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Utility of the Nonabsorbed (<0.4%) Antibiotic Rifaximin in Gastroenterology and Hepatology
Chinyu G Su1, Faten Aberra1, Gary R Lichtenstein1
1Dr. Su is Assistant Professor of Medicine, Dr. Aberra is Instructor in Medicine, and Dr. Lichtenstein is Professor of Medicine at the University of Pennsylvania School of Medicine in Philadelphia. Dr. Lichtenstein is also Director of the Center for Inflammatory Bowel Diseases at the Hospital of the University of Pennsylvania, Gastroenterology Division.
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.
Insights
Minimally absorbed oral antibiotics like rifaximin offer a safe and effective option for various enteric conditions, overcoming previous barriers to antibiotic use in gastroenterology. This reassessment highlights their growing therapeutic potential.
Area of Science:
- Gastroenterology and Hepatology
- Pharmacology
- Microbiology
Background:
- Oral antibiotics are underutilized in gastroenterology due to concerns about resistance, side effects, and drug interactions.
- Minimally absorbed oral antibiotics present a potential solution to mitigate these concerns.
- The introduction of rifaximin in 2004 marked a shift in the availability of such agents in the US.
Purpose of the Study:
- To reassess the therapeutic utility of minimally absorbed oral antibiotics, specifically rifaximin, for enteric conditions.
- To evaluate rifaximin's safety, efficacy, and potential role in gastroenterology and hepatology practice.
Main Methods:
- Review of in vitro data on rifaximin's antibacterial spectrum and gut-localized action.
- Analysis of clinical data supporting rifaximin's efficacy in various enteric conditions.
- Assessment of rifaximin's tolerability profile and drug interaction potential.
Main Results:
- Rifaximin demonstrates broad-spectrum activity against enteric pathogens with minimal systemic absorption.
- Established efficacy for infectious diarrhea and hepatic encephalopathy.
- Growing evidence supports its use in Crohn's disease, ulcerative colitis, small intestinal bacterial overgrowth, pouchitis, and antibiotic-associated colitis.
Conclusions:
- Rifaximin offers a favorable safety and tolerability profile, comparable to placebo, with no known drug interactions.
- Its gut-specific action makes it suitable for treating bacterial enteric infections and colonization.
- Further clinical studies and experience will define rifaximin's expanded role in gastroenterology and hepatology.
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