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Rifaximin dose-finding study for the treatment of small intestinal bacterial overgrowth
E C Lauritano1, M Gabrielli, A Lupascu
1Internal Medicine Department, Gemelli Hospital, Catholic University of Sacred Heart, Rome, Italy.
Background:
Few controlled studies assessing choice and duration of antibiotic therapy for small intestinal bacterial overgrowth are available.
Aim:
To assess efficacy, safety and tolerability of different doses of rifaximin, a broad spectrum non-absorbable antibiotic, for intestinal bacterial overgrowth eradication.
Methods:
We enrolled 90 consecutive patients affected by small intestinal bacterial overgrowth. The presence of small intestinal bacterial overgrowth was based on the occurrence of a rise of H2 values >12 p.p.m. above the basal value after 50 g glucose ingestion. Patients were randomized in three 7-day treatment groups: rifaximin 600 mg/day (group 1); rifaximin 800 mg/day (group 2) and rifaximin 1200 mg/day (group 3). Glucose breath test was reassessed 1 month after the end of therapy. Compliance to the treatment and incidence of side-effects were also evaluated.
Results:
No drop-outs were observed in the three groups. Glucose breath test normalization rate was significantly higher in group 3 (60%) with respect to group 1 (17%; P < 0.001) and group 2 (27%, P < 0.01). No significant differences in patient compliance and incidence of side-effects were found among groups.
Conclusions:
Higher doses of rifaximin lead to a significant gain in terms of therapeutic efficacy in small intestinal bacterial overgrowth eradication without increasing the incidence of side-effects.
Insights
Higher doses of rifaximin significantly improve small intestinal bacterial overgrowth eradication. This study found increased efficacy with higher rifaximin dosages without additional side effects, offering a better treatment option.
Area of Science:
- Gastroenterology
- Microbiology
- Pharmacology
Background:
- Limited controlled studies exist on antibiotic therapy for small intestinal bacterial overgrowth (SIBO).
- Investigating optimal antibiotic regimens for SIBO is crucial for effective patient management.
Purpose of the Study:
- To evaluate the efficacy, safety, and tolerability of varying rifaximin doses for SIBO eradication.
- Rifaximin, a non-absorbable antibiotic, was tested at different dosages.
Main Methods:
- 90 patients with SIBO were randomized into three groups receiving 7-day rifaximin treatments: 600 mg/day, 800 mg/day, or 1200 mg/day.
- SIBO diagnosis was confirmed via glucose breath test (H2 >12 p.p.m.).
- Efficacy was reassessed one month post-treatment using the glucose breath test; compliance and side effects were monitored.
Main Results:
- The highest rifaximin dose (1200 mg/day) showed a significantly higher SIBO eradication rate (60%) compared to lower doses (17% for 600 mg/day, 27% for 800 mg/day).
- No significant differences in treatment compliance or incidence of side effects were observed across the different dosage groups.
- All patients completed the study without drop-outs.
Conclusions:
- Higher doses of rifaximin demonstrate superior therapeutic efficacy in eradicating SIBO.
- Increasing rifaximin dosage for SIBO treatment enhances effectiveness without compromising safety or tolerability.
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