A randomized trial of short-course ciprofloxacin, ofloxacin, or trimethoprim/sulfamethoxazole for the treatment of acute urinary tract infection in women
Jm. Mccarthy et al., A randomized trial of short-course ciprofloxacin, ofloxacin, or trimethoprim/sulfamethoxazole for the treatment of acute urinary tract infection in women, AM J MED, 106(3), 1999, pp. 292-299
Citations number
20
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
PURPOSE: Bladder infections are very common in otherwise healthy women, and
short-course antimicrobial treatment appears effective for many episodes o
f cystitis. This study reports the results of short-course ciprofloxacin, o
floxacin, and trimethoprim/sulfamelhoxazole therapy.
PATIENTS AND METHODS: We performed a randomized, double-blind study of the
efficacy and safety of a 3-day course of oral ciprofloxacin 100 mg twice da
ily, ofloxacin 200 mg twice daily, or trimethoprim/sulfamethoxazole 160/800
mg twice daily in women with acute, uncomplicated, symptomatic lower urina
ry tract infection.
RESULTS: A total of 866 patients were enrolled, of whom 688 (79%) were eval
uated for the efficacy of treatment (229 treated with ciprofloxacin, 228 tr
eated with trimethoprim/suliamethoxazole, and 231 treated with ofloxacin).
The most frequent reason for exclusion was the failure to identify a pretre
atment pathogen. The most commonly isolated pathogen was Escherichia coli (
81%). Eradication of the pretreatment pathogen at the end of therapy occurr
ed in 94% of ciprofloxacin, 93% of trimethoprim/sulfamethoxazole, and 97% o
f ofloxacin-treated patients. At follow-up evaluation at 4 to 6 weeks, recu
rrence rates (relapse or reinfection) were 11% in the ciprofloxacin, 16% in
the trimethsprim/sulfamethoxazole, and 13% in the ofloxacin treatment grou
p. Clinical success at the end of therapy was 93% in the ciprofloxacin, 95%
in the trimethoprim/sulfamethoxazole, and 96% in the ofloxacin treatment g
roups. The frequency of all adverse events was 31% for ciprofloxacin, 41% f
or trimethoprim/sulfamethoxazole, and 39% for ofloxacin-treated patients (P
= 0.03). Premature discontinuation of study drug due to an adverse event w
as more common in trimethoprim/sulfamethoxazole-treated patients (n = 9) co
mpared with those given ciprofloxacin (n = 2) or ofloxacin (n = 1; P = 0.02
).
CONCLUSION: Ciprofloxacin, ofloxacin, and trimethoprim/sulfamethoxazole had
similar efficacy when given for 3 days to treat acute, symptomatic, uncomp
licated lower urinary tract infection in women. (C) 1999 by Excerpta Medica
, Inc.