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Progress in Antifungal Susceptibility Testing of Candida spp. by Use of Clinical and Laboratory Standards Institute Broth Microdilution Methods, 2010 to 2012

机译:念珠菌抗真菌药敏试验的进展。通过使用临床和实验室标准协会的肉汤微稀释方法,2010年至2012年

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Antifungal susceptibility testing of Candida has been standardized and refined and now may play a useful role in managing Candida infections. Important new developments include validation of 24-h reading times for all antifungal agents and the establishment of species-specific epidemiological cutoff values (ECVs) for the systemically active antifungal agents and both common and uncommon species of Candida. The clinical breakpoints (CBPs) for fluconazole, voriconazole, and the echinocandins have been revised to provide species-specific interpretive criteria for the six most common species. The revised CBPs not only are predictive of clinical outcome but also provide a more sensitive means of identifying those strains with acquired or mutational resistance mechanisms. This brief review serves as an update on the new developments in the antifungal susceptibility testing of Candida spp. using Clinical and Laboratory Standards Institute (CLSI) broth microdilution (BMD) methods.
机译:念珠菌的抗真菌药敏试验已经标准化和完善,现在可能在控制念珠菌感染中发挥有用的作用。重要的新进展包括验证所有抗真菌药的24小时读取时间,以及确定具有系统活性的抗真菌药以及念珠菌的常见和罕见物种的物种特异性流行病学临界值(ECV)。氟康唑,伏立康唑和棘球and素的临床断点(CBP)已经过修订,为六个最常见的物种提供了特定于物种的解释标准。修订后的CBP不仅可以预测临床结果,而且还可以提供一种更灵敏的方法来鉴定具有获得性或突变性耐药机制的菌株。这篇简短的评论是对念珠菌抗真菌药敏试验的最新进展的更新。使用临床和实验室标准协会(CLSI)肉汤微稀释(BMD)方法。

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