Rodríguez-Gómez Jorge, Gracia-Ahufinger I Irene, Carmona-Flores Rosario, Guzmán-Puche Julia, León Rafael, Pérez-Nadales Elena, Muñoz de la Rosa Monserrat, Natera Alejandra Mendez, Castón Juan José, Cano Ángela, Pineda-Capitán Juan Jesús, López Cristina, De la Fuente-Martos Carmen, Torre-Cisneros Julián, Martínez-Martínez Luis
Intensive Care Unit, Reina Sofia University Hospital, Cordoba, Spain; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Cordoba, Spain; CIBER de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain.
Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Cordoba, Spain; Microbiology Unit, Reina Sofia University Hospital, Córdoba, Spain.
J Glob Antimicrob Resist. 2025 Mar;41:138-143. doi: 10.1016/j.jgar.2024.12.013. Epub 2024 Dec 28.
To evaluate the efficacy of high-dose intravenous fosfomycin for the treatment of urinary tract infections (UTI) caused by KPC carbapenemase-producing Klebsiella pneumoniae (KPC-Kp). A secondary objective was to evaluate the impact of the results of fosfomycin susceptibility testing on prognosis.
This is an observational and retrospective study. Patients hospitalized with UTI caused by KPC-Kp receiving treatment with high-dose intravenous fosfomycin were evaluated from December 2012 to June 2018. The primary outcome variable was clinical cure at d 21.
Forty-seven patients were included. The results of commercial microdilution panels showed that KPC-Kp isolates from 14 (29.8%) and 33 (70.2%) patients were non-susceptible and susceptible to fosfomycin, respectively. In 28 available isolates, susceptibility was also determined by the reference agar dilution method. In the global cohort, clinical cure was achieved at d 21 for 33 (70.2%) out of the 47 patients, with no statistical differences found between fosfomycin non-susceptible isolates and fosfomycin susceptible isolates as determined by commercial microdilution (78.6 vs. 66.7%; P = 0.50) or by the reference agar dilution (83.3 vs. 72.7%; P = 1). In the logistic regression analysis, the Pitt index was the only variable related to clinical cure at 21 d. No statistically significant differences were found for the variables associated with fosfomycin susceptibility testing or fosfomycin minimum inhibitory concentration.
High-dose intravenous fosfomycin can be considered for treatment of hospitalized patients with KPC-Kp UTI in some scenarios. in vitro fosfomycin susceptibility testing for multiresistant KPC-Kp may be of limited clinical value.
评估大剂量静脉注射磷霉素治疗产KPC碳青霉烯酶肺炎克雷伯菌(KPC-Kp)所致尿路感染(UTI)的疗效。次要目的是评估磷霉素药敏试验结果对预后的影响。
这是一项观察性回顾性研究。对2012年12月至2018年6月期间因KPC-Kp所致UTI住院并接受大剂量静脉注射磷霉素治疗的患者进行评估。主要结局变量为第21天的临床治愈情况。
纳入47例患者。商业微量稀释法检测结果显示,分别有14例(29.8%)和33例(70.2%)患者的KPC-Kp分离株对磷霉素不敏感和敏感。在28株可获得的分离株中,药敏性也通过参考琼脂稀释法确定。在整个队列中,47例患者中有33例(70.2%)在第21天实现临床治愈,通过商业微量稀释法(78.6%对66.7%;P = 0.50)或参考琼脂稀释法(83.3%对72.7%;P = 1)确定,磷霉素不敏感分离株和磷霉素敏感分离株之间未发现统计学差异。在逻辑回归分析中,Pitt指数是与第21天临床治愈相关的唯一变量。与磷霉素药敏试验或磷霉素最低抑菌浓度相关的变量未发现统计学显著差异。
在某些情况下,大剂量静脉注射磷霉素可考虑用于治疗KPC-Kp所致UTI的住院患者。对多重耐药KPC-Kp进行体外磷霉素药敏试验的临床价值可能有限。