Department of Infectious Diseases, University Medical Center Utrecht, Utrecht, The Netherlands.
Department of Julius Centre for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands.
Clin Infect Dis. 2022 Aug 25;75(2):221-229. doi: 10.1093/cid/ciab934.
We aimed to determine the noninferiority of fosfomycin compared to ciprofloxacin as an oral step-down treatment for Escherichia coli febrile urinary tract infections (fUTIs) in women.
This was a double-blind, randomized, controlled trial in 15 Dutch hospitals. Adult women who were receiving 2-5 days of empirical intravenous antimicrobials for E. coli fUTI were assigned to step-down treatment with once-daily 3g fosfomycin or twice-daily 0.5g ciprofloxacin for 10 days of total antibiotic treatment. For the primary end point, clinical cure at days 6-10 post-end of treatment (PET), a noninferiority margin of 10% was chosen. The trial was registered on Trialregister.nl (NTR6449).
After enrollment of 97 patients between 2017 and 2020, the trial ended prematurely because of the coronavirus disease 2019 pandemic. The primary end point was met in 36 of 48 patients (75.0%) assigned to fosfomycin and 30 of 46 patients (65.2%) assigned to ciprofloxacin (risk difference [RD], 9.6%; 95% confidence interval [CI]: -8.8% to 28.0%). In patients assigned to fosfomycin and ciprofloxacin, microbiological cure at days 6-10 PET occurred in 29 of 37 (78.4%) and 33 of 35 (94.3%; RD, -16.2%; 95% CI: -32.7 to -0.0%). Any gastrointestinal adverse event was reported in 25 of 48 (52.1%) and 14 of 46 (30.4%) patients (RD, 20.8%; 95% CI: 1.6% to 40.0%), respectively.
Fosfomycin is noninferior to ciprofloxacin as oral step-down treatment for fUTI caused by E. coli in women. Fosfomycin use is associated with more gastrointestinal events.
Trial NL6275 (NTR6449).
我们旨在确定磷霉素与环丙沙星相比,作为女性大肠埃希菌发热性尿路感染(fUTI)的口服降级治疗是否不劣于后者。
这是在 15 家荷兰医院进行的一项双盲、随机、对照试验。正在接受 2-5 天经验性静脉内抗菌药物治疗大肠埃希菌 fUTI 的成年女性被分配接受每日一次 3g 磷霉素或每日两次 0.5g 环丙沙星的 10 天抗生素总疗程的口服降级治疗。对于主要终点,即治疗结束后第 6-10 天(PET)的临床治愈率,选择了 10%的非劣效性边界。该试验在 Trialregister.nl(NTR6449)上注册。
在 2017 年至 2020 年间招募了 97 名患者后,由于 2019 年冠状病毒病(COVID-19)大流行,试验提前结束。48 名患者中,有 36 名(75.0%)分配到磷霉素组,46 名患者中有 30 名(65.2%)分配到环丙沙星组,主要终点达到(风险差[RD],9.6%;95%置信区间[CI]:-8.8%至 28.0%)。在接受磷霉素和环丙沙星治疗的患者中,PET 第 6-10 天的微生物学治愈率分别为 37 例中的 29 例(78.4%)和 35 例中的 33 例(94.3%;RD,-16.2%;95%CI:-32.7 至-0.0%)。分别有 48 名患者中的 25 名(52.1%)和 46 名患者中的 14 名(30.4%)报告有任何胃肠道不良事件(RD,20.8%;95%CI:1.6%至 40.0%)。
磷霉素作为女性大肠埃希菌 fUTI 的口服降级治疗不劣于环丙沙星。磷霉素的使用与更多的胃肠道事件相关。
NLR6275(NTR6449)。