Pfaller M A, Boyken L, Hollis R J, Messer S A, Tendolkar S, Diekema D J
Department of Pathology, Roy J. and Lucille A. Carver College of Medicine,University of Iowa, Iowa City, IA, USA.
Diagn Microbiol Infect Dis. 2004 Oct;50(2):113-7. doi: 10.1016/j.diagmicrobio.2004.06.013.
A commercially prepared dried-broth microdilution panel (Sensititre, TREK Diagnostic Systems, Cleveland, OH) was compared with a reference frozen-broth microdilution panel for antifungal susceptibility testing of 728 clinical isolates of Candida spp. and 98 clinical isolates of Cryptococcus neoformans. The antifungal agents tested were amphotericin B, fluconazole, 5-fluorocytosine (5FC), itraconazole, and voriconazole. Microdilution testing was performed according to NCCLS recommendations. Minimum inhibitory concentration (MIC) endpoints were read visually after 48 hours of incubation (72 hours for C. neoformans) and were assessed independently for each microdilution panel. Discrepancies among MIC endpoints of no more than 2 log(2) dilutions were used to calculate the percentage of agreement. Overall levels of agreement between the study and reference panels were 98% for Candida spp. and 93% for C. neoformans. The agreement for each antifungal agent ranged from 96.6% for voriconazole to 99.4% for amphotericin B. The TREK dried microdilution panel appears to be a viable alternative to frozen-broth microdilution panels for testing of Candida spp. and C. neoformans.
将一种市售的干肉汤微量稀释板(Sensititre,TREK诊断系统公司,俄亥俄州克利夫兰)与一种用于念珠菌属728株临床分离株和新型隐球菌98株临床分离株抗真菌药敏试验的参考冷冻肉汤微量稀释板进行比较。所测试的抗真菌药物为两性霉素B、氟康唑、5-氟胞嘧啶(5FC)、伊曲康唑和伏立康唑。微量稀释试验按照美国国家临床实验室标准委员会(NCCLS)的建议进行。孵育48小时后(新型隐球菌为72小时)目视读取最低抑菌浓度(MIC)终点,并对每个微量稀释板独立评估。MIC终点之间相差不超过2个对数(2)稀释度用于计算符合率。研究板和参考板之间的总体符合率念珠菌属为98%,新型隐球菌为93%。每种抗真菌药物的符合率范围从伏立康唑的96.6%到两性霉素B的99.4%。对于念珠菌属和新型隐球菌的检测,TREK干微量稀释板似乎是冷冻肉汤微量稀释板的一种可行替代方法。