Abstract |
This prospective, randomized controlled study compared the efficacy and safety of ciprofloxacin alone versus a conventional two- drug regimen, clindamycin with gentamicin. The study group included 71 patients hospitalized for pelvic infections such as acute (N = 33) and chronic (N = 8) salpingitis, tubo-ovarian abscesses (N = 11), endometritis (N = 9), septic abortion (N = 3), and other categories (N = 7). Twenty-two of 35 patients on ciprofloxacin and 20 of 36 on clindamycin plus gentamicin had culturable pathogens: gonococci in 28, anaerobes in six, chlamydia in four, and associated pathogens in 19. Complete clinical and bacteriologic cure was achieved in 21 of 22 (95%) in the ciprofloxacin group and 19 of 20 (95%) in the clindamycin plus gentamicin group. The mean duration of intravenous/oral ciprofloxacin therapy was 3.7/7.2 days, and it was 3/6.6 days for clindamycin plus gentamicin. Ciprofloxacin, a new quinolone, appears to be safe as a single- drug therapy and was as effective as the combination of clindamycin plus gentamicin for the treatment of severe pelvic infections requiring hospitalization.
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Authors | H Thadepalli, D Mathai, R Scotti, M B Bansal, E Savage |
Journal | Obstetrics and gynecology
(Obstet Gynecol)
Vol. 78
Issue 4
Pg. 696-702
(Oct 1991)
ISSN: 0029-7844 [Print] United States |
PMID | 1923175
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Gentamicins
- Clindamycin
- Ciprofloxacin
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Topics |
- Acute Disease
- Adolescent
- Adult
- Ciprofloxacin
(therapeutic use)
- Clindamycin
(administration & dosage, therapeutic use)
- Drug Therapy, Combination
- Female
- Gentamicins
(administration & dosage, therapeutic use)
- Humans
- Pelvic Inflammatory Disease
(drug therapy, microbiology)
- Prospective Studies
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