SHORT-COURSE CIPROFLOX TREATMENT OF ACUTE UNCOMPLICATED URINARY-TRACTINFECTION IN WOMEN - THE MINIMUM EFFECTIVE DOSE

Citation
A. Iravani et al., SHORT-COURSE CIPROFLOX TREATMENT OF ACUTE UNCOMPLICATED URINARY-TRACTINFECTION IN WOMEN - THE MINIMUM EFFECTIVE DOSE, Archives of internal medicine, 155(5), 1995, pp. 485-494
Citations number
28
Categorie Soggetti
Medicine, General & Internal
ISSN journal
00039926
Volume
155
Issue
5
Year of publication
1995
Pages
485 - 494
Database
ISI
SICI code
0003-9926(1995)155:5<485:SCTOAU>2.0.ZU;2-A
Abstract
Background: Three studies were undertaken to determine the minimum eff ective dosing regimen of ciprofloxacin for the treatment of acute, sym ptomatic, uncomplicated lower urinary tract infection. Methods: All st udies were multicenter, prospective, randomized, double-blind trials. A total of 970 evaluable patients with a diagnosis of urinary tract in fection received oral ciprofloxacin (200 mg to 500 mg daily in one or two divided doses for 1, 3, 5, or 7 days) or norfloxacin (400 mg twice daily [BID] for 7 days). The primary measure of efficacy was bacterio logic eradication at the end of therapy. Results: In study 1, bacterio logic eradication was reported in 95 (89%) and 101 (98%) of patients i n the groups who received ciprofloxacin, 500-mg single dose and 250 mg BID for 7 days, respectively. Clinical success occurred in 101 patien ts (94%) who received a 500-mg single dose and in 103 patients (100%) who were administered 250 mg BID for 7 days. In study 2, eradication r ates in the groups who received ciprofloxacin, 100 mg BID for 3 days, 250 mg BID for 3 days, and 250 mg BID for 7 days, were 98 (93%), 95 (9 0%), and 98 (93%), respectively. Clinical success was reported in 102 (97%), 105 (100%), and 104 (98%) of the patients, respectively. In stu dy 3, the eradication rates in the groups who received ciprofloxacin i n dosages of 500 mg once daily for 3 days and 500 mg once daily for 5 days and norfloxacin in a dosage of 400 mg BID for 7 days were 137 (92 %), 134 (90%), and 133 (94%) of the women, respectively. Clinical succ ess was the same (97%) in all three groups. Overall, short-course (eit her 3- or 5-day) therapy with ciprofloxacin was statistically equivale nt to conventional (7-day) therapy with either ciprofloxacin or norflo xacin. Single-dose ciprofloxacin therapy was statistically less effect ive than conventional treatment. Conclusions: Ciprofloxacin at a dosag e of 100 mg BID for 3 days was the minimum effective dose for the trea tment of uncomplicated urinary tract infection in women.