With the emergence of fungi as important nosocomial pathogens, increas
ing reports of antifungal resistance, and expanding drug therapy optio
ns, the need for clinically relevant antifungal susceptibility testing
is evident. Over the last decade, the National Committee for Clinical
Laboratory Standards (NCCLS) worked to standardize procedures for in
vitro susceptibility testing of Candida species against fluconazole, i
traconazole, 5-fluorocytosine, and amphotericin B. With the establishm
ent of a reproducible methodology, correlation of antifungal susceptib
ility in vitro with clinical outcome is a priority. The NCCLS proposed
susceptibility breakpoints for the three agents against Candida speci
es, with breakpoints for amphotericin B forthcoming. These breakpoints
could provide useful guidance in some clinical situations involving a
zole or S-fluorocytosine therapy; however, routine susceptibility test
ing of fungal isolates should be discouraged.