Evaluation of the In Vitro Activity of Ceftazidime-Avibactam and Ceftolozane-Tazobactam against Meropenem-Resistant Pseudomonas aeruginosa Isolates

被引:85
作者
Buehrle, Deanna J. [1 ]
Shields, Ryan K. [2 ,3 ]
Chen, Liang [4 ]
Hao, Binghua [3 ]
Press, Ellen G. [2 ]
Alkrouk, Ammar [2 ]
Potoski, Brian A. [1 ]
Kreiswirth, Barry N.
Clancy, Cornelius J. [2 ,3 ,5 ]
Nguyen, M. Hong [2 ,3 ]
机构
[1] Univ Pittsburgh, Dept Pharm & Therapeut, Pittsburgh, PA USA
[2] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
[3] Univ Pittsburgh, Med Ctr, XDR Pathogen Lab, Pittsburgh, PA USA
[4] Rutgers State Univ, Sch Med, Newark, NJ 07102 USA
[5] VA Pittsburgh Healthcare Syst, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
BETA-LACTAM RESISTANCE; BLOOD-STREAM INFECTIONS; GRAM-NEGATIVE ORGANISMS; US MEDICAL-CENTERS; CARBAPENEM RESISTANCE; KLEBSIELLA-PNEUMONIAE; MEDITERRANEAN COUNTRIES; CXA-101; FR264205; MECHANISMS; ENTEROBACTERIACEAE;
D O I
10.1128/AAC.02969-15
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:3227 / 3231
页数:5
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