Neringer R, Forsgren A, Hansson C, Ode B
Department of Infectious Diseases Central Hospital, Karlskrona, Sweden.
Scand J Infect Dis. 1992;24(6):773-80. doi: 10.3109/00365549209062463.
This randomised, double-blind, multicenter study compared the safety and efficacy of lomefloxacin and norfloxacin in adult female outpatients with uncomplicated urinary tract infections. Patients were randomly assigned to one of 3 treatment groups: 400 mg lomefloxacin once daily for 3 days (L3), 400 mg lomefloxacin once daily for 7 days (L7), or 400 mg norfloxacin twice daily for 7 days (N7). A total of 703 patients (age 17-75 years) were enrolled at 21 investigative sites in southern Sweden. Clinical and microbiological evaluations were conducted at the start, 5-9 days and 3-4 weeks post therapy. Patients with quantitative urine cultures of > or = 10(4) CFU/ml of a susceptible pathogen were considered evaluable for efficacy. Escherichia coli and Staphylococcus saprophyticus were the most commonly isolated pathogens. In both L3 and L7 groups, 196 patients and in the N7 group 195 patients met the criteria for efficacy evaluation. At the 5-9 day post-treatment evaluation, 88% of the pathogens were eradicated in the L3 group, 93% in the L7 group and 93% in the N7 group. At the 3-4 week post-treatment evaluation, 81%, 82%, and 85% of urine cultures remained negative in the L3, L7, and N7 groups, respectively. No statistically significant differences between the 3 treatment groups were noted with the exception of eradication of S. saprophyticus, for which the 7 day courses were more effective at 4-9 days post treatment. No persistent pathogen developed resistance to the study drugs. All 3 treatment regimens were equally well tolerated, except for photosensitivity reactions, which were more frequently reported in patients in the lomefloxacin groups.
这项随机、双盲、多中心研究比较了洛美沙星和诺氟沙星在患有单纯性尿路感染的成年女性门诊患者中的安全性和有效性。患者被随机分配到3个治疗组之一:每日一次服用400mg洛美沙星,共3天(L3组);每日一次服用400mg洛美沙星,共7天(L7组);或每日两次服用400mg诺氟沙星,共7天(N7组)。瑞典南部的21个研究地点共招募了703名患者(年龄17 - 75岁)。在治疗开始时、治疗后5 - 9天和3 - 4周进行临床和微生物学评估。尿定量培养中易感性病原体≥10(4) CFU/ml的患者被认为可进行疗效评估。大肠埃希菌和腐生葡萄球菌是最常分离出的病原体。L3组和L7组各有196例患者,N7组有195例患者符合疗效评估标准。在治疗后5 - 9天的评估中,L3组88%的病原体被根除,L7组为93%,N7组为93%。在治疗后3 - 4周的评估中,L3组、L7组和N7组分别有81%、82%和85%的尿培养仍为阴性。除了腐生葡萄球菌的根除情况外,3个治疗组之间未发现统计学上的显著差异,对于腐生葡萄球菌,7天疗程在治疗后4 - 9天更有效。没有持续的病原体对研究药物产生耐药性。所有3种治疗方案的耐受性均良好,但洛美沙星组患者更频繁报告有光敏反应。