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Antimicrobial Agents and Chemotherapy, June 1999, p. 1463-1464, Vol. 43, No. 6
Department of Medical
Microbiology1 and Faculty of
Pharmacy,3 University of Manitoba, and
Departments of Clinical
Microbiology2 and
Medicine,4 Health Sciences Centre,
Winnipeg, Manitoba, Canada
Received 23 February 1999/Returned for modification 15 March
1999/Accepted 30 March 1999
Fluconazole-resistant Candida albicans and
intrinsically fluconazole-resistant Candida species
have been reported as bloodstream isolates. However, an association
between the isolation of fluconazole-resistant Candida from
the bloodstream and patient risk factors for fungemia has not been
established. The purpose of this study was to determine the prevalence
of fluconazole resistance in bloodstream isolates of
Candida species and Cryptococcus neoformans
collected from patients with neutropenia, one of the most important
risk factors for fungemia. MICs of voriconazole, fluconazole,
itraconazole, ketoconazole, amphotericin B, and flucytosine were
determined by the National Committee for Clinical Laboratory Standards
M27-A method (1997). Voriconazole, on a per-weight basis, was the most active azole tested. Fluconazole resistance (MIC
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
In Vitro Susceptibilities of Candida and
Cryptococcus neoformans Isolates from Blood Cultures of
Neutropenic Patients
64 µg/ml)
was not identified in any of the C. albicans
(n = 513), Candida parapsilosis (n = 78), Candida tropicalis
(n = 62), or C. neoformans
(n = 38) isolates tested.
*
Corresponding author. Department of Clinical
Microbiology, Health Sciences Centre, MS673, 820 Sherbrook St.,
Winnipeg, Manitoba R3A 1R9, Canada. Phone: (204) 787-1191. Fax: (204)
787-4699. E-mail: dhoban{at}hsc.mb.ca.
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