Effect of an individualized bismuth quadruple regimen guided by 10-day or 14-day antibiotic susceptibility testing for first-line eradication treatment of Helicobacter pylori in Ningxia, China.

IF 3.1 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Frontiers in Medicine Pub Date : 2025-01-10 eCollection Date: 2024-01-01 DOI:10.3389/fmed.2024.1510376
Xiaoming Su, Yanhong Deng, Xianmei Chen, Yanling Li, Qian Hao, Yuanyuan Tang, Rui Mu, Yuting Wu, Yan Zhou, Shengjuan Hu
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Abstract

Introduction: Helicobacter pylori (H. pylori) is becoming more resistant to antibiotics, and the implementation of individualized therapy is highly valuable for its eradication. This study aimed to investigate the efficacy and safety of individualized treatment guided by antibiotic susceptibility testing (AST) with a 10-day or 14-day course for the eradication of H. pylori.

Methods: This was a prospective, open-label, single-center, quasi-randomized trial in which 220 participants were randomized into groups based on AST results as AST-10-day (n = 98) and AST-14-day (n = 112) treatment groups. All participants were retested for a 14-carbon urease breath test at weeks 4-8 after the end of the treatment.

Results: The primary resistance rates of H. pylori to metronidazole, levofloxacin, clarithromycin, and amoxicillin were 94.1% (207/220), 42.7% (95/220), 41.4% (91/220), and 0.9% (2/220), respectively; however, no resistance to furazolidone and tetracycline was observed. In the AST-10-day and AST-14-day groups, the intention-to-treat (ITT) eradication rates were 89.8% (88/98) and 90.2% (110/122), respectively, with no statistically significant difference (p = 0.928). The per-protocol (PP) eradication rates were 92.6% (88/95) and 98.2% (110/112), respectively, with a statistically significant difference (p = 0.049). The incidence rates of adverse events (AEs) in the AST-10-day and AST-14-day groups were 6.3% (6/95) and 7.2% (8/112), respectively, with no statistically significant difference (p = 0.813). No statistically significant difference was observed in compliance between the two groups (p = 0.467).

Conclusion: Both 10-day and 14-day AST guided individualized therapy can achieve satisfactory eradication effect. Compared with the 14-day regimen, the 10-day regimen has similar eradication rate and incidence of adverse events and compliance but shorter duration and lower cost.

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以10天或14天抗生素药敏试验为指导的个体化四联铋治疗方案在中国宁夏幽门螺杆菌一线根除治疗中的效果
导读:幽门螺杆菌(Helicobacter pylori, H. pylori)对抗生素的耐药性越来越强,实施个体化治疗对其根除具有重要意义。本研究旨在探讨以抗生素药敏试验(AST)为指导的个体化治疗10天或14天疗程根除幽门螺杆菌的有效性和安全性。方法:这是一项前瞻性、开放标签、单中心、准随机试验,220名参与者根据AST结果随机分为AST-10天(n = 98)和AST-14天(n = 112)治疗组。在治疗结束后的第4-8周,所有参与者都重新进行了14碳脲酶呼吸测试。结果:幽门螺旋杆菌对甲硝唑、左氧氟沙星、克拉霉素、阿莫西林的一次耐药率分别为94.1%(207/220)、42.7%(95/220)、41.4%(91/220)、0.9% (2/220);但未见对呋喃唑酮和四环素的耐药性。ast -10 d组和ast -14 d组的ITT根除率分别为89.8%(88/98)和90.2%(110/122),差异无统计学意义(p = 0.928)。每方案(PP)根除率分别为92.6%(88/95)和98.2%(110/112),差异有统计学意义(p = 0.049)。ast -10天组不良事件(ae)发生率为6.3% (6/95),ast -14天组不良事件发生率为7.2%(8/112),差异无统计学意义(p = 0.813)。两组依从性比较差异无统计学意义(p = 0.467)。结论:10天和14天AST引导个体化治疗均可取得满意的根除效果。与14天方案相比,10天方案的根除率、不良事件发生率和依从性相似,但持续时间更短,成本更低。
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来源期刊
Frontiers in Medicine
Frontiers in Medicine Medicine-General Medicine
CiteScore
5.10
自引率
5.10%
发文量
3710
审稿时长
12 weeks
期刊介绍: Frontiers in Medicine publishes rigorously peer-reviewed research linking basic research to clinical practice and patient care, as well as translating scientific advances into new therapies and diagnostic tools. Led by an outstanding Editorial Board of international experts, this multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. In addition to papers that provide a link between basic research and clinical practice, a particular emphasis is given to studies that are directly relevant to patient care. In this spirit, the journal publishes the latest research results and medical knowledge that facilitate the translation of scientific advances into new therapies or diagnostic tools. The full listing of the Specialty Sections represented by Frontiers in Medicine is as listed below. As well as the established medical disciplines, Frontiers in Medicine is launching new sections that together will facilitate - the use of patient-reported outcomes under real world conditions - the exploitation of big data and the use of novel information and communication tools in the assessment of new medicines - the scientific bases for guidelines and decisions from regulatory authorities - access to medicinal products and medical devices worldwide - addressing the grand health challenges around the world
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