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两种含左氧氟沙星的二线治疗方案对幽门螺杆菌的疗效:一项初步研究。

Efficacy of two levofloxacin-containing second-line therapies for Helicobacter pylori: a pilot study.

机构信息

Department of Gastroenterology, Umraniye Training and Research Hospital, Istanbul, Turkey.

出版信息

Helicobacter. 2013 Oct;18(5):378-83. doi: 10.1111/hel.12056. Epub 2013 Apr 21.

Abstract

BACKGROUND

An ideal second-line therapeutic regimen for the treatment of patients who do not respond to standard triple therapy is currently being investigated. In this study, we aimed to investigate the efficacy of two levofloxacin-containing second-line therapies for Helicobacter pylori (H. pylori).

MATERIALS AND METHODS

One hundred and forty eight consecutive H. pylori -positive patients who did not respond to the standard triple therapy (77 female, 71 male) were enrolled in the study. The patients were randomized consecutively to two-second-line therapy groups; 73 to the levofloxacin-containing sequential (LCS) and 75 to the levofloxacin-containing quadruple (LCQ) therapy group. The LCS therapy group received pantoprazole 40 mg and amoxicillin 1,000 mg twice daily for 5 days followed by pantoprazole 40 mg twice daily and metronidazole 500 mg three times daily and levofloxacin 500 mg one time daily for 7 days. The LCQ therapy group received pantoprazole 40 mg twice daily, tetracycline 500 mg four times daily, bismuth subcitrate 300 mg four times daily and levofloxacin 500 mg one time daily for 10 days. H. pylori eradication was confirmed by stool antigen testing at least 6 weeks after cessation of therapy. Side-effects and compliance were assessed by a questionnaire.

RESULTS

Intention-to-treat cure rates were: 82.2% (95%CI; 73-91) and 90.6% (95%CI; 79-95) in the LCS and LCQ therapy, respectively. Per protocol cure rates were: 85.7% (95%CI; 75-92) and 93.1% (95%CI; 85-98) in the LCS and LCQ therapy, respectively. No statistically significant difference was found between two groups (p = .1). No differences in compliance or adverse effects were demonstrated between two groups.

CONCLUSIONS

This prospective trial demonstrates that both levofloxacin-containing sequential therapy and levofloxacin-containing quadruple therapy regimens have higher H. pylori eradication rates and are well tolerated. The levofloxacin-containing quadruple therapy is likely the best treatment option for a second-line therapy, at least in the Turkish population.

摘要

背景

目前正在研究一种用于治疗对标准三联疗法无反应的患者的理想二线治疗方案。在这项研究中,我们旨在研究两种含左氧氟沙星的二线疗法对幽门螺杆菌(H. pylori)的疗效。

材料和方法

148 例连续的 H. pylori 阳性患者对标准三联疗法无反应(77 名女性,71 名男性)入组本研究。患者连续随机分为二线治疗两组;73 例为含左氧氟沙星序贯治疗(LCS)组,75 例为含左氧氟沙星四联治疗(LCQ)组。LCS 治疗组给予泮托拉唑 40mg 和阿莫西林 1000mg,每日 2 次,连用 5 天,随后给予泮托拉唑 40mg,每日 2 次,甲硝唑 500mg,每日 3 次,左氧氟沙星 500mg,每日 1 次,连用 7 天。LCQ 治疗组给予泮托拉唑 40mg,每日 2 次,四环素 500mg,每日 4 次,枸橼酸铋钾 300mg,每日 4 次,左氧氟沙星 500mg,每日 1 次,连用 10 天。停药至少 6 周后通过粪便抗原检测确认 H. pylori 根除。通过问卷调查评估副作用和依从性。

结果

意向治疗治愈率分别为:LCS 治疗组 82.2%(95%CI;73-91)和 LCQ 治疗组 90.6%(95%CI;79-95)。按方案治愈率分别为:LCS 治疗组 85.7%(95%CI;75-92)和 LCQ 治疗组 93.1%(95%CI;85-98)。两组间无统计学差异(p=0.1)。两组间的依从性或不良反应无差异。

结论

这项前瞻性试验表明,含左氧氟沙星的序贯疗法和含左氧氟沙星的四联疗法均具有较高的 H. pylori 根除率,且耐受性良好。含左氧氟沙星的四联疗法可能是二线治疗的最佳选择,至少在土耳其人群中如此。

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