BS EN ISO 16256:2012 PDF

Clinical laboratory testing and in vitro diagnostic test systems. Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases

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BS EN ISO 16256:2012

Clinical laboratory testing and in vitro diagnostic test systems. Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases

Статус документа:: Отменён
Формат:: Электронный (PDF)
Дата публикации:: 31 декабря 2012 г.
ICS:: 11.100.10
Технический комитет:: CEN
SKU:: BS EN ISO 16256:2012

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Abstract

1 Scope This International Standard describes a method for testing the susceptibility to antifungal agents of yeasts, including Candida spp. and Cryptococcus neoformans, that cause infections. The reference method described here has not been used in studies of the yeast forms of dimorphic fungi, such as B. dermatitidis and/or H. capsulatum variety capsulatum . Moreover, testing filamentous fungi (moulds) introduces several additional problems in standardization not addressed by the current procedure. Reference methods for broth dilution antifungal susceptibility testing of filamentous fungi have been developed and are now available as CLSI document M38 and EUCAST document E.DEF 9.1 [4] [5] [6] [7] [8] . This International Standard describes the broth microdilution reference method which can be implemented by either of two pathways. One pathway involves visual determination of MICs (CLSI method) [1] ; the second pathway involves spectrophotometric determination of MICs (EUCAST method) [2] . The MIC reflects the activity of the drug under the described test conditions and can be interpreted for clinical management purposes by taking into account other factors, such as drug pharmacology or antifungal resistance mechanisms. MICs can be categorized as “ susceptible ” (S), “ susceptible dose-dependent” ( S-DD ), “ intermediate ” (I), “non- susceptible ” ( ...

BS EN ISO 16256:2012 PDF

Abstract

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