期刊
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
卷 60, 期 5, 页码 3227-3231出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.02969-15
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资金
- HHS \ National Institutes of Health (NIH) [K08AI114883]
- NIH [R21AI222037]
We compared ceftazidime-avibactam, ceftolozane-tazobactam, ceftazidime, cefepime, and piperacillin-tazobactam MICs for 38 meropenem-resistant Pseudomonas aeruginosa isolates. No isolates harbored carbapenemases; 74% were oprD mutants. Ceftazidime-avibactam and ceftolozane-tazobactam were active against 92% of the isolates, including 80% that were resistant to all three beta-lactams. Forty-three percent of ceftazidime-avibactam-susceptible isolates and 6% of ceftolozane-tazobactam-susceptible isolates exhibited MICs at the respective breakpoints. Ceftolozane-tazobactam and ceftazidime-avibactam are therapeutic options for meropenem-resistant P. aeruginosa infections that should be used judiciously to preserve activity.
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