Department of Pathology, Division of Clinical Pathology, Penn State Hershey Medical Center and College of Medicine, Hershey, Pennsylvania, USA.
J Clin Microbiol. 2023 Apr 20;61(4):e0004223. doi: 10.1128/jcm.00042-23. Epub 2023 Mar 15.
In this issue of the , C. Manuel, R. Maynard, A. Abbott, K. Adams, et al. (J Clin Microbiol 61:e01617-22, 2023, https://doi.org/10.1128/JCM.01617-22) describe a multisite study evaluation of piperacillin-tazobactam (TZP) MIC testing on three U.S. Food and Drug Administration (FDA)-cleared antimicrobial susceptibility testing (AST) devices compared to the reference broth microdilution method for organisms belonging to . Although overall performance of each of the three devices was comparable when applying either FDA or Clinical and Laboratory Standards Institute (CLSI) TZP breakpoints, failure to update to the current CLSI breakpoints may result in falsely categorizing as many as 20% of the TZP-resistant isolates as susceptible. The impact of not updating clinical breakpoints and strategies for implementation of updated breakpoints are discussed.
在本期《临床微生物学杂志》中,C. Manuel、R. Maynard、A. Abbott、K. Adams 等人(J Clin Microbiol 61:e01617-22, 2023, https://doi.org/10.1128/JCM.01617-22)描述了一项多地点研究,评估了三种美国食品和药物管理局(FDA)批准的药敏检测设备(AST)上哌拉西林-他唑巴坦(TZP)MIC 检测与参考肉汤微量稀释法相比,对属于 菌属的生物体的检测性能。虽然在应用 FDA 或临床和实验室标准协会(CLSI)TZP 折点时,三种设备的总体性能相当,但如果不更新到当前的 CLSI 折点,可能会导致多达 20%的 TZP 耐药分离株被错误地归类为敏感。讨论了不更新临床折点的影响以及实施更新折点的策略。