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A general practitioner multicenter study: fosfomycin trometamol single dose versus pipemidic acid multiple dose
1Department of Urology, Kremlin Bicentre Hospital, Paris, France.
Infection
|January 1, 1990
Summary
Fosfomycin trometamol offers effective and safe single-dose oral treatment for acute cystitis in women, showing comparable efficacy to pipemidic acid but with fewer, milder side effects. This makes it a convenient option for managing urinary tract infections.
Area of Science:
- Urology
- Infectious Diseases
- Pharmacology
Background:
- Acute cystitis is a common urinary tract infection in women.
- Current treatments often involve multi-day courses.
- Exploring single-dose antibiotic options can improve patient compliance and convenience.
Purpose of the Study:
- To evaluate the efficacy and safety of a single oral dose of fosfomycin trometamol.
- To compare fosfomycin trometamol with a standard five-day course of pipemidic acid for acute cystitis.
- To assess clinical and bacteriological outcomes at short-term and medium-term follow-up.
Main Methods:
- An open, multicenter comparative study in general practices.
- 386 women (16-75 years) with acute cystitis were enrolled.
- Treatment groups received either a single 3g dose of fosfomycin trometamol or pipemidic acid for five days.
- Diagnosis confirmed by clinical symptoms and significant bacteriuria (≥10^5 cfu/ml).
- Clinical and bacteriological evaluations at 5-10 days and 28 days post-treatment.
Main Results:
- Both treatments demonstrated comparable clinical and bacteriological efficacy.
- Short-term eradication rates: 122/146 (fosfomycin trometamol) vs. 130/143 (pipemidic acid).
- Medium-term eradication rates: 113/122 (fosfomycin trometamol) vs. 114/122 (pipemidic acid).
- Fosfomycin trometamol was associated with significantly milder and shorter-duration side effects.
Conclusions:
- Single-dose oral fosfomycin trometamol is an effective and well-tolerated treatment for acute cystitis in women.
- It presents a viable alternative to multi-day antibiotic regimens.
- The improved safety profile, particularly reduced side effect duration, enhances its therapeutic value.