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本文引用的文献

1
Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: Clinical Effectiveness and Evolution of Resistance.头孢洛扎他唑巴坦治疗多重耐药铜绿假单胞菌感染:临床疗效和耐药演变。
Clin Infect Dis. 2017 Jul 1;65(1):110-120. doi: 10.1093/cid/cix182.
2
Mutations in That Confer Ceftazidime-Avibactam Resistance Encode Novel KPC-3 Variants That Function as Extended-Spectrum β-Lactamases.赋予头孢他啶-阿维巴坦耐药性的突变编码新型KPC-3变体,其作为超广谱β-内酰胺酶发挥作用。
Antimicrob Agents Chemother. 2017 Apr 24;61(5). doi: 10.1128/AAC.02534-16. Print 2017 May.
3
Emergence of Ceftazidime-Avibactam Resistance Due to Plasmid-Borne Mutations during Treatment of Carbapenem-Resistant Klebsiella pneumoniae Infections.耐碳青霉烯类肺炎克雷伯菌感染治疗期间因质粒介导的突变导致头孢他啶-阿维巴坦耐药的出现
Antimicrob Agents Chemother. 2017 Feb 23;61(3). doi: 10.1128/AAC.02097-16. Print 2017 Mar.
4
Comparison of Etest to Broth Microdilution for Testing of Susceptibility of Pseudomonas aeruginosa to Ceftolozane-Tazobactam.Etest法与肉汤微量稀释法用于检测铜绿假单胞菌对头孢他啶-阿维巴坦敏感性的比较。
J Clin Microbiol. 2016 Dec 28;55(1):334-335. doi: 10.1128/JCM.01920-16. Print 2017 Jan.
5
Clinical Outcomes, Drug Toxicity, and Emergence of Ceftazidime-Avibactam Resistance Among Patients Treated for Carbapenem-Resistant Enterobacteriaceae Infections.耐碳青霉烯类肠杆菌科细菌感染患者的临床结局、药物毒性及头孢他啶-阿维巴坦耐药性的出现
Clin Infect Dis. 2016 Dec 15;63(12):1615-1618. doi: 10.1093/cid/ciw636. Epub 2016 Sep 13.
6
Effects of Klebsiella pneumoniae carbapenemase subtypes, extended-spectrum β-lactamases, and porin mutations on the in vitro activity of ceftazidime-avibactam against carbapenem-resistant K. pneumoniae.肺炎克雷伯菌碳青霉烯酶亚型、超广谱β-内酰胺酶及孔蛋白突变对头孢他啶-阿维巴坦体外抗碳青霉烯类耐药肺炎克雷伯菌活性的影响
Antimicrob Agents Chemother. 2015 Sep;59(9):5793-7. doi: 10.1128/AAC.00548-15. Epub 2015 Jul 13.
7
Doripenem, gentamicin, and colistin, alone and in combinations, against gentamicin-susceptible, KPC-producing Klebsiella pneumoniae strains with various ompK36 genotypes.多黏菌素、庆大霉素及二者联合用药对不同ompK36基因型的产KPC肺炎克雷伯菌(对庆大霉素敏感菌株)的抗菌活性研究
Antimicrob Agents Chemother. 2014 Jun;58(6):3521-5. doi: 10.1128/AAC.01949-13. Epub 2014 Feb 24.
8
Epidemiology and molecular characterization of bacteremia due to carbapenem-resistant Klebsiella pneumoniae in transplant recipients.移植受者碳青霉烯类耐药肺炎克雷伯菌菌血症的流行病学和分子特征。
Am J Transplant. 2013 Oct;13(10):2619-33. doi: 10.1111/ajt.12424. Epub 2013 Sep 6.
9
Multiplex real-time PCR for detection of an epidemic KPC-producing Klebsiella pneumoniae ST258 clone.多重实时 PCR 检测流行的产 KPC 肺炎克雷伯菌 ST258 克隆。
Antimicrob Agents Chemother. 2012 Jun;56(6):3444-7. doi: 10.1128/AAC.00316-12. Epub 2012 Mar 26.
10
Multiplex real-time PCR assay for detection and classification of Klebsiella pneumoniae carbapenemase gene (bla KPC) variants.多重实时 PCR 检测法用于检测和分类肺炎克雷伯菌碳青霉烯酶基因(bla KPC)变体。
J Clin Microbiol. 2011 Feb;49(2):579-85. doi: 10.1128/JCM.01588-10. Epub 2010 Dec 1.

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.

DOI:10.1128/JCM.01093-17
PMID:29167294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5786715/
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。