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体外研究亚胺培南-雷巴他定和替加环素对 102 株脓肿分枝杆菌分离株的药敏试验。

In vitro susceptibility testing of imipenem-relebactam and tedizolid against 102 Mycobacterium abscessus isolates.

机构信息

University of Queensland Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Australia; The Prince Charles Hospital, Brisbane, Australia.

Faculty of Medicine, The University of Queensland School of Medicine School of Medicine, Australia; Gallipoli Medical Research Institute, Brisbane, Australia.

出版信息

Int J Antimicrob Agents. 2023 Oct;62(4):106938. doi: 10.1016/j.ijantimicag.2023.106938. Epub 2023 Jul 28.

Abstract

OBJECTIVES

Mycobacterium abscessus is an emerging infection in people living with lung diseases, including cystic fibrosis (CF) and bronchiectasis, and it has limited treatment options and low cure rates. The off-label use of novel antibiotics developed for other bacterial pathogens offers potential new therapeutic options. We aimed to describe the in vitro activity of imipenem, imipenem-relebactam and tedizolid against comparator antibiotics in M. abscessus isolates from Australian patients with and without CF.

METHODS

We performed susceptibility testing for imipenem-relebactam, tedizolid and comparator antibiotics by Clinical and Laboratory Standards Institute (CLSI) criteria against 102 clinical M. abscessus isolates, including 46 from people with CF.

RESULTS

In this study, the minimum inhibitory concentration (MICs) of imipenem-relebactam was one-fold dilution less than of imipenem alone. The MIC and MIC of imipenem-relebactam were 8 and 16 mg/L, respectively, whereas for imipenem they were 16 and 32 mg/L. Tedizolid had an MIC and MIC of 2 and 4 mg/L, respectively. Forty non-CF isolates had linezolid susceptibility performed, with MIC and MIC values of 16 and 32 mg/L, respectively, measured.

CONCLUSIONS

This study shows lower MICs for imipenem-relebactam and tedizolid compared to other more commonly used antibiotics and supports their consideration in clinical trials for M. abscessus treatment.

摘要

目的

脓肿分枝杆菌是一种在患有肺部疾病(包括囊性纤维化(CF)和支气管扩张症)的人群中出现的新兴感染,其治疗选择有限,治愈率低。新型抗生素的非适应证使用为其他细菌病原体提供了潜在的新治疗选择。我们旨在描述美罗培南-雷巴他定和替加环素对澳大利亚 CF 患者和非 CF 患者的脓肿分枝杆菌分离株与对照抗生素相比的体外活性。

方法

我们根据临床和实验室标准协会(CLSI)标准,对 102 株临床脓肿分枝杆菌分离株(包括 46 株来自 CF 患者的分离株)进行了美罗培南-雷巴他定、替加环素和对照抗生素的药敏试验。

结果

在这项研究中,美罗培南-雷巴他定的最低抑菌浓度(MIC)比美罗培南单独使用低一个稀释度。美罗培南-雷巴他定的 MIC 和 MIC 分别为 8 和 16 mg/L,而美罗培南的 MIC 和 MIC 分别为 16 和 32 mg/L。替加环素的 MIC 和 MIC 分别为 2 和 4 mg/L。对 40 株非 CF 分离株进行了利奈唑胺药敏试验,其 MIC 和 MIC 值分别为 16 和 32 mg/L。

结论

与其他更常用的抗生素相比,美罗培南-雷巴他定和替加环素的 MIC 较低,支持将其用于脓肿分枝杆菌治疗的临床试验。

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