VCU Medical Center, Richmond, Virginia, USA.
Antimicrob Agents Chemother. 2011 Nov;55(11):5150-4. doi: 10.1128/AAC.00686-11. Epub 2011 Aug 29.
Although clinical breakpoints have not been established for mold testing, epidemiological cutoff values (ECVs) are available for Aspergillus spp. versus the triazoles and caspofungin. Wild-type (WT) MIC distributions (organisms in a species-drug combination with no acquired resistance mechanisms) were defined in order to establish ECVs for six Aspergillus spp. and amphotericin B. Two sets (CLSI/EUCAST broth microdilution) of available MICs were evaluated: those for A. fumigatus (3,988/833), A. flavus (793/194), A. nidulans (184/69), A. niger (673/140), A. terreus (545/266), and A. versicolor (135/22). Three sets of data were analyzed: (i) CLSI data gathered in eight independent laboratories in Canada, Europe, and the United States; (ii) EUCAST data from a single laboratory; and (iii) the combined CLSI and EUCAST data. ECVs, expressed in μg/ml, that captured 95%, 97.5%, and 99% of the modeled wild-type population (CLSI and combined data) were as follows: for A. fumigatus, 2, 2, and 4; for A. flavus, 2, 4, and 4; for A. nidulans, 4, 4, and 4; for A. niger, 2, 2, and 2; for A. terreus, 4, 4, and 8; and for A. versicolor, 2, 2, and 2. Similar to the case for the triazoles and caspofungin, amphotericin B ECVs may aid in the detection of strains with acquired mechanisms of resistance to this agent.
虽然尚未建立用于霉菌检测的临床折点,但已有曲霉菌属与三唑类和卡泊芬净的流行病学切点值(ECV)。为了确定六种曲霉菌属和两性霉素 B 的 ECV,定义了野生型(WT)MIC 分布(在无获得性耐药机制的种-药物组合中的生物体)。评估了两套(CLSI/EUCAST 肉汤微量稀释法)可用 MIC:用于烟曲霉(3,988/833)、黄曲霉(793/194)、构巢曲霉(184/69)、黑曲霉(673/140)、土曲霉(545/266)和彩绒革盖菌(135/22)的 MIC。分析了三组数据:(i)在加拿大、欧洲和美国的八个独立实验室中收集的 CLSI 数据;(ii)来自单个实验室的 EUCAST 数据;以及(iii)CLSI 和 EUCAST 合并数据。以 μg/ml 表示的捕获了 95%、97.5%和 99%模型野生型群体(CLSI 和合并数据)的 ECV 如下:对于烟曲霉,分别为 2、2 和 4;对于黄曲霉,分别为 2、4 和 4;对于构巢曲霉,分别为 4、4 和 4;对于黑曲霉,分别为 2、2 和 2;对于土曲霉,分别为 4、4 和 8;对于彩绒革盖菌,分别为 2、2 和 2。与三唑类和卡泊芬净的情况类似,两性霉素 B 的 ECV 可能有助于检测对该药物具有获得性耐药机制的菌株。