌感染,治疗naïve患者,在我们的新泽西州社区环境中,给予5天的联合治疗,包括左氧氟沙星500毫克,阿莫西林1毫克,替硝唑500毫克,埃索美拉唑40毫克。C13尿素呼气试验证实根除。结果。在我们对65例患者的意向治疗分析中,54例患者(83.03%)通过C13尿素呼气试验证实根除。结论。在社区实践中,5天的联合治疗(左氧氟沙星、埃索美拉唑、替硝唑和阿莫西林)可达到80-90%的高效根除率。与ACG共识指南中推荐的更长10 - 14天治疗相比,我们的治疗方案达到了相当的清除率,如果不是更好的话。此外,我们的方案使患者依从性更好,更具成本效益,时间更短,甚至与新疗法(如利法布汀)相比耐受性良好。因此,这些结果成功地证明,这种最初于20多年前确定的5天b.i.d.治疗仍然是一种有效的选择,并且可能优于传统的10 - 14天治疗,因为它具有相当的清除率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful Eradication of Helicobacter pylori with 5-Day Concomitant Treatment
Background. Untreated Helicobacter pylori is associated with gastrointestinal conditions including peptic ulcer disease, chronic gastritis, and gastric cancer. The ACG guidelines presently call for triple therapy consisting of a PPI, clarithromycin, and amoxicillin or metronidazole for 14 days. The ACG recommends this treatment as a first-line therapy despite the recognition of growing resistance to clarithromycin, presently upwards of 15-20%. Aims. Studied was the effectiveness of a 5-day concomitant eradication protocol. Methods. This was a retrospective study of 77 H. pylori infected, treatment naïve patients, prescribed a 5-day concomitant therapy containing levofloxacin 500 mg b.i.d., amoxicillin 1 gm b.i.d., tinidazole 500 mg b.i.d., and esomeprazole 40 mg b.i.d. in our New Jersey community setting. Eradication was confirmed with C13 urea breath test. Results. In our intention-to-treat analysis of 65 patients, 54 patients (83.03%) achieved eradication confirmed by C13 urea breath testing. Conclusions. Highly efficacious eradication rates of 80-90% can be achieved with 5-day concomitant treatment (levofloxacin, esomeprazole, tinidazole, and amoxicillin) in a community practice. Our treatment protocol achieves comparable, if not better, clearance rates as compared to agents specified in the ACG consensus guidelines recommending a longer 10–14-day treatment. Additionally, our protocol resulted in better patient compliance, was more cost-effective, shorter, and was well-tolerated compared even to newer treatments, like rifabutin. Thus, these results successfully demonstrate that this 5-day b.i.d. therapy, originally identified over 20 years ago, continues to be an effective choice option and is likely superior as it has comparable clearance rates to traditional 10–14-day therapy.
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