首页> 美国卫生研究院文献>Journal of Clinical Microbiology >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
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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

机译:EUCAST和CLSI M27-A2肉汤微量稀释法对念珠菌敏感性的国际和多中心比较。氟康唑伊曲康唑泊沙康唑和伏立康唑

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摘要

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.
机译:这项研究的目的是比较欧洲抗生素敏感性试验委员会(EUCAST)和CLSI(以前的NCCLS)方法在六个15个念珠菌白色念珠菌(5个氟康唑-氟喹唑-氟喹诺酮)中获得的氟康唑,伊曲康唑,泊沙康唑和伏立康唑的MIC值。抗性和4个易感剂量依赖性[S-DD]分离株),10达比利尼梭菌,7 C. glabrata(2个耐氟康唑的菌株),5 C guilliermondii(2个耐氟康唑的菌株),10 C. krusei, 9个lusitaniae,10 C. parapsilosis和5 C.tropicis(1个耐氟康唑的分离株)分离株。分别在24和48 h处获得CLSI MIC,在24 h处获得分光光度法EUCAST MIC。方法之间的一致性(在3倍稀释范围内)取决于物种,药物和孵育时间,并且由于EUCAST低于CLSI MIC:总体而言,氟康唑和伏立康唑占94%至95%,泊沙康唑和伊曲康唑占90%至91%将EUCAST MIC与24小时CLSI结果进行了比较。与48小时CLSI端点相比,该协议较低(85%至94%)。每种方法的整体实验室间重现性≥92%。当基于CLSI断点分类进行比较时,包括耐氟康唑和S-DD分离物在内的四个物种中,三个的一致率为68%至76%。在耐氟康唑的菌株中观察到9%的非常重大差异(≤8μg/ ml对≥64μg/ ml)和50%伏立康唑(≤1μg/ ml对≥4μg/ ml)。在评估的八种物种中,伊曲康唑观察到了相似的结果(分类一致性为28%至77%)。对于这些分离物中的一些,泊沙康唑EUCAST MIC也显着低于CLSI MIC模式(0.008至1μg/ ml对1至≥8μg/ ml)。因此,不应将CLSI断点用于解释EUCAST MIC数据。

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