Treatment success for Helicobacter pylori, a major human pathogen, with popular drug regimens has generally declined to unacceptably low levels. As part of the worldwide effort to identify novel drug regimens that will reliably achieve high levels of success, Tay, Marshall and colleagues report their results with novel multidrug-tailored therapies.
This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Fibrinogen production is enhanced in an in-vitro model of non-alcoholic fatty liver disease: an isolated risk factor for cardiovascular events?
Lipids in Health and Disease Open Access 10 August 2015
Access options
Subscribe to this journal
Receive 12 print issues and online access
$189.00 per year
only $15.75 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Tay, C. Y. et al. Helicobacter pylori eradication in Western Australia using novel quadruple therapy combinations. Aliment. Pharmacol. Ther. http://dx.doi.org/10.1111/apt.12089.
Rimbara, E., Fischbach, L. A. & Graham, D. Y. Optimal therapy for Helicobacter pylori infections. Nat. Rev. Gastroenterol. Hepatol. 8, 79–88 (2011).
Graham, D. Y. & Lu, H. Furazolidone in Helicobacter pylori therapy: misunderstood and often unfairly maligned drug told in a story of French bread. Saudi J. Gastroenterol. 18, 1–2 (2012).
Fischbach, L. A., van, Z. S. & Dickason, J. Meta-analysis: the efficacy, adverse events, and adherence related to first-line anti-Helicobacter pylori quadruple therapies. Aliment. Pharmacol. Ther. 20, 1071–1082 (2004).
Borody, T. J. et al. Efficacy and safety of rifabutin-containing 'rescue therapy' for resistant Helicobacter pylori infection. Aliment. Pharmacol. Ther. 23, 481–488 (2006).
Federico, A. et al. Efficacy of 5-day levofloxacin-based concomitant therapy in eradication of Helicobacter pylori infection. Gastroenterology 143, 55–61 (2012).
Hsu, P. I., Wu, D. C., Wu, J. Y. & Graham, D. Y. Modified sequential Helicobacter pylori therapy: proton pump inhibitor and amoxicillin for 14 days with clarithromycin and metronidazole added as a quadruple (Hybrid) therapy for the final 7 days. Helicobacter 16, 139–145 (2011).
Uygun, A. et al. Efficacy of a modified sequential therapy including bismuth subcitrate as first-line therapy to eradicate Helicobacter pylori in a Turkish population. Helicobacter 17, 486–490 (2012).
Saad, R. J., Schoenfeld, P., Kim, H. M. & Chey, W. D. Levofloxacin-based triple therapy versus bismuth-based quadruple therapy for persistent Helicobacter pylori infection: a meta-analysis. Am. J. Gastroenterol. 101, 488–496 (2006).
Gisbert, J. P. & Morena, F. Systematic review and meta-analysis: levofloxacin-based rescue regimens after Helicobacter pylori treatment failure. Aliment. Pharmacol. Ther. 23, 35–44 (2006).
Acknowledgements
Dr. Graham is supported in part by the Office of Research and Development Medical Research Service Department of Veterans Affairs, Public Health Service grant DK56338, which funds the Texas Medical Center Digestive Diseases Center, DK067366 and CA116845. The contents of this article are solely the responsibility of the authors and do not necessarily represent the official views of the Veterans Affairs or NIH.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
Dr. Graham is a unpaid consultant for Novartis in relation to vaccine development for treatment or prevention of H. pylori infection. Dr. Graham is also a paid consultant for RedHill Biopharma regarding novel H. pylori therapies and for Otsuka Pharmaceuticals regarding diagnostic testing. Dr. Graham has received royalties from Baylor College of Medicine patents covering materials related to 13C-urea breath test. Dr. Gisbert has served as a speaker, a consultant and advisory member for, or has received research funding from Almirall, Janssen-Cilag, Nycomed, and AstraZeneca.
Rights and permissions
About this article
Cite this article
Graham, D., Gisbert, J. Tailored therapy with novel sequential quadruple therapies. Nat Rev Gastroenterol Hepatol 10, 6–8 (2013). https://doi.org/10.1038/nrgastro.2012.232
Published:
Issue date:
DOI: https://doi.org/10.1038/nrgastro.2012.232
This article is cited by
-
Fibrinogen production is enhanced in an in-vitro model of non-alcoholic fatty liver disease: an isolated risk factor for cardiovascular events?
Lipids in Health and Disease (2015)