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Sitafloxacin for Third-Line Helicobacter pylori Eradication: A Systematic Review

Background and Aim: Sitafloxacin-based therapy is a potent candidate for third-line Helicobacter pylori eradication treatment. In this systematic review, we summarise current reports with sitafloxacin-based therapy as a third-line treatment. Methods: Clinical studies were systematically searched usi...

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Autores principales: Nishizawa, Toshihiro, Munkjargal, Munkhbayar, Ebinuma, Hirotoshi, Toyoshima, Osamu, Suzuki, Hidekazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234224/
https://www.ncbi.nlm.nih.gov/pubmed/34202993
http://dx.doi.org/10.3390/jcm10122722
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author Nishizawa, Toshihiro
Munkjargal, Munkhbayar
Ebinuma, Hirotoshi
Toyoshima, Osamu
Suzuki, Hidekazu
author_facet Nishizawa, Toshihiro
Munkjargal, Munkhbayar
Ebinuma, Hirotoshi
Toyoshima, Osamu
Suzuki, Hidekazu
author_sort Nishizawa, Toshihiro
collection PubMed
description Background and Aim: Sitafloxacin-based therapy is a potent candidate for third-line Helicobacter pylori eradication treatment. In this systematic review, we summarise current reports with sitafloxacin-based therapy as a third-line treatment. Methods: Clinical studies were systematically searched using PubMed, Cochrane library, Web of Science, and the Igaku-Chuo-Zasshi database. We combined data from clinical studies using a random-effects model and calculated pooled event rates, 95% confidence intervals (CIs), and the pooled odds ratio (OR). Results: We included twelve clinical studies in the present systematic review. The mean eradication rate for 7-day regimens of either PPI (proton pump inhibitor) or vonoprazan–sitafloxacin–amoxicillin was 80.6% (95% CI, 75.2–85.0). The vonoprazan–sitafloxacin–amoxicillin regimen was significantly superior to the PPI–sitafloxacin–amoxicillin regimen (pooled OR of successful eradication: 6.00; 95% CI: 2.25–15.98, p < 0.001). The PPI–sitafloxacin–amoxicillin regimen was comparable with PPI–sitafloxacin–metronidazole regimens (pooled OR: 1.06; 95% CI: 0.55–2.07, p = 0.86). Conclusions: Although the 7-day regimen composed of vonoprazan, sitafloxacin, and amoxicillin is a good option as the third-line Helicobacter pylori eradication treatment in Japan, the extension of treatment duration should be considered to further improve the eradication rate. Considering the safety concern of fluoroquinolones, sitafloxcin should be used after confirming drug susceptibility.
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spelling pubmed-82342242021-06-27 Sitafloxacin for Third-Line Helicobacter pylori Eradication: A Systematic Review Nishizawa, Toshihiro Munkjargal, Munkhbayar Ebinuma, Hirotoshi Toyoshima, Osamu Suzuki, Hidekazu J Clin Med Review Background and Aim: Sitafloxacin-based therapy is a potent candidate for third-line Helicobacter pylori eradication treatment. In this systematic review, we summarise current reports with sitafloxacin-based therapy as a third-line treatment. Methods: Clinical studies were systematically searched using PubMed, Cochrane library, Web of Science, and the Igaku-Chuo-Zasshi database. We combined data from clinical studies using a random-effects model and calculated pooled event rates, 95% confidence intervals (CIs), and the pooled odds ratio (OR). Results: We included twelve clinical studies in the present systematic review. The mean eradication rate for 7-day regimens of either PPI (proton pump inhibitor) or vonoprazan–sitafloxacin–amoxicillin was 80.6% (95% CI, 75.2–85.0). The vonoprazan–sitafloxacin–amoxicillin regimen was significantly superior to the PPI–sitafloxacin–amoxicillin regimen (pooled OR of successful eradication: 6.00; 95% CI: 2.25–15.98, p < 0.001). The PPI–sitafloxacin–amoxicillin regimen was comparable with PPI–sitafloxacin–metronidazole regimens (pooled OR: 1.06; 95% CI: 0.55–2.07, p = 0.86). Conclusions: Although the 7-day regimen composed of vonoprazan, sitafloxacin, and amoxicillin is a good option as the third-line Helicobacter pylori eradication treatment in Japan, the extension of treatment duration should be considered to further improve the eradication rate. Considering the safety concern of fluoroquinolones, sitafloxcin should be used after confirming drug susceptibility. MDPI 2021-06-20 /pmc/articles/PMC8234224/ /pubmed/34202993 http://dx.doi.org/10.3390/jcm10122722 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Nishizawa, Toshihiro
Munkjargal, Munkhbayar
Ebinuma, Hirotoshi
Toyoshima, Osamu
Suzuki, Hidekazu
Sitafloxacin for Third-Line Helicobacter pylori Eradication: A Systematic Review
title Sitafloxacin for Third-Line Helicobacter pylori Eradication: A Systematic Review
title_full Sitafloxacin for Third-Line Helicobacter pylori Eradication: A Systematic Review
title_fullStr Sitafloxacin for Third-Line Helicobacter pylori Eradication: A Systematic Review
title_full_unstemmed Sitafloxacin for Third-Line Helicobacter pylori Eradication: A Systematic Review
title_short Sitafloxacin for Third-Line Helicobacter pylori Eradication: A Systematic Review
title_sort sitafloxacin for third-line helicobacter pylori eradication: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234224/
https://www.ncbi.nlm.nih.gov/pubmed/34202993
http://dx.doi.org/10.3390/jcm10122722
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