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首页> 外文期刊>Journal of Clinical Microbiology >Rapid Antifungal Susceptibility Determination for Yeast Isolates by Use of Etest Performed Directly on Blood Samples from Patients with Fungemia
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Rapid Antifungal Susceptibility Determination for Yeast Isolates by Use of Etest Performed Directly on Blood Samples from Patients with Fungemia

机译:通过直接在真菌病患者血液样本上进行的Etest快速测定酵母菌的抗真菌药性

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We prospectively determined the antifungal susceptibility of yeast isolates causing fungemia using the Etest on direct blood samples (195 prospectively collected and 133 laboratory prepared). We compared the Etest direct (24 h of incubation) with CLSI M27-A3 and the standard Etest methodologies for fluconazole, voriconazole, posaconazole, isavuconazole, caspofungin, and amphotericin B. Strains were classified as susceptible, resistant, or nonsusceptible using CLSI breakpoints (voriconazole breakpoints were used for posaconazole and isavuconazole). Categorical errors between Etest direct and CLSI M27-A3 for azoles were mostly minor. No errors were detected for caspofungin, and high percentages of major errors were detected for amphotericin B. For the azoles, false susceptibility (very major errors) was found in only two (0.6%) isolates (Candida tropicalis and C. glabrata). False resistance (major errors) was detected in 46 (14%) isolates for the three azoles (in 23 [7%] after excluding posaconazole). Etest direct of posaconazole yielded a higher number of major errors than the remaining azoles, especially for C. glabrata, Candida spp., and other yeasts. Excluding C. glabrata, Candida spp., and other yeasts, the remaining species did not yield major errors. Etest direct for fluconazole, voriconazole, isavuconazole, and caspofungin shows potential as an alternative to the CLSI M27-A3 procedure for performing rapid antifungal susceptibility tests on yeast isolates from patients with fungemia. Etest direct is a useful tool to screen for the presence of azole-resistant and caspofungin-nonsusceptible strains.
机译:我们使用Etest对直接血液样本(前瞻性收集了195个样本,并为133个实验室准备了样本)前瞻性地确定了引起真菌分离的酵母分离物的抗真菌敏感性。我们将Ctest M27-A3与直接Etest(孵育24小时)以及氟康唑,伏立康唑,泊沙康唑,异氟康唑,卡泊芬净和两性霉素B的标准Etest方法进行了比较。使用CLSI断点将菌株分类为易感,耐药或不敏感(伏立康唑的断点用于泊沙康唑和异氟康唑。 Etest direct和CLSI M27-A3之间的唑类分类错误主要是较小的。卡泊芬净没有发现错误,而两性霉素B却发现了较大百分比的重大错误。对于唑类,只有两个(0.6%)分离株( Candida Tropicalis )发现了假药敏性(非常重大的错误)。和 glabrata )。在三种唑类的46种(14%)分离物中检测到假抗性(重大错误)(排除泊沙康唑后的23种[7%])。直接进行泊沙康唑的Etest生成的主要错误数比其余的唑类要多,尤其是对于 C而言。 glabrata Candida spp。和其他酵母。不包括 C。 glabrata Candida spp。和其他酵母菌,其余物种没有产生重大错误。直接针对氟康唑,伏立康唑,伊沙康康唑和卡泊芬净的Etest显示出替代CLSI M27-A3程序的潜力,该程序可对患有真菌病患者的酵母菌株进行快速抗真菌药敏试验。直接Etest是一种有用的工具,可筛选是否存在对唑类耐药和卡泊芬净不敏感的菌株。

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