Ceftolozane/tazobactam activity tested against Gram-negative bacterial isolates from hospitalised patients with pneumonia in US and European medical centres (2012)

被引:134
作者
Farrell, David J. [1 ]
Sader, Helio S. [1 ]
Flamm, Robert K. [1 ]
Jones, Ronald N. [1 ]
机构
[1] JMI Labs, North Liberty, IA 52317 USA
关键词
Ceftolozane/tazobactam; Pneumonia; Nosocomial; Surveillance; CEPHALOSPORIN CXA-101 FR264205; PENICILLIN-BINDING PROTEINS; PSEUDOMONAS-AERUGINOSA; BETA-LACTAMASE; IN-VITRO; TAZOBACTAM; PHARMACOKINETICS; INFECTION; DRUGS; PUMPS;
D O I
10.1016/j.ijantimicag.2014.01.032
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
During 2012, a total of 2968 isolates were consecutively collected from 59 medical centres in the USA and 15 European countries from hospitalised patients with pneumonia. Ceftolozane/tazobactam (tazobactam at a fixed concentration of 4 mg/L) and comparator agents were tested by reference methods, and MIC endpoints were interpreted by CLSI (2013) and EUCAST (2013) breakpoint criteria. Pseudomonas aeruginosa was the most common isolated pathogen (1019 strains; 34.3%), and ceftolozane/tazobactam was the most active p-lactam tested against P. aeruginosa (MIC50190, 0.5/4 mg/L; 94.1% inhibited at <8 mg/L). P. aeruginosa exhibited moderate susceptibility to meropenem (MIC50/90, 0.51>8 mg/L; 73.7% susceptible), ceftazidime (MIC50/90, 2/>32 mg/L; 73.6% susceptible), cefepime (MIC50/90, 41>16 mg/L; 76.5% susceptible), piperacillin/tazobactam (MIC50/90, 81>64 mg/L; 69.5% susceptible), levofloxacin [MIC50/90, 0.51>4 mg/L; 69.9161.0% susceptible ( CLSI/EUCAST criteria)] and gentamicin (MIC50/90, 21>8 mg/L; 80.7% susceptible). Ceftolozane/tazobactam exhibited activity against many ceftazidime-non-susceptible, meropenem-nonsusceptible and piperacillin/tazobactam-non-susceptible, multidrug-resistant (MDR) and extensively drug-resistant (XDR) P. aeruginosa isolates. Ceftolozane/tazobactam was active (MIC50/90, 0.2514 mg/L; 94.6% inhibited at <8 mg/L) against 1530 Enterobacteriaceae, including activity against many MDR and XDR strains. MDR and XDR prevalence varied widely between countries both for P. aeruginosa (24.1% MDR and 17.1% XDR overall) and Enterobacteriaceae (15.4% MDR and 2.7% XDR overall). All p-lactams had limited activity againstAcinetobacter spp. and Stenotrophomonas maltophilia. Ceftolozane/tazobactam demonstrated greater in vitro activity than currently available cephalosporins, carbapenems and piperacillin/tazobactam when tested against P. aeruginosa. In addition, ceftolozane/tazobactam demonstrated greater activity than contemporary cephalosporins and piperacillin/tazobactam when tested against most Enterobacteriaceae. (C) 2014 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
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页码:533 / 539
页数:7
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