Evaluation of gradient strip diffusion for susceptibility testing of aztreonam-avibactam in metallo-β-lactamase-producing Enterobacterales

被引:1
作者
Lemon, Jamie K. [1 ,2 ]
Jankowsi-Romano, Cheryl [1 ]
Duong, Scott [1 ,2 ]
Juretschko, Stefan [1 ,2 ]
Streva, Vincent A. [1 ,2 ]
机构
[1] Northwell Hlth Clin Labs, New York, NY 10075 USA
[2] Donald & Barbara Zucker Sch Med Hofstra Northwell, Manhasset, NY 11549 USA
关键词
metallo-beta-lactamase; aztreonam-avibactam; antimicrobial susceptibility testing; NDM; gradient strip diffusion;
D O I
10.1128/jcm.00649-24
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The emergence of metallo-beta-lactamase (MBL)-producing Enterobacterales presents unique clinical treatment challenges. Recently developed beta-lactam/ beta-lactamase inhibitor combination agents, while effective against other carbapenemase-producing organisms, are notably ineffective against MBL producers. While MBLs do not hydrolyze monobactams (aztreonam), many MBL-producing organisms are resistant to aztreonam through alternate mechanisms, leaving cefiderocol as the sole monotherapy treatment option recommended for MBL producers. Recent guidelines for the treatment of MBL-harboring organisms have added combination therapy with aztreonam and ceftazidime-avibactam, using ceftazidime-avibactam as a source of the beta-lactamase inhibitor avibactam. Current laboratory testing options for the combination of aztreonam-avibactam are limited to broth microdilution (BMD) and broth disk elution (BDE) methods, which are not practical in most clinical laboratories. In this study, we evaluated the performance of aztreonam/avibactam gradient strips on 103 MBL-producing Enterobacterales patient isolates as well as an additional 31 isolates from the CDC AR Bank. All MBL Enterobacterales patient isolates included in this study harbored a New Delhi metallo-beta-lactamase (blaNDM) gene. Essential agreement of gradient strip minimal inhibitory concentrations (MICs) for patient isolates compared to BMD was 93.2%. While there are no established breakpoints for aztreonam-avibactam, category agreement (CA) for patient isolates was 97.1% when using the CLSI aztreonam breakpoints. There were no major or very major errors observed. There were three minor errors. Precision for aztreonam-avibactam gradient strip diffusion was 100%. These data demonstrate that the use of gradient strip diffusion for aztreonam-avibactam MIC determination in MBL-producing Enterobacterales is a viable option for clinical laboratories.
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页数:10
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