In vitro activities of voriconazole, fluconazole, and itraconazole against566 clinical isolates of Cryptococcus neoformans from the United States and Africa

Citation
Ma. Pfaller et al., In vitro activities of voriconazole, fluconazole, and itraconazole against566 clinical isolates of Cryptococcus neoformans from the United States and Africa, ANTIM AG CH, 43(1), 1999, pp. 169-171
Citations number
24
Categorie Soggetti
Microbiology
Journal title
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
ISSN journal
00664804 → ACNP
Volume
43
Issue
1
Year of publication
1999
Pages
169 - 171
Database
ISI
SICI code
0066-4804(199901)43:1<169:IVAOVF>2.0.ZU;2-7
Abstract
We investigated the in vitro activity of voriconazole compared to those of fluconazole and itraconazole against 566 clinical isolates of Cryptococcus neoformans from Africa (164) and the United States (402). Isolates were obt ained from cerebrospinal fluid (362), blood (139), and miscellaneous sites (65). Voriconazole (MIC at which 90% of the isolates are inhibited [MIC90], 0.12 to 0.25 mu g/ml) was more active than either itraconazole (MIC90, 0.5 mu g/ml) or fluconazole (MIC90, 8.0 to 16 mu g/ml) against both African an d U.S. isolates. Isolates inhibited by greater than or equal to 16 mu g of fluconazole per ml were almost all (99%) inhibited by less than or equal to 1 mu g of voriconazole per ml These results suggest that voriconazole may be useful in the treatment of cryptococcosis.