In vitro investigation of synergy among fosfomycin and parenteral antimicrobials against carbapenemase-producing Enterobacteriaceae

被引:13
作者
Avery, Lindsay M. [1 ]
Sutherland, Christina A. [1 ]
Nicolau, David P. [1 ,2 ]
机构
[1] Hartford Hosp, Ctr Antiinfect Res & Dev, Hartford, CT 06115 USA
[2] Hartford Hosp, Div Infect Dis, Hartford, CT 06115 USA
关键词
Enterobacteriaceae; Carbapenemase; Synergy; Fosfomycin; RESISTANT KLEBSIELLA-PNEUMONIAE; TIME-KILL; ACINETOBACTER-BAUMANNII; ANTIBIOTIC SYNERGY; SUSCEPTIBILITY; CHECKERBOARD; INFECTIONS; STRATEGIES; ETEST; BACK;
D O I
10.1016/j.diagmicrobio.2019.05.014
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Intravenous fosfomycin is undergoing clinical development in the United States for treatment of complicated urinary tract infections (cUTIs) and may be prescribed as a component of dual antibiotic regimens against carbapenemase-producing Enterobacteriaceae (CPE). Fosfomycin, aztreonam, cefepime, ceftazidime, ceftazidime/avibactam, ceftolozane/tazobactam, meropenem, piperacillin/tazobactam, and tobramycin minimum inhibitory concentrations (MlC5) were determined by gradient diffusion strip (GDS) against CPE isolates (N = 49). The GDS cross method was used to assess antibiotic interactions between fosfomycin and the aforementioned parenteral antibiotics. The resultant fractional inhibitory concentration index was used to classify interactions. Fosfomycin-containing combinations were evaluated only if nonsusceptible to the second agent. The fosfomycin MIC50 was >= 1024 mg/L by GDS. Synergy or additivity was detected in 80 (22%) fosfomycin-containing combinations. Antagonism was not observed. Ceftolozane/tazobactam most frequently displayed synergy [8 (16.3%) isolates]. When CPE are isolated, clinical laboratories should consider performing GDS synergy tests to identify favorable antibiotic interactions. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:216 / 220
页数:5
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