The Effect of a Nonabsorbed Oral Antibiotic (Rifaximin) on the Symptoms of the Irritable Bowel Syndrome
A Randomized Trial
- Mark Pimentel, MD;
- Sandy Park, BA;
- James Mirocha;
- Sunanda V. Kane, MD; and
- Yuthana Kong, MPH
- From the Cedars-Sinai Medical Center, Burns and Allen Research Institute, and University of California, Los Angeles, Geffen School of Medicine, Los Angeles, California, and University of Chicago, Chicago, Illinois.
Abstract
Background: Alterations in gut flora may be important in the pathophysiology of the irritable bowel syndrome (IBS).
Objective: To determine whether the nonabsorbed antibiotic rifaximin is more effective than placebo in reducing symptoms in adults with IBS.
Design: Double-blind, randomized, placebo-controlled study.
Setting: 2 tertiary care medical centers.
Participants: 87 patients who met Rome I criteria for IBS and were enrolled from December 2003 to March 2005.
Interventions: Participants who met enrollment criteria were randomly assigned to receive 400 mg of rifaximin 3 times daily for 10 days (n = 43) or placebo (n = 44). Eighty participants completed rifaximin therapy or placebo, and follow-up data were available for at least 34 participants per study group at any time point thereafter.
Measurements: A questionnaire was administered before treatment and 7 days after treatment. The primary outcome was global improvement in IBS. Patients were then asked to keep a weekly symptom diary for 10 weeks.
Results: Over the 10 weeks of follow-up, rifaximin resulted in greater improvement in IBS symptoms (P = 0.020). In addition, rifaximin recipients had a lower bloating score after treatment.
Limitations: The major limitations of the study were its modest sample size and short duration and that most patients were from 1 center.
Conclusions: Rifaximin improves IBS symptoms for up to 10 weeks after the discontinuation of therapy.
Article and Author Information
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Acknowledgments: The authors thank Tess Constantino, RN, and Vicki Lees-Kim, RN, for their assistance with patient coordination; Robert Wade for his vast experience with lactulose breath testing; and Dr. Soumya Chatterjee for his assistance in auditing the data. In addition, they thank the Beatrice and Samuel A. Seaver Foundation, which has been a gracious supporter of the work on gut bacteria and IBS.
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Grant Support: By Salix Pharmaceuticals.
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Potential Financial Conflicts of Interest:Consultancies: M. Pimentel (Novartis, Chugai Pharmaceutical, Promethus, Romark, Salix Pharmaceuticals); Honoraria: M. Pimentel (Novartis, Salix Pharmaceuticals); Grants received: M. Pimentel (Salix Pharmaceuticals); Patents received: M. Pimentel (Cedars-Sinai Medical Center); Patents pending: M. Pimentel (Cedars-Sinai Medical Center). Cedars-Sinai Medical Center has a licensing agreement with Salix Pharmaceuticals.
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Request for Single Reprints: Mark Pimentel, MD, Cedars-Sinai Medical Center, 8730 Alden Drive, Suite 225E, Los Angeles, CA, 90048; e-mail, pimentelm{at}cshs.org.
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Current Author Addresses: Dr. Pimentel, Ms. Park, and Ms. Kong: Cedars-Sinai Medical Center, 8730 Alden Drive, Suite 225E, Los Angeles, CA 90048.
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Dr. Mirocha: Biostatistics Core, Research Institute and General Clinical Research Center and Cardiothoracic Surgery, Cedars-Sinai Medical Center, Room 101, Atrium Annex Building, 8700 Beverly Boulevard, Los Angeles, CA 90048.
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Dr. Kane: University of Chicago, 5841 South Maryland Avenue, MC 4076, Chicago, IL 60637.
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Author Contributions: Conception and design: M. Pimentel, S. Park, Y. Kong.
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Analysis and interpretation of the data: M. Pimentel, J. Mirocha.
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Drafting of the article: M. Pimentel, S. Park, S.V. Kane.
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Critical revision of the article for important intellectual content: M. Pimentel, S. Park, J. Mirocha, S.V. Kane, Y. Kong.
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Final approval of the article: M. Pimentel, J. Mirocha, Y. Kong.
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Provision of study materials or patients: M. Pimentel, S.V. Kane.
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Statistical expertise: M. Pimentel, J. Mirocha.
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Obtaining of funding: M. Pimentel.
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Administrative, technical, or logistic support: M. Pimentel, S. Park, Y. Kong.
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Collection and assembly of data: M. Pimentel, S. Park, Y. Kong.
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ClinicalTrials.gov Identifier: NCT00259155.
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