Frankenschmidt A, Naber K G, Bischoff W, Kullmann K
Department of Urology, University Hospital, Freiburg, Germany.
J Urol. 1997 Oct;158(4):1494-9.
We compared the efficacy and safety of once-daily fleroxacin and twice-daily ciprofloxacin in patients with complicated urinary tract infections.
Using a prospective, open, randomized, multicenter study design, 133 patients (67 fleroxacin, 66 ciprofloxacin) were treated with doses of either 200 mg. of fleroxacin once daily or 250 mg. of ciprofloxacin twice daily in phase 1. In phase 2, 211 patients (103 fleroxacin, 108 ciprofloxacin) received 400 mg. of fleroxacin once daily or 500 mg. of ciprofloxacin twice a day.
In phase 1, bacteriological efficacy was excellent only against sensitive pathogens, such as Escherichia coli (84% with fleroxacin, 88% with ciprofloxacin), but high failure rates were observed in infections caused by Pseudomonas species (56% with fleroxacin, 67% with ciprofloxacin) and gram-positive organisms (52% with fleroxacin, 67% with ciprofloxacin). In phase 2, bacteriological overall success rate was 88% in the fleroxacin group and 84% in the ciprofloxacin group. Clinical overall success was observed in more than 90% of patients in both groups (94% with fleroxacin, 93% with ciprofloxacin). No statistically significant differences between the drugs were observed in efficacy during phase 2, including a 4 to-6-week followup. Tolerance was also similar for fleroxacin and ciprofloxacin, with about 20% of patients reporting adverse events.
The results suggest that both fleroxacin and ciprofloxacin are safe and effective for the treatment of complicated urinary tract infections at the higher doses used in phase 2, with fleroxacin offering the advantage of a once-daily dosing regimen. Lower doses of fleroxacin (200 mg. once daily) should only be used to treat urinary tract infections caused by gram-negative organisms with minimum inhibiting concentrations of less than 0.5 mg./l.
我们比较了每日一次氟罗沙星和每日两次环丙沙星治疗复杂性尿路感染患者的疗效和安全性。
采用前瞻性、开放性、随机、多中心研究设计,133例患者(67例氟罗沙星,66例环丙沙星)在第一阶段接受每日200mg氟罗沙星或每日两次250mg环丙沙星治疗。在第二阶段,211例患者(103例氟罗沙星,108例环丙沙星)接受每日400mg氟罗沙星或每日两次500mg环丙沙星治疗。
在第一阶段,仅对敏感病原体如大肠杆菌的细菌学疗效良好(氟罗沙星为84%,环丙沙星为88%),但在由假单胞菌属和革兰氏阳性菌引起的感染中观察到高失败率(氟罗沙星为56%,环丙沙星为67%;氟罗沙星为52%,环丙沙星为67%)。在第二阶段,氟罗沙星组细菌学总体成功率为88%,环丙沙星组为84%。两组超过90%的患者获得临床总体成功(氟罗沙星为94%,环丙沙星为93%)。在第二阶段包括4至6周随访期间,两种药物在疗效方面未观察到统计学显著差异。氟罗沙星和环丙沙星的耐受性也相似,约20%的患者报告有不良事件。
结果表明,在第二阶段使用的较高剂量下,氟罗沙星和环丙沙星治疗复杂性尿路感染均安全有效,氟罗沙星具有每日一次给药方案的优势。较低剂量的氟罗沙星(每日200mg)仅应用于治疗由最低抑菌浓度小于0.5mg/l的革兰氏阴性菌引起的尿路感染。