Pharmacodynamics of Ceftolozane Combined with Tazobactam against Enterobacteriaceae in a Neutropenic Mouse Thigh Model

被引:33
作者
Melchers, M. J. [1 ]
Mavridou, E. [1 ,4 ]
van Mil, A. C. [1 ,2 ]
Lagarde, C. [1 ]
Mouton, J. W. [1 ,3 ]
机构
[1] Radboud Univ Nijmegen Med Ctr, Dept Med Microbiol, Nijmegen, Netherlands
[2] Canisius Wilhelmina Hosp, Nijmegen, Netherlands
[3] Erasmus MC, Dept Med Microbiol & Infect Dis, Rotterdam, Netherlands
[4] Div Infect Dis, Weill Cornell Med, Transplantation Oncol Infect Dis Program, New York, NY USA
关键词
LACTAMASE-PRODUCING ENTEROBACTERIACEAE; SPECTRUM BETA-LACTAMASES; IN-VIVO; PSEUDOMONAS-AERUGINOSA; CXA-101; FR264205; COMBINATION; MICE; INHIBITOR; PHARMACOKINETICS; CEPHALOSPORIN;
D O I
10.1128/AAC.01580-16
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Ceftolozane is a new broad-spectrum cephalosporin and is combined with tazobactam to broaden the activity of ceftolozane against strains producing extended-spectrum beta-lactamases (ESBLs). We determined the pharmacodynamics (PD) of the combination in the neutropenic mouse thigh model to determine the optimal exposure of tazobactam. Treatment of CD-1 neutropenic mice was started 2 h after infection with ceftolozane every 2 h (q2h) alone or in combination with tazobactam at different dosing frequencies for 24 h, and the number of CFU in the thighs was determined before and after treatment. The maximum effect model was fit to the dose-response and the pharmacokinetic/PD index (PDI)-response to determine the PDI values for ceftolozane alone and ceftolozane in combination with tazobactam resulting in a static effect and a 1-log kill. The effect of tazobactam was dependent on the percentage of time that the free drug concentration remained above the concentration threshold (percent fT(>CT)), whereby dosing q2h was more efficacious than dosing every 8 h (q8h), reducing the tazobactam daily dose by a factor 6.9 to 59.0 (n = 3 strains) to obtain a static effect. Using R-2 as an indicator of the best fit of the percent fT(>CT)-response relationships, the concentration threshold best correlating with the response varied from 0.5 to 2 mg/liter, depending on the strain. A similar result was obtained when the q2h and q8h regimens were analyzed. For all isolates tested, the mean fT(>CT) for 0.5 mg/liter tazobactam was 28.2% (range, 17.5 to 45.8%) and 44.4% (range, 26.6 to 54.7%) for a static effect and a 1-log kill, respectively, at ceftolozane exposures that produced a ceftolozane concentration of 4 mg/liter (a concentration greater than the MIC) for 33.9 to 63.3% of a 24-h period under steady-state pharmacokinetic conditions. The main PDI that correlated with the effect of tazobactam was the fT(>CT) achieved with a C-T of 0.5 mg/liter tazobactam.
引用
收藏
页码:7272 / 7279
页数:8
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