Department of Pharmacy, Cleveland Clinic, Cleveland, Ohio, USA.
Antimicrob Agents Chemother. 2012 Nov;56(11):5744-8. doi: 10.1128/AAC.00402-12. Epub 2012 Aug 27.
Fosfomycin has shown promising in vitro activity against multidrug-resistant (MDR) urinary pathogens; however, clinical data are lacking. We conducted a retrospective chart review to describe the microbiological and clinical outcomes of urinary tract infections (UTIs) with MDR pathogens treated with fosfomycin tromethamine. Charts for 41 hospitalized patients with a urine culture for an MDR pathogen who received fosfomycin tromethamine from 2006 to 2010 were reviewed. Forty-one patients had 44 urinary pathogens, including 13 carbapenem-resistant Klebsiella pneumoniae (CR-Kp), 8 Pseudomonas aeruginosa, and 7 vancomycin-resistant Enterococcus faecium (VRE) isolates, 7 extended-spectrum beta-lactamase (ESBL) producers, and 9 others. In vitro fosfomycin susceptibility was 86% (median MIC, 16 μg/ml; range, 0.25 to 1,024 μg/ml). Patients received an average of 2.9 fosfomycin doses per treatment course. The overall microbiological cure was 59%; failure was due to either relapse (24%) or reinfection UTI (17%). Microbiological cure rates by pathogen were 46% for CR-Kp, 38% for P. aeruginosa, 71% for VRE, 57% for ESBL producers, and 100% for others. Microbiological cure (n = 24) was compared to microbiological failure (n = 17). There were significantly more solid organ transplant recipients in the microbiological failure group (59% versus 21%; P = 0.02). None of the patients in the microbiological cure group had a ureteral stent, compared to 24% of patients within the microbiological failure group (P = 0.02). Fosfomycin demonstrated in vitro activity against UTIs due to MDR pathogens. For CR-KP, there was a divergence between in vitro susceptibility (92%) and microbiological cure (46%). Multiple confounding factors may have contributed to microbiological failures, and further data regarding the use of fosfomycin for UTIs due to MDR pathogens are needed.
磷霉素对多种耐药(MDR)尿路感染病原体具有良好的体外活性,但临床数据有限。我们进行了一项回顾性图表审查,以描述 2006 年至 2010 年间用磷霉素氨丁三醇治疗 MDR 病原体引起的尿路感染(UTI)的微生物学和临床结果。对 41 例因 MDR 病原体尿液培养而接受磷霉素氨丁三醇治疗的住院患者的图表进行了回顾。41 例患者有 44 种尿病原体,包括 13 株耐碳青霉烯类肺炎克雷伯菌(CR-Kp)、8 株铜绿假单胞菌和 7 株万古霉素耐药粪肠球菌(VRE)分离株、7 株产超广谱β-内酰胺酶(ESBL)的病原体和 9 株其他病原体。体外磷霉素敏感性为 86%(中位数 MIC,16μg/ml;范围,0.25 至 1024μg/ml)。患者每疗程平均接受 2.9 次磷霉素治疗。总体微生物学治愈率为 59%;失败的原因是复发(24%)或再感染 UTI(17%)。根据病原体,CR-Kp 的微生物学治愈率为 46%,铜绿假单胞菌为 38%,VRE 为 71%,ESBL 产生菌为 57%,其他病原体为 100%。将微生物学治愈(n=24)与微生物学失败(n=17)进行比较。在微生物学失败组中,实体器官移植受者明显更多(59%比 21%;P=0.02)。微生物学治愈组中无一例患者有输尿管支架,而微生物学失败组中有 24%的患者有输尿管支架(P=0.02)。磷霉素对 MDR 病原体引起的 UTI 具有体外活性。对于 CR-KP,体外药敏性(92%)与微生物学治愈率(46%)之间存在差异。多种混杂因素可能导致微生物学失败,需要进一步研究磷霉素治疗 MDR 病原体引起的 UTI 的数据。