Cr. Cooper et Mr. Mcginnis, IN-VITRO SUSCEPTIBILITY OF CLINICAL YEAST ISOLATES TO FLUCONAZOLE ANDTERCONAZOLE, American journal of obstetrics and gynecology, 175(6), 1996, pp. 1626-1631
OBJECTIVE: Fifty clinical yeast isolates, representing equally Candida
albicans, Candida krusei, Candida parapsilosis, Candida tropicalis, a
nd Torulopsis glabrata, were tested in vitro for their susceptibility
to terconazole and fluconazole. STUDY DESIGN: The minimal inhibitory c
oncentrations of terconazole and fluconazole were determined by use of
a proposed standardized broth macrodilution assay. Also, the response
of selected yeast isolates to 25 mu g of either drug was measured by
agarose disk diffusion experiments. RESULTS: For all species the minim
um inhibitory concentrations for terconazole were significantly lower
than those for fluconazole (p < 0.05). In fact, for each individual is
olate the minimum inhibitory concentration of terconazole was consiste
ntly lower than that of fluconazole. Differences in the geometric mean
of terconazole and fluconazole minimum inhibitory concentrations were
largest among C. krusei and T. glabrata, followed by C. parapsilosis,
C. tropicalis, and C. albicans, in order of decreasing difference. Di
sk diffusion experiments suggested that terconazole is a more effectiv
e fungistatic agent than fluconazole is. CONCLUSION: Terconazole may b
e more effective than fluconazole against yeast species other than C.
albicans.