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根除治疗的混合方案与联合方案比较:一项随机临床试验

A Comparison between Hybrid and Concomitant Regimens for Eradication: A Randomized Clinical Trial.

作者信息

Alhooei Saman, Tirgar Fakheri Hafez, Hosseini Vahid, Maleki Iradj, Taghvaei Tarang, Valizadeh Seyed Mohammad, Bari Zohreh

机构信息

Assistant Professor, Department of Gastroenterology, Golestan University of Medical Sciences, Gorgan, Iran.

Professor, Department of Gastroenterology, Gut and Liver Research Center, Mazandaran University of Medical Sciences, Sari, Iran.

出版信息

Middle East J Dig Dis. 2016 Jul;8(3):219-225. doi: 10.15171/mejdd.2016.24.

DOI:10.15171/mejdd.2016.24
PMID:27698972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5045675/
Abstract

BACKGROUND is one of the most common bacterial infections worldwide. We designed a study to compare the efficacy of 14-day hybrid regimen with 10-day concomitant therapy for eradication in Iran. METHODS 252 patients with naïve infection were randomly divided to receive either hybrid regimen (pantoprazole 40 mg, and amoxicillin 1 gr twice daily for 14 days, accompanied by clarithromycin 500 mg, and metronidazole 500 mg, twice daily just during the last 7 days) or concomitant regimen (pantoprazole 40 mg, amoxicillin 1 gr, clarithromycin 500 mg, and metronidazole 500 mg, all twice daily for 10 days). 8 weeks after therapy, C- urease breath test was performed to confirm eradication. RESULTS According to intention to treat analysis, the eradication rates were 87.3% (95% CI: 81.4-93.1) and 80.9% (95% CI: 74-87.8) in hybrid and concomitant groups, respectively (=0.38). Per-protocol eradication rates were 89.3% (95% CI: 83.8-94.7) and 83.1% (95% CI: 76.3-89.8), respectively (=0.19). The rates of severe side effects were not statistically different between the two groups (4% vs. 8.7%). CONCLUSION 14-day hybrid therapy can be considered as a nearly acceptable regimen with few severe side effects in Iran. However, it seems that the efficacy of this therapy is decreasing as the resistance rates to antibiotics are increasing. We suggest further studies to assess the efficacy of a more prolonged concomitant therapy for eradication in Iran.

摘要

背景 是全球最常见的细菌感染之一。我们设计了一项研究,以比较14天混合疗法与10天联合疗法在伊朗根除 的疗效。方法 将252例初治 感染患者随机分为两组,分别接受混合疗法(泮托拉唑40毫克,阿莫西林1克,每日两次,共14天,仅在最后7天加用克拉霉素500毫克和甲硝唑500毫克,每日两次)或联合疗法(泮托拉唑40毫克,阿莫西林1克,克拉霉素500毫克,甲硝唑500毫克,均每日两次,共10天)。治疗8周后,进行C尿素呼气试验以确认根除情况。结果 根据意向性分析,混合组和联合组的根除率分别为87.3%(95%CI:81.4 - 93.1)和80.9%(95%CI:74 - 87.8)( =0.38)。符合方案分析的根除率分别为89.3%(95%CI:83.8 - 94.7)和83.1%(95%CI:76.3 - 89.8)( =0.19)。两组严重副作用发生率无统计学差异(4%对8.7%)。结论 在伊朗,14天混合疗法可被视为一种几乎可接受的方案,严重副作用较少。然而,随着抗生素耐药率的增加,这种疗法的疗效似乎在下降。我们建议进一步研究以评估在伊朗延长联合疗法根除 的疗效。 (注:原文中“BACKGROUND”后及“ERADICATION”前应补充具体疾病名称,这里按原文直接翻译,可能影响理解)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038b/5045675/e8a0a1b1f295/mejdd-8-219-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038b/5045675/e8a0a1b1f295/mejdd-8-219-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038b/5045675/e8a0a1b1f295/mejdd-8-219-g001.jpg

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