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