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Rifabutin triple therapy for first-line and rescue treatment of Helicobacter pylori infection: A systematic review and meta-analysis.
Gingold-Belfer, Rachel; Niv, Yaron; Levi, Zohar; Boltin, Doron.
Afiliação
  • Gingold-Belfer R; Division of Gastroenterology, Rabin Medical Center, and the Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Niv Y; Division of Patient Safety and Quality Improvement, Ministry of Health, Jerusalem, Israel.
  • Levi Z; Division of Gastroenterology, Rabin Medical Center, and the Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Boltin D; Division of Gastroenterology, Rabin Medical Center, and the Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
J Gastroenterol Hepatol ; 36(6): 1392-1402, 2021 Jun.
Article em En | MEDLINE | ID: mdl-33037845
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, I2  = 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) (I2  = 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Helicobacter pylori / Infecções por Helicobacter / Rifabutina / Inibidores da Bomba de Prótons / Gastrite / Amoxicilina / Antibacterianos Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Helicobacter pylori / Infecções por Helicobacter / Rifabutina / Inibidores da Bomba de Prótons / Gastrite / Amoxicilina / Antibacterianos Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article