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利福布汀三联疗法作为幽门螺杆菌感染一线和补救治疗:系统评价和荟萃分析。

Rifabutin triple therapy for first-line and rescue treatment of Helicobacter pylori infection: A systematic review and meta-analysis.

机构信息

Division of Gastroenterology, Rabin Medical Center, and the Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Division of Patient Safety and Quality Improvement, Ministry of Health, Jerusalem, Israel.

出版信息

J Gastroenterol Hepatol. 2021 Jun;36(6):1392-1402. doi: 10.1111/jgh.15294. Epub 2020 Oct 29.

Abstract

BACKGROUND AND AIM

Due to the increasing resistance of Helicobacter pylori, there is a need for novel antibiotic treatment protocols. We aimed to perform a systematic review and meta-analysis in order to determine the effectiveness and safety of rifabutin triple therapy for H. pylori infection.

METHODS

We performed a systematic review of prospective clinical trials with a treatment arm consisting of proton pump inhibitor, amoxicillin, and rifabutin and a meta-analysis of randomized controlled trials (RCTs).

RESULTS

Thirty-three prospective studies including 44 datasets were identified. Meta-analysis of four RCTs for rescue treatment found no difference between treatment groups (odds ratio [OR] 0.88, 95% confidence interval [CI] 0.437-1.791, I  = 68.1%, P = 0.733). Only one RCT compared rifabutin therapy with control for first-line treatment of H. pylori infection (OR 3.78, 95% CI 2.44-5.87, P < 0.0001). Treatment was more likely to be successful in Asian versus non-Asian populations (81.0% vs 72.4%, P = 0.001) and when daily amoxicillin dose was ≥ 3000 mg or proton pump inhibitor dose was ≥ 80 mg or treatment duration was 14 days (80.6% vs 66.0%, P = 0.0001). The overall event rate for adverse effects was 24.8% (729/2937) (95% CI 0.23-0.26), and the pooled OR for adverse effects in the treatment versus control group was 0.93 (95% CI 0.50-1.75) (I  = 79.76, P = 0.82).

CONCLUSION

Evidence for the effectiveness of rifabutin for the first-line treatment of H. pylori infection in adults is limited, and studies comparing rifabutin with conventional first-line treatments are lacking.

摘要

背景与目的

由于幽门螺杆菌的耐药性不断增加,需要新的抗生素治疗方案。我们旨在进行系统评价和荟萃分析,以确定利福布汀三联疗法治疗幽门螺杆菌感染的有效性和安全性。

方法

我们对包含质子泵抑制剂、阿莫西林和利福布汀的治疗组的前瞻性临床试验进行了系统评价,并对随机对照试验(RCT)进行了荟萃分析。

结果

共确定了 33 项前瞻性研究,包含 44 个数据集。四项 RCT 用于挽救治疗的荟萃分析发现治疗组之间无差异(比值比 [OR] 0.88,95%置信区间 [CI] 0.437-1.791,I ² = 68.1%,P = 0.733)。仅有一项 RCT 比较了利福布汀治疗与对照用于幽门螺杆菌感染的一线治疗(OR 3.78,95%CI 2.44-5.87,P < 0.0001)。在亚洲人群中治疗更可能成功(81.0% vs 72.4%,P = 0.001),且当每日阿莫西林剂量≥3000mg 或质子泵抑制剂剂量≥80mg 或治疗持续时间为 14 天时(80.6% vs 66.0%,P = 0.0001)。不良事件的总发生率为 24.8%(729/2937)(95%CI 0.23-0.26),治疗组与对照组的不良事件发生率比值比(OR)为 0.93(95%CI 0.50-1.75)(I ² = 79.76,P = 0.82)。

结论

利福布汀作为成人幽门螺杆菌感染一线治疗的有效性证据有限,且缺乏将利福布汀与常规一线治疗进行比较的研究。

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