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脓肿分枝杆菌复合体的体外药敏试验及标准化治疗方案的可行性。

In vitro susceptibility of Mycobacterium abscessus complex and feasibility of standardizing treatment regimens.

机构信息

Department of Laboratory Medicine, National University Hospital, Singapore, Republic of Singapore.

National Public Health Laboratory, National Centre for Infectious Diseases, Singapore, Republic of Singapore.

出版信息

J Antimicrob Chemother. 2021 Mar 12;76(4):973-978. doi: 10.1093/jac/dkaa520.

DOI:10.1093/jac/dkaa520
PMID:33338230
Abstract

OBJECTIVES

To determine the in vitro susceptibility of members of the Mycobacterium abscessus complex to routinely tested antibiotics and to an extended antibiotic panel.

METHODS

Non-duplicate isolates for which susceptibility testing results were available were included in this study. Retrospective laboratory records were reviewed, including tigecycline susceptibility results, and testing was performed with additional drugs, including vancomycin, dalbavancin, telavancin, oritavancin, rifabutin, delafloxacin, eravacycline, clofazimine and bedaquiline using broth microdilution (Sensititre, Thermo Fisher).

RESULTS

A total of 218 M. abscessus complex isolates were included for retrospective review, of which 151 were respiratory isolates. Of these 218 isolates, 211 were available for additional testing with the extended antibiotic panel. Of these, 146 were respiratory isolates. One isolate had a vancomycin MIC of 2 mg/L and MICs of all other isolates were >8 mg/L. All isolates had MICs of >8 mg/L for oritavancin, dalbavancin and telavancin. One isolate had a delafloxacin MIC of 4 mg/L and MICs of all other isolates were >8 mg/L. The MIC50/MIC90s of rifabutin, tigecycline, eravacycline, clofazimine and bedaquiline were 16/32, 0.5/1, 0.12/0.25, 0.12/0.25 and 0.06/0.12 mg/L, respectively.

CONCLUSIONS

In vitro activity was demonstrated for clofazimine, bedaquiline and eravacycline, indicating potential for inclusion as standardized therapy for M. abscessus complex infections.

摘要

目的

确定脓肿分枝杆菌复合体成员对常规测试抗生素和扩展抗生素谱的体外敏感性。

方法

本研究纳入了药敏试验结果可用的非重复分离株。回顾了回顾性实验室记录,包括替加环素药敏试验结果,并使用肉汤微量稀释法(Sensititre,Thermo Fisher)对万古霉素、达巴万星、替拉万星、奥利万星、利福布汀、德拉沙星、依拉环素、氯法齐明和贝达喹啉等其他药物进行了检测。

结果

共回顾性分析了 218 株脓肿分枝杆菌复合体分离株,其中 151 株为呼吸道分离株。在这 218 株分离株中,有 211 株可用于进一步用扩展抗生素谱进行检测。其中,146 株为呼吸道分离株。1 株万古霉素 MIC 为 2mg/L,其余所有分离株 MIC 均>8mg/L。所有分离株的 MIC 均>8mg/L 用于奥利万星、达巴万星和替拉万星。1 株德拉沙星 MIC 为 4mg/L,其余所有分离株 MIC 均>8mg/L。利福布汀、替加环素、依拉环素、氯法齐明和贝达喹啉的 MIC50/MIC90 分别为 16/32、0.5/1、0.12/0.25、0.12/0.25 和 0.06/0.12mg/L。

结论

体外活性证实了氯法齐明、贝达喹啉和依拉环素的活性,表明它们可能被纳入脓肿分枝杆菌复合体感染的标准化治疗方案中。

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