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碳青霉烯类耐药肠杆菌科细菌和铜绿假单胞菌中头孢他啶-阿维巴坦和头孢唑南-他唑巴坦药敏检测方法的验证。

Verification of Ceftazidime-Avibactam and Ceftolozane-Tazobactam Susceptibility Testing Methods against Carbapenem-Resistant Enterobacteriaceae and Pseudomonas aeruginosa.

机构信息

Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

XDR Pathogen Laboratory, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

出版信息

J Clin Microbiol. 2018 Jan 24;56(2). doi: 10.1128/JCM.01093-17. Print 2018 Feb.

Abstract

Ceftazidime-avibactam and ceftolozane-tazobactam are newly approved agents for the treatment of infections caused by multidrug-resistant Gram-negative bacteria. Resistance to both agents has been described clinically. Susceptibility testing on automated systems is unavailable for either agent. Our objective was to compare the disk diffusion and Etest methods to standard broth microdilution (BMD) methods for testing ceftazidime-avibactam and ceftolozane-tazobactam against a diverse collection of carbapenem-resistant (CRE) and carbapenem-resistant (CRP) isolates, respectively. Among 74 ceftazidime-avibactam-susceptible and -resistant CRE isolates, BMD categorical agreement was higher with Etest (96%) than with disk diffusion (72%; = 0.0003). Twenty-eight percent of ceftazidime-avibactam-susceptible CRE isolates were classified as resistant by disk diffusion. Results were comparable to those obtained with resistance defined genotypically. Among 72 ceftolozane-tazobactam-susceptible and -resistant CRP isolates, the levels of BMD categorical agreement with disk diffusion and Etest were 94% and 96%, respectively; the only errors identified were minor. Our findings demonstrate that Etest measurements of ceftazidime-avibactam and ceftolozane-tazobactam susceptibility correlate closely with standard BMD methods, suggesting a useful role clinically. On the other hand, disk diffusion measurements overcalled CRE resistance to ceftazidime-avibactam. A better understanding of ceftazidime-avibactam interpretive breakpoints is needed before disk diffusion is used routinely in the clinic. Until clinicians and microbiologists understand Etest and disk diffusion performance at their centers, test results should be interpreted cautiously.

摘要

头孢他啶-阿维巴坦和头孢洛扎米-他唑巴坦是新批准的用于治疗多重耐药革兰氏阴性菌感染的药物。这两种药物都已在临床上描述过耐药性。两种药物的自动化系统敏感性测试都不可用。我们的目的是比较纸片扩散法和 Etest 法与标准肉汤微量稀释(BMD)法,分别检测不同的碳青霉烯类耐药(CRE)和碳青霉烯类耐药(CRP)分离株对头孢他啶-阿维巴坦和头孢洛扎米-他唑巴坦的敏感性。在 74 株头孢他啶-阿维巴坦敏感和耐药的 CRE 分离株中,Etest(96%)的 BMD 分类一致性高于纸片扩散法(72%;=0.0003)。28%的头孢他啶-阿维巴坦敏感的 CRE 分离株被纸片扩散法分类为耐药。结果与通过基因分型定义的耐药性相符。在 72 株头孢洛扎米-他唑巴坦敏感和耐药的 CRP 分离株中,BMD 与纸片扩散法和 Etest 的分类一致性水平分别为 94%和 96%;仅发现了微小误差。我们的研究结果表明,Etest 测量头孢他啶-阿维巴坦和头孢洛扎米-他唑巴坦的敏感性与标准 BMD 方法密切相关,这在临床上具有重要作用。另一方面,纸片扩散法高估了 CRE 对头孢他啶-阿维巴坦的耐药性。在临床上常规使用纸片扩散法之前,需要更好地了解头孢他啶-阿维巴坦的解释性断点。在临床医生和微生物学家了解其中心的 Etest 和纸片扩散法的性能之前,应谨慎解释测试结果。

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