Evaluation of the Etest method for determining voriconazole susceptibilities of 312 clinical isolates of Candida species by using three different agar media

Citation
Ma. Pfaller et al., Evaluation of the Etest method for determining voriconazole susceptibilities of 312 clinical isolates of Candida species by using three different agar media, J CLIN MICR, 38(10), 2000, pp. 3715-3717
Citations number
20
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF CLINICAL MICROBIOLOGY
ISSN journal
00951137 → ACNP
Volume
38
Issue
10
Year of publication
2000
Pages
3715 - 3717
Database
ISI
SICI code
0095-1137(200010)38:10<3715:EOTEMF>2.0.ZU;2-9
Abstract
Performance of the Etest for voriconazole susceptibility testing of 312 iso lates of Candida spp, was assessed against that of the National Committee f or Clinical Laboratory Standards (NCCLS) microdilution broth method. The NC CLS method employed RPMI 1640 broth medium, and MICs were read after incuba tion for 48 h at 35 degrees C, Etest MICs were determined with RPMI agar co ntaining 2% glucose (RPG), Casitone agar (CAS), and antibiotic medium 3 (AM 3) agar and were read after incubation for 48 h at 35 degrees C. The Candid a spp, isolates included C, albicans (n = 174), C. glabrata (n = 55), C. tr opicalis (n = 31), C. parapsilosis (n = 39), C. krusei (n = 5), C, lusitani ae (n = 2), and C. guilliermondii (n = 6). The Etest results obtained using RPG correlated well with the reference MICs, Overall agreement ranged from 91% for C. glabrata to 100% for C. tropicalis, C. parapsilosis, C. guillie rmondii, C. krusei, and C, lusitaniae, When CAS was used, agreement ranged from 80% for C, krusei to 100% for C, pampsilosis, C. guilliermondii, and C . lusitaniae, With AM3, agreement ranged from 58% for C, glabrata to 100% f or C. lusitaniae and C, guilliermondii. The Etest method using RPG appears to be a useful method for determining voriconazole susceptibilities of Cand ida species.