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如何根据修订后的临床折点 v.10.0 欧洲抗菌药物敏感性试验委员会 (EUCAST) 来解释抗真菌化合物的 MIC 值。

How to interpret MICs of antifungal compounds according to the revised clinical breakpoints v. 10.0 European committee on antimicrobial susceptibility testing (EUCAST).

机构信息

Unit of Mycology, Department of Microbiological Surveillance and Research, Statens Serum Institut, Copenhagen, Denmark; Department of Clinical Microbiology, University Hospital Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Division of Clinical Microbiology, Helsinki University Hospital, HUSLAB, Finland.

出版信息

Clin Microbiol Infect. 2020 Nov;26(11):1464-1472. doi: 10.1016/j.cmi.2020.06.007. Epub 2020 Jun 17.

Abstract

BACKGROUND

EUCAST has revised the definition of the susceptibility category I from 'Intermediate' to 'Susceptible, Increased exposure'. This implies that I can be used where the drug concentration at the site of infection is high, either because of dose escalation or through other means to ensure efficacy. Consequently, I is no longer used as a buffer zone to prevent technical factors from causing misclassifications and discrepancies in interpretations. Instead, an Area of Technical Uncertainty (ATU) has been introduced for MICs that cannot be categorized without additional information as a warning to the laboratory that decision on how to act has to be made. To implement these changes, the EUCAST-AFST (Subcommittee on Antifungal Susceptibility Testing) reviewed all, and revised some, clinical antifungal breakpoints.

OBJECTIVES

The aim was to present an overview of the current antifungal breakpoints and supporting evidence behind the changes.

SOURCES

This document is based on the ten recently updated EUCAST rationale documents, clinical breakpoint and breakpoint ECOFF documents.

CONTENT

The following breakpoints (in mg/L) have been revised or established for Candida species: micafungin against C. albicans (ATU = 0.03); amphotericin B (S ≤/> R = 1/1), fluconazole (S ≤/> R = 2/4), itraconazole (S ≤/> R = 0.06/0.06), posaconazole (S ≤/> R = 0.06/0.06) and voriconazole (S ≤/> R = 0.06/0.25) against C. dubliniensis; fluconazole against C. glabrata (S ≤/> R = 0.001/16); and anidulafungin (S ≤/> R = 4/4) and micafungin (S ≤/> R = 2/2) against C. parapsilosis. For Aspergillus, new or revised breakpoints include itraconazole (ATU = 2) and isavuconazole against A. flavus (S ≤/> R = 1/2, ATU = 2); amphotericin B (S ≤/> R = 1/1), isavuconazole (S ≤ /> R = 1/2, ATU = 2), itraconazole (S ≤/> R = 1/1, ATU = 2), posaconazole (ATU = 0.25) and voriconazole (S ≤/> R = 1/1, ATU = 2) against A. fumigatus; itraconazole (S ≤/> R = 1/1, ATU = 2) and voriconazole (S ≤/> R = 1/1, ATU = 2) against A. nidulans; amphotericin B against A. niger (S ≤/> R = 1/1); and itraconazole (S ≤/> R = 1/1, ATU = 2) and posaconazole (ATU = 0.25) against A. terreus.

IMPLICATIONS

EUCAST-AFST has released ten new documents summarizing existing and new breakpoints and MIC ranges for control strains. A failure to adopt the breakpoint changes may lead to misclassifications and suboptimal or inappropriate therapy of patients with fungal infections.

摘要

背景

EUCAST 修订了“中介”药敏分类为“敏感,增加暴露”。这意味着当感染部位的药物浓度较高时,可以使用 I 类(中介),无论是因为剂量升级还是通过其他手段确保疗效。因此,I 不再作为防止技术因素导致分类错误和解释差异的缓冲区。相反,引入了一个技术不确定区(ATU),用于无法归类的 MIC,这是一个警告,提示实验室必须做出如何行动的决定。为了实施这些变化,EUCAST-AFST(抗真菌药敏检测小组委员会)审查了所有的临床抗真菌折点,并修订了其中一些。

目的

介绍当前抗真菌折点的概述以及背后的变化依据。

来源

本文件基于最近更新的十个 EUCAST 原理文件、临床折点和折点 ECOFF 文件。

内容

对白色念珠菌等念珠菌属和烟曲霉等曲霉菌属的药物折点进行了修订或建立:米卡芬净(ATU = 0.03);两性霉素 B(S > R = 1/1)、氟康唑(S > R = 2/4)、伊曲康唑(S > R = 0.06/0.06)、泊沙康唑(S > R = 0.06/0.06)和伏立康唑(S > R = 0.06/0.25);氟康唑(S > R = 0.001/16);阿尼芬净(S > R = 4/4)和米卡芬净(S > R = 2/2)。对于烟曲霉,新的或修订的折点包括伊曲康唑(ATU = 2)和伊曲康唑(ATU = 2);两性霉素 B(S > R = 1/1)、伊曲康唑(S > R = 1/2,ATU = 2)、伏立康唑(S > R = 1/2,ATU = 2)、伊曲康唑(S > R = 1/1,ATU = 2)、泊沙康唑(ATU = 0.25)和伏立康唑(S > R = 1/1,ATU = 2);伊曲康唑(S > R = 1/1,ATU = 2)和伏立康唑(S > R = 1/1,ATU = 2);两性霉素 B(S > R = 1/1);伊曲康唑(S > R = 1/1,ATU = 2)和泊沙康唑(ATU = 0.25)。

影响

EUCAST-AFST 发布了十个新文件,总结了现有的和新的折点和 MIC 范围的对照菌株。如果不采用折点变化,可能会导致分类错误,以及真菌感染患者的治疗效果不佳或不适当。

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