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二线抗幽门螺杆菌治疗的疗效:使用延长的 14 天左氧氟沙星/阿莫西林/质子泵抑制剂治疗——一项初步研究。

The efficacy of second-line anti-Helicobacter pylori therapy using an extended 14-day levofloxacin/amoxicillin/proton-pump inhibitor treatment--a pilot study.

机构信息

Division of Hepatogastroenterology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.

出版信息

Helicobacter. 2012 Oct;17(5):374-81. doi: 10.1111/j.1523-5378.2012.00960.x. Epub 2012 Jun 8.

Abstract

BACKGROUND

Large meta-analyses of second-line Helicobacter pylori eradication with fluoroquinolone triple therapy have shown that neither 7-day nor 10-day therapy provides 90% or better treatment success. Reports describing second-line H. pylori eradication using 14-day fluoroquinolone-containing triple therapy are few. Current study aimed to determine the efficacy of a 14-day levofloxacin/amoxicillin/proton-pump inhibitor regimen as second-line therapy and the clinical factors influencing the outcome.

MATERIALS AND METHODS

One-hundred and one patients who failed H. pylori eradication using the standard triple therapy for 7 days were randomly assigned to either a levofloxacin/amoxicillin/esomeprazole group (levofloxacin 500 mg once daily, amoxicillin 1 g twice daily, and esomeprazole 40 mg twice daily for 14 days) or a esomeprazole/metronidazole/bismuth salt/tetracycline group (esomeprazole 40 mg twice daily, metronidazole 250 mg four times daily, tripotassium dicitrate bismuthate 300 mg four times daily, and tetracycline 500 mg four times daily for 14 days). Follow-up to assess treatment response consisted of either endoscopy or a urea breath test, which were carried out 8 weeks later.

RESULTS

Eradication rates attained by levofloxacin/amoxicillin/esomeprazole and esomeprazole/metronidazole/bismuth salt/tetracycline treatments in the per-protocol analysis were 44/47 (93.6%; 95% CI = 86-99.8) and 43/47 (91.8%; 95% CI = 83.2-98.5). In the intention-to-treat analysis, these were 43/47 (86.3%; 95% CI = 76.5-96.1) in the LAE group (four lost to follow-up) and 43/50 (86%; 95% CI = 76-96) in the EMBT groups. The observed adverse events were 25.5% and 38.5% among the two groups. There was 100% drug compliance among the levofloxacin/amoxicillin/esomeprazole group. Levofloxacin-resistant strains occurred at a frequency of 32.3%. H. pylori eradication rates for the levofloxacin-susceptible strains and levofloxacin-resistant strains were 92% (11/12) and 33% (1/3) in the per-protocol analysis.

CONCLUSIONS

A 14-day levofloxacin/amoxicillin/esomeprazole triple therapy approach provides a >90% per-protocol report card with the caveat that this approach is markedly less effective in the presence of fluoroquinolone resistance. Levofloxacin-resistant strains are increasing in Taiwan.

摘要

背景

多项大型荟萃分析表明,二线含氟喹诺酮三联疗法根除幽门螺杆菌的治疗成功率均未达到 90%或以上,无论疗程为 7 天还是 10 天。目前,关于含氟喹诺酮 14 天三联疗法二线根除幽门螺杆菌的报道较少。本研究旨在确定 14 天左氧氟沙星/阿莫西林/质子泵抑制剂方案作为二线治疗的疗效,以及影响治疗效果的临床因素。

材料和方法

101 例患者经 7 天标准三联疗法治疗后未能根除幽门螺杆菌,随机分为左氧氟沙星/阿莫西林/埃索美拉唑组(左氧氟沙星 500mg 每日 1 次,阿莫西林 1g 每日 2 次,埃索美拉唑 40mg 每日 2 次,疗程 14 天)或埃索美拉唑/甲硝唑/铋盐/四环素组(埃索美拉唑 40mg 每日 2 次,甲硝唑 250mg 每日 4 次,枸橼酸铋钾 300mg 每日 4 次,四环素 500mg 每日 4 次,疗程 14 天)。通过内镜或尿素呼气试验进行随访以评估治疗反应,分别在 8 周后进行。

结果

在符合方案分析中,左氧氟沙星/阿莫西林/埃索美拉唑和埃索美拉唑/甲硝唑/铋盐/四环素治疗的根除率分别为 44/47(93.6%;95%可信区间=86-99.8)和 43/47(91.8%;95%可信区间=83.2-98.5)。在意向治疗分析中,LAE 组(4 例失访)的根除率为 43/47(86.3%;95%可信区间=76.5-96.1),EMBT 组的根除率为 43/50(86%;95%可信区间=76-96)。两组观察到的不良事件分别为 25.5%和 38.5%。左氧氟沙星/阿莫西林/埃索美拉唑组的药物依从性为 100%。左氧氟沙星耐药菌株的发生率为 32.3%。在符合方案分析中,左氧氟沙星敏感菌株和左氧氟沙星耐药菌株的根除率分别为 92%(11/12)和 33%(1/3)。

结论

14 天左氧氟沙星/阿莫西林/埃索美拉唑三联疗法的成功率>90%,但存在氟喹诺酮耐药时,该方案的疗效明显降低。在台湾,左氧氟沙星耐药菌株正在增加。

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