首页> 外文期刊>Clinical microbiology and infection: European Society of Clinical Microbiology and Infectious Diseases >Multicenter evaluation of the reproducibility of the proposed antifungal susceptibility testing method for fermentative yeasts of the Antifungal Susceptibility Testing Subcommittee of the European Committee on Antimicrobial Susceptibility Testing (AF
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Multicenter evaluation of the reproducibility of the proposed antifungal susceptibility testing method for fermentative yeasts of the Antifungal Susceptibility Testing Subcommittee of the European Committee on Antimicrobial Susceptibility Testing (AF

机译:欧洲抗菌药物敏感性试验委员会(AF)抗真菌药物敏感性试验小组委员会针对发酵酵母提出的抗真菌药物敏感性试验方法的可重复性的多中心评估

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OBJECTIVE: To evaluate the intra- and inter-laboratory reproducibility of a new standard for susceptibility testing of fermentative yeasts. This standard is based on the M27-A procedure of the National Committee for Clinical Laboratory Standards (NCCLS), but incorporates several modifications, including spectrophotometric growth-dependent endpoint reading. METHODS: Nine laboratories participated in the study. Common material lots were used to test six Candida species (one each of C. albicans, C. tropicalis, C. parapsilosis, C. glabrata, C. krusei, and C. lusitaniae), and two quality control strains (C. krusei ATCC6258 and C. parapsilosis ATCC22019). Triplicate testing on three separate days was performed in microtiter format with RPMI-2% glucose, pH 7.0. Flucytosine, fluconazole and itraconazole were tested. In total, 3888 MIC values were included in the analyses. Reproducibility was calculated by means of agreement (percentage of MICs within one two-fold dilution of the mode) and intraclass correlation coefficient (ICC, maximum value of 1). RESULTS: The average intra-laboratory agreements were 99% and 96% after 24 h and 48 h of incubation, respectively, with ICCs of 0.98 and 0.97 (P < 0.05). Two strains exhibiting a trailing effect showed intra-laboratory agreement of 92% and ICCs of < 0.91 at 48 h. The inter-laboratory agreement was 94% and 88% after 24 h and 48 h, respectively, with ICCs of 0.93 and 0.91 (P < 0.05). Lower values of agreement and ICCs were obtained for strains exhibiting trailing after 48 h of incubation. Itraconazole yielded the lowest values of reproducibility. CONCLUSION: The new procedure of EUCAST for antifungal susceptibility testing is a reproducible method within and between laboratories and offers several advantages over the NCCLS approved method.
机译:目的:评价新标准的发酵酵母敏感性试验的实验室内和实验室间可重复性。该标准基于美国国家临床实验室标准委员会(NCCLS)的M27-A程序,但结合了一些修改,包括分光光度法生长依赖性终点读数。方法:九个实验室参加了这项研究。常用材料批次用于测试六种假丝酵母菌(白念珠菌,热带念珠菌,近缘念珠菌,光滑念珠菌,克鲁斯菌和卢氏念珠菌各一种)和两种质量控制菌株(克鲁斯菌ATCC6258)和C. parapsilosis(ATCC22019)。使用RPMI-2%葡萄糖,pH 7.0,以微量滴定形式在三天内进行一式三份测试。测试了氟胞嘧啶,氟康唑和伊曲康唑。分析中总共包括3888个MIC值。通过一致性(模式的两倍稀释内的MIC百分比)和组内相关系数(ICC,最大值为1)计算可重复性。结果:孵育24 h和48 h后,平均实验室内一致性分别为99%和96%,ICC分别为0.98和0.97(P <0.05)。表现出拖尾作用的两个菌株在48 h时的实验室内一致性为92%,ICCs <0.91。实验室间一致性在24 h和48 h后分别为94%和88%,ICC为0.93和0.91(P <0.05)。孵育48小时后出现拖尾的菌株获得较低的协议和ICC值。伊曲康唑的再现性最低。结论:EUCAST的抗真菌药敏试验新程序是实验室内部和实验室之间的可重现方法,与NCCLS批准的方法相比具有许多优点。

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