EUCAST breakpoints for antifungals.

Juan L Rodríguez-Tudela, Maiken C Arendrup, Manuel Cuenca-Estrella, J Peter Donnelly, Cornelia Lass-Flörl
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引用次数: 46

Abstract

Susceptibility testing of fungi and development of interpretative breakpoints has become increasingly important due to the growing incidence of invasive fungal infections, the number and classes of antifungals, and the emerging reports of acquired resistance. The subcommittee on antifungal susceptibility testing of the European Committee on Antibiotic Susceptibility Testing (EUCAST) has developed standards for susceptibility testing of fermentative yeasts and molds as well as proposing breakpoints for fluconazole and voriconazole against Candida. The aim of this work is to describe the EUCAST process of setting breakpoints for antifungals. Five aspects are evaluated during the process of developing breakpoints: 1) the most common dosage used in each European country, 2) the definition of the wild-type population for each target microorganism at the species level and the determination of epidemiological cutoffs, 3) the drug's pharmacokinetics and 4) pharmacodynamics, including Monte Carlo simulations, and 5) the correlation of MICs with clinical outcome of patients treated with the compound. When insufficient data are available (e.g., due to lack of information on the clinical outcome of infections caused by isolates with an elevated MIC), epidemiological cutoff values, rather than breakpoints, are recommended until the necessary information becomes available.

抗真菌药的EUCAST断点。
由于侵袭性真菌感染的发病率不断增加,抗真菌药物的数量和种类不断增加,以及获得性耐药性的新报道,真菌的药敏试验和解释性断点的发展变得越来越重要。欧洲抗生素药敏试验委员会(EUCAST)的抗真菌药敏试验小组委员会制定了发酵酵母和霉菌药敏试验标准,并提出了氟康唑和伏立康唑抗念珠菌的断点。这项工作的目的是描述EUCAST过程设置抗真菌药物的断点。在制定断点的过程中,评估了五个方面:1)每个欧洲国家最常用的剂量,2)每种目标微生物在物种水平上的野生型种群的定义和流行病学截止点的确定,3)药物的药代动力学和4)药效学,包括蒙特卡罗模拟,以及5)mic与接受该化合物治疗的患者临床结果的相关性。当可获得的数据不足时(例如,由于缺乏由MIC升高的分离株引起的感染的临床结果的信息),建议使用流行病学临界值,而不是断点,直到获得必要的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug news & perspectives
Drug news & perspectives 医学-药学
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