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头孢地尔罗:一种针对多重耐药感染的有效抗菌药物,但对常规抗菌药物敏感性测试构成挑战。

Cefiderocol - An effective antimicrobial for MDR infections but a challenge for routine antimicrobial susceptibility testing.

机构信息

Department of Microbiology and Laboratory Medical Immunology, Medical University of Lodz, Lodz, Poland; Medical Microbiology Laboratory, Central Teaching Hospital of Medical University of Lodz, Lodz, Poland.

Department of Microbiology and Laboratory Medical Immunology, Medical University of Lodz, Lodz, Poland; Medical Microbiology Laboratory, Central Teaching Hospital of Medical University of Lodz, Lodz, Poland.

出版信息

Adv Med Sci. 2024 Sep;69(2):256-263. doi: 10.1016/j.advms.2024.05.001. Epub 2024 May 21.

Abstract

PURPOSE

Cefiderocol is a novel cephalosporin-siderophore conjugate antibiotic that holds promise to thwart infections caused by multi-drug-resistant gram-negative bacilli. Its antibacterial activity against normally susceptible species is not affected by most β-lactamases, including metallo-β-lactamases. Due to the siderophore-mediated entry into the cell, the activity of cefiderocol is less affected by porin loss or active efflux resistance than many other β-lactam antibiotics. The aim of this study was to assess in vitro susceptibility to the cefiderocol of carbapenemase-producing gram-negative bacilli from clinical samples of hospitalized patients.

MATERIALS AND METHODS

We analyzed 102 clinical strains of carbapenemase-producing Enterobacterales and non-fermentives from hospital centers in Łódź, Poland. Antimicrobial susceptibility to cefiderocol was tested by the minimum inhibitory concentration test strips and disc diffusion methods.

RESULTS

The obtained results turned out to be ambiguous, and the area of technical uncertainty made their interpretation very difficult.

CONCLUSIONS

The cost of therapy with this antibiotic, and difficulties in interpreting the drug susceptibility are the limitations to the use of cefiderocol. Intensive work should be carried out to finally standardize an easily accessible and reliable method for the determination of susceptibility to cefiderocol.

摘要

目的

头孢他啶-多粘菌素 E 是一种新型头孢菌素-铁载体化合物抗生素,有望阻止多药耐药革兰氏阴性杆菌引起的感染。其对通常敏感的物种的抗菌活性不受大多数β-内酰胺酶(包括金属β-内酰胺酶)的影响。由于铁载体介导的进入细胞,头孢他啶的活性受孔蛋白缺失或主动外排耐药的影响小于许多其他β-内酰胺类抗生素。本研究旨在评估头孢他啶对来自波兰罗兹医院中心住院患者临床样本中产碳青霉烯酶的革兰氏阴性杆菌的体外药敏情况。

材料和方法

我们分析了来自波兰罗兹医院中心的 102 株产碳青霉烯酶肠杆菌科和非发酵菌临床株。采用最低抑菌浓度测试条和纸片扩散法检测头孢他啶的药敏性。

结果

结果模棱两可,技术不确定区域使得解释非常困难。

结论

该抗生素治疗费用高,药敏解读困难,限制了头孢他啶的使用。应开展深入研究,最终为头孢他啶药敏测定制定一种易于获得且可靠的标准化方法。

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