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头孢洛扎/他唑巴坦对多种克隆谱系产超广谱β-内酰胺酶和碳青霉烯酶革兰阴性菌的药敏试验

Ceftolozane/Tazobactam Susceptibility Testing in Extended-Spectrum Betalactamase- and Carbapenemase-Producing Gram-Negative Bacteria of Various Clonal Lineages.

作者信息

Pazzini Carlo, Ahmad-Nejad Parviz, Ghebremedhin Beniam

机构信息

Faculty of Health, Center for Clinical and Translational Research, Institute of Medical Laboratory Diagnostics, HELIOS University Clinic Wuppertal, Witten/Herdecke University, Witten, Germany.

出版信息

Eur J Microbiol Immunol (Bp). 2019 Feb 8;9(1):1-4. doi: 10.1556/1886.2019.00001. eCollection 2019 Mar 18.

Abstract

Nowadays, multidrug-resistant bacteria are considered as an increasing serious threat to public health worldwide. Global and local surveillance data are helpful in the application of the most efficient antimicrobial agent in bacterial infections. In the current study, we aimed to analyze the activity of the previously cleared agent ceftolozane/ tazobactam (C/T) in African and European multidrug-resistant Gram-negative bacteria. Susceptibility testing was performed on 147 extended-spectrum β-lactamase (107 and 40 ) and 103 carbapenemase-producing Gram-negative bacteria using Etest according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) clinical breakpoints. Among the extended-spectrum β-lactamase producing isolates, 91 isolates (85%) and 23 (57.5%) were susceptible towards C/T whereas out of the 103 carbapenemase-producing isolates 102 (99.0%) were C/T-resistant. C/T should be included in susceptibility testing to fairly administer this antimicrobial agent in infections caused by multidrug-resistant bacteria. It may be considered as a therapy option for infections caused by extended-spectrum β-lactamase-producing bacteria once susceptibility to this antimicrobial combination has been confirmed.

摘要

如今,耐多药细菌被认为是对全球公共卫生日益严重的威胁。全球和本地监测数据有助于在细菌感染中应用最有效的抗菌药物。在本研究中,我们旨在分析先前已获批的药物头孢洛扎/他唑巴坦(C/T)对非洲和欧洲耐多药革兰氏阴性菌的活性。根据欧洲抗菌药物敏感性试验委员会(EUCAST)临床断点,使用Etest对147株产超广谱β-内酰胺酶(107株和40株)和103株产碳青霉烯酶革兰氏阴性菌进行药敏试验。在产超广谱β-内酰胺酶的分离株中,91株(85%)和23株(57.5%)对C/T敏感,而在103株产碳青霉烯酶的分离株中,102株(99.0%)对C/T耐药。在耐多药细菌引起的感染中,应将C/T纳入药敏试验,以便合理使用这种抗菌药物。一旦证实对这种抗菌药物组合敏感,C/T可被视为产超广谱β-内酰胺酶细菌引起的感染的治疗选择。

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