A Pragmatic Approach to Susceptibility Classification of Yeasts without EUCAST Clinical Breakpoints.

Autor: Astvad KMT; Unit of Mycology, Statens Serum Institut, DK-2300 Copenhagen, Denmark., Arikan-Akdagli S; Department of Medical Microbiology, Hacettepe University Medical School, Ankara 06100, Turkey., Arendrup MC; Unit of Mycology, Statens Serum Institut, DK-2300 Copenhagen, Denmark.; Department of Clinical Microbiology, Rigshospitalet, DK-2100 Copenhagen, Denmark.; Department of Clinical Medicine, University of Copenhagen, DK-1165 Copenhagen, Denmark.
Jazyk: angličtina
Zdroj: Journal of fungi (Basel, Switzerland) [J Fungi (Basel)] 2022 Jan 30; Vol. 8 (2). Date of Electronic Publication: 2022 Jan 30.
DOI: 10.3390/jof8020141
Abstrakt: EUCAST has established clinical breakpoints for the six most common Candida species and Cryptococcus neoformans but not for less common yeasts because sufficient evidence is lacking. Consequently, the question "How to interpret the MIC?" for other yeasts often arises. We propose a pragmatic classification for amphotericin B, anidulafungin, fluconazole, and voriconazole MICs against 30 different rare yeasts. This classification takes advantage of MIC data for more than 4000 isolates generated in the EUCAST Development Laboratory for Fungi validated by alignment to published EUCAST MIC data. The classification relies on the following two important assumptions: first, that when isolates are genetically related, pathogenicity and intrinsic susceptibility patterns may be similar; and second, that even if species are not phylogenetically related, the rare yeasts will likely respond to therapy, provided the MIC is comparable to that against wild-type isolates of more prevalent susceptible species because rare yeasts are most likely "rare" due to a lower pathogenicity. In addition, the treatment recommendations available in the current guidelines based on the in vivo efficacy data and clinical experience are taken into consideration. Needless to say, it is of utmost importance (a) to ascertain that the species identification is correct (using MALDI-TOF or sequencing), and (b) to re-test the isolate once or twice to confirm that the MIC is representative for the isolate (because of the inherent variability in MIC determinations). We hope this pragmatic guidance is helpful until evidence-based EUCAST breakpoints can be formally established.
Databáze: MEDLINE
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