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Journal of Clinical Microbiology, August 2005, p. 3884-3889, Vol. 43, No. 8
0095-1137/05/$08.00+0 doi:10.1128/JCM.43.8.3884-3889.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
International and Multicenter Comparison of EUCAST and CLSI M27-A2 Broth Microdilution Methods for Testing Susceptibilities of Candida spp. to Fluconazole, Itraconazole, Posaconazole, and Voriconazole
A. Espinel-Ingroff,1*
F. Barchiesi,2
M. Cuenca-Estrella,3
M. A. Pfaller,4
M. Rinaldi,5
J. L. Rodriguez-Tudela,3 and
P. E. Verweij6
VCU Medical Center, Richmond, Virginia,1
Public Health, Ancona, Italy,2
Instituto de Salud Carlos III, Majadahonda, Spain,3
University of Iowa College of Medicine, Iowa City, Iowa,4
University of Texas Health Science Center, San Antonio, Texas,5
Medical Center Nijmegen, Nijmegen, The Netherlands6
Received 14 February 2005/
Returned for modification 11 April 2005/
Accepted 20 May 2005
The aim of this study was to compare MICs of fluconazole, itraconazole, posaconazole, and voriconazole obtained by the European Committee on Antibiotic Susceptibility Testing (EUCAST) and CLSI (formerly NCCLS) methods in each of six centers for 15 Candida albicans (5 fluconazole-resistant and 4 susceptible-dose-dependent [S-DD] isolates), 10 C. dubliniensis, 7 C. glabrata (2 fluconazole-resistant isolates), 5 C. guilliermondii (2 fluconazole-resistant isolates), 10 C. krusei, 9 C. lusitaniae, 10 C. parapsilosis, and 5 C. tropicalis (1 fluconazole-resistant isolate) isolates. CLSI MICs were obtained visually at 24 and 48 h and spectrophotometric EUCAST MICs at 24 h. The agreement (within a 3-dilution range) between the methods was species, drug, and incubation time dependent and due to lower EUCAST than CLSI MICs: overall, 94 to 95% with fluconazole and voriconazole and 90 to 91% with posaconazole and itraconazole when EUCAST MICs were compared against 24-h CLSI results. The agreement was lower (85 to 94%) against 48-h CLSI endpoints. The overall interlaboratory reproducibility by each method was
92%. When the comparison was based on CLSI breakpoint categorization, the agreement was 68 to 76% for three of the four species that included fluconazole-resistant and S-DD isolates; 9% very major discrepancies (
8 µg/ml versus
64 µg/ml) were observed among fluconazole-resistant isolates and 50% with voriconazole (
1 µg/ml versus
4 µg/ml). Similar results were observed with itraconazole for seven of the eight species evaluated (28 to 77% categorical agreement). Posaconazole EUCAST MICs were also substantially lower than CLSI MIC modes (0.008 to 1 µg/ml versus 1 to
8 µg/ml) for some of these isolates. Therefore, the CLSI breakpoints should not be used to interpret EUCAST MIC data.
* Corresponding author. Mailing address: VCU Medical Center, Medical Mycology Research Laboratory, 1101 E. Marshall St., Sanger Hall Room 7049, P. O. Box 980049, Richmond, VA 23298-0049. Phone: (804) 828-9711. Fax: (804) 828-3097. E-mail:
avingrof{at}hsc.vcu.edu.
Journal of Clinical Microbiology, August 2005, p. 3884-3889, Vol. 43, No. 8
0095-1137/05/$08.00+0 doi:10.1128/JCM.43.8.3884-3889.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
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