Literature DB >> 28286448

Utility of the Nonabsorbed (<0.4%) Antibiotic Rifaximin in Gastroenterology and Hepatology.

Chinyu G Su1, Faten Aberra1, Gary R Lichtenstein1.   

Abstract

Oral antibiotics have probable or documented therapeutic utility for multiple enteric conditions commonly treated by gastroenterologists and hepatologists, but they are not frequently prescribed. Barriers to antibiotic use include concerns about bacterial resistance, drug interactions, and antibiotic-associated side effects and toxicity, particularly in vulnerable populations. The use of minimally absorbed oral antibiotics has been suggested as an approach to overcoming some of these barriers, but minimally absorbed antibiotics have not been an important part of the US gastroenterologists' or hepatologists' armamentarium until recently. The 2004 introduction in the United States of the nonabsorbed (<0.4%) oral antibiotic rifaximin is cause for reassessing the potential usefulness of minimally absorbed oral antibiotics for bacterial enteric illness. Rifaximin has broad-spectrum in vitro antibacterial activity against enteric pathogens, gut-localized action, and minimal systemic absorption-a profile consistent with usefulness for a range of enteric conditions involving a pathogenetic role of bacteria. The emerging clinical profile of rifaximin also supports its potential utility for multiple enteric conditions. Rifaximin has a tolerability profile comparable to that of placebo and is not known to interact clinically with other medications. The efficacy of rifaximin is well documented for the treatment of infectious diarrhea caused by noninvasive pathogens and hepatic encephalopathy. A growing body of data supports the efficacy of rifaximin for additional enteric conditions, such as Crohn's disease, ulcerative colitis, small-intestinal bacterial overgrowth, pouchitis, and antibiotic-associated colitis, that are characterized by acute bacterial infection or bacterial colonization. In addition, rifaximin has recently been demonstrated effective in the prevention of travelers' diarrhea and shigellosis in controlled clinical studies. Ongoing studies and more experience with rifaximin in clinical practice will help to further define the role of this antibiotic in gastroenterology and hepatology.

Entities:  

Keywords:  Rifaximin; antibiotic; minimally absorbed

Year:  2006        PMID: 28286448      PMCID: PMC5335639     

Source DB:  PubMed          Journal:  Gastroenterol Hepatol (N Y)        ISSN: 1554-7914


  55 in total

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Journal:  Gastroenterol Clin North Am       Date:  2002-03       Impact factor: 3.806

3.  Comparison of rifaximin and lactitol in the treatment of acute hepatic encephalopathy: results of a randomized, double-blind, double-dummy, controlled clinical trial.

Authors:  Antoni Mas; Juan Rodés; Lourdes Sunyer; Luís Rodrigo; Ramon Planas; Victor Vargas; Lluís Castells; Dolores Rodríguez-Martínez; Conrado Fernández-Rodríguez; Ignasi Coll; Albert Pardo
Journal:  J Hepatol       Date:  2003-01       Impact factor: 25.083

4.  Antibiotic combination therapy in patients with chronic, treatment-resistant pouchitis.

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Journal:  Aliment Pharmacol Ther       Date:  1999-06       Impact factor: 8.171

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Authors:  David B Huang; Herbert L DuPont
Journal:  J Infect       Date:  2005-02       Impact factor: 6.072

6.  Clinical effects of rifaximin in patientswith hepatic encephalopathy intolerant or nonresponsive to previous lactulose treatment: An open-label, pilot study.

Authors:  Claudia Sama; Antonio Maria Morselli-Labate; Paolo Pianta; Laura Lambertini; Sonia Berardi; Gabriella Martini
Journal:  Curr Ther Res Clin Exp       Date:  2004-09

Review 7.  Rifaximin: in vitro and in vivo antibacterial activity--a review.

Authors:  Z D Jiang; H L DuPont
Journal:  Chemotherapy       Date:  2005       Impact factor: 2.544

8.  Rifaximin in the treatment of chronic hepatic encephalopathy.

Authors:  A Puxeddu; M Quartini; A Massimetti; A Ferrieri
Journal:  Curr Med Res Opin       Date:  1995       Impact factor: 2.580

9.  Rifaximin versus neomycin on hyperammoniemia in chronic portal systemic encephalopathy of cirrhotics. A double-blind, randomized trial.

Authors:  G Pedretti; C Calzetti; G Missale; F Fiaccadori
Journal:  Ital J Gastroenterol       Date:  1991-05

10.  CXC and CC chemokine expression in inflamed and noninflamed pelvic ileal pouch tissue.

Authors:  Ulf Helwig; Paolo Gionchetti; Fernando Rizzello; Karen Lammers; Tanja Kühbacher; Stefan Schreiber; Marco Baggiolini; Mariagrazia Uguccioni; Massimo Campieri
Journal:  Int J Colorectal Dis       Date:  2003-06-25       Impact factor: 2.571

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