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随机对照试验:药敏指导治疗与经验铋四联疗法治疗幽门螺杆菌一线治疗。

Randomised controlled trial: susceptibility-guided therapy versus empiric bismuth quadruple therapy for first-line Helicobacter pylori treatment.

机构信息

Shanghai, China.

Houston, Texas.

出版信息

Aliment Pharmacol Ther. 2019 Jun;49(11):1385-1394. doi: 10.1111/apt.15273. Epub 2019 Apr 24.

Abstract

BACKGROUND

Increasing Helicobacter pylori resistance has led to decreases in treatment effectiveness.

AIM

To test the effectiveness of susceptibility-guided therapy vs a locally highly effective empiric modified bismuth quadruple therapy for first-line H pylori treatment in a region with high antimicrobial resistance.

METHODS

We compared 14-day susceptibility-guided with empiric therapy using a multicentre superiority-design trial, which randomised H pylori infected subjects 3:1 to (a) susceptibility-guided therapies contained esomeprazole 20 mg and amoxicillin 1 g b.d. plus clarithromycin 500 mg, metronidazole 400 mg b.d., or levofloxacin 500 mg daily for susceptible infections or bismuth 220 mg b.d. and metronidazole 400 mg q.d.s. for triple-resistant infections; (b) Empiric therapy contained esomeprazole 20 mg, bismuth 220 mg b.d., amoxicillin 1 g and metronidazole 400 mg t.d.s. Primary outcome was H pylori eradication.

RESULTS

Between February 2017 and March 2018, 491 subjects were screened and 382 were randomised. Both the susceptibility-guided and the empiric regimens were highly successful with per-protocol eradication rates of 97.7% (250/256) vs 97.6% (81/83, P = 1.00) and intent-to-treat eradication rates of 91.6% (262/286) vs 85.4% (82/96, P = 0.12). Overall, susceptibility-guided therapy was not superior to empiric therapy with 0.1% per-protocol (95% CI -3.1% to 3.2%) and 6.2% intent-to-treat (-0.3% to 12.7%) eradication difference. Both approaches had high adherence and low adverse event rates.

CONCLUSIONS

Both susceptibility-guided and empiric therapies provided excellent eradication rates. Clinically, the choice would hinge on availability of susceptibility testing and/or a locally highly effective empiric therapy.

摘要

背景

幽门螺杆菌耐药率的上升导致治疗效果下降。

目的

在耐药率较高的地区,比较基于药敏试验的治疗方案与局部高度有效的经验性改良铋四联疗法作为一线治疗幽门螺杆菌感染的疗效。

方法

采用多中心优效性设计的临床试验,将幽门螺杆菌感染患者按 3:1 随机分组,分别接受 14 天的基于药敏试验的治疗或经验性治疗。在基于药敏试验的治疗组中,患者接受埃索美拉唑 20mg、阿莫西林 1g,每日 2 次,克拉霉素 500mg、甲硝唑 400mg,每日 2 次,或左氧氟沙星 500mg,每日 1 次,用于敏感感染;或铋剂 220mg,每日 2 次,甲硝唑 400mg,每日 4 次,用于三重耐药感染。经验性治疗组中,患者接受埃索美拉唑 20mg、铋剂 220mg,每日 2 次,阿莫西林 1g、甲硝唑 400mg,每日 3 次。主要终点为幽门螺杆菌根除率。

结果

2017 年 2 月至 2018 年 3 月期间,共筛选了 491 例患者,其中 382 例患者被随机分组。基于方案分析,基于药敏试验的治疗组和经验性治疗组的根除率分别为 97.7%(250/256)和 97.6%(81/83)(P=1.00),意向性治疗分析的根除率分别为 91.6%(262/286)和 85.4%(82/96)(P=0.12)。总体而言,基于药敏试验的治疗与经验性治疗相比,在基于方案分析(95%CI -3.1%至 3.2%)和意向性治疗分析(-0.3%至 12.7%)方面的根除率差异均为 0.1%。两种治疗方法的依从性均较高,不良事件发生率均较低。

结论

基于药敏试验的治疗和经验性治疗均可获得较高的根除率。在临床实践中,选择哪种治疗方法取决于药敏试验的可用性和/或当地高度有效的经验性治疗方案。

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