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头孢唑林对有指征的肠杆菌科细菌尿液头孢菌素活性的预测作用。

Cefazolin as a predictor of urinary cephalosporin activity in indicated Enterobacterales.

机构信息

Department of Pathology, Virginia Commonwealth University Health System, Richmond, Virginia, USA.

Scientific and Medical Affairs Consulting, Newton, Pennsylvania, USA.

出版信息

J Clin Microbiol. 2024 Apr 10;62(4):e0078821. doi: 10.1128/jcm.00788-21. Epub 2024 Mar 8.

Abstract

Traditionally, cephalothin susceptibility results were used to predict the susceptibility of additional cephalosporins; however, in 2013-2014, the Clinical and Laboratory Standards Institute (CLSI) revisited this practice and determined that cefazolin is a more accurate proxy than cephalothin for uncomplicated urinary tract infections (uUTIs). Therefore, a cefazolin surrogacy breakpoint was established to predict the susceptibility of seven oral cephalosporins for , , and in the context of uUTIs. Clinical microbiology laboratories face several operational challenges when implementing the cefazolin surrogacy breakpoint, which may lead to confusion for the best path forward. Here, we review the historical context and data behind the surrogacy breakpoints, review PK/PD profiles for oral cephalosporins, discuss challenges in deploying the breakpoint, and highlight the limited clinical outcome data in this space.

摘要

传统上,头孢菌素药敏结果用于预测其他头孢菌素的药敏性;然而,在 2013-2014 年,临床和实验室标准协会(CLSI)重新审视了这一做法,并确定头孢唑林对于简单性尿路感染(uUTIs)比头孢噻吩更能准确替代。因此,建立了头孢唑林替代物折点,以预测七种口服头孢菌素在 uUTIs 情况下对 、 、 和 的药敏性。临床微生物学实验室在实施头孢唑林替代物折点时面临着几个操作挑战,这可能会导致在最佳前进道路上产生混淆。在这里,我们回顾了替代物折点背后的历史背景和数据,回顾了口服头孢菌素的 PK/PD 特征,讨论了部署折点的挑战,并强调了这一领域有限的临床结果数据。

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