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首页> 外文期刊>Journal of Clinical Microbiology >Comparative Evaluation of Etest and Sensititre YeastOne Panels against the Clinical and Laboratory Standards Institute M27-A2 Reference Broth Microdilution Method for Testing Candida Susceptibility to Seven Antifungal Agents
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Comparative Evaluation of Etest and Sensititre YeastOne Panels against the Clinical and Laboratory Standards Institute M27-A2 Reference Broth Microdilution Method for Testing Candida Susceptibility to Seven Antifungal Agents

机译:针对临床和实验室标准协会M27-A2参考肉汤微稀释法测试念珠菌对7种抗真菌药的敏感性,对Etest和Sensititre YeastOne板进行比较评估

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To assess their utility for antifungal susceptibility testing in our clinical laboratory, the Etest and Sensititre methods were compared with the Clinical and Laboratory Standards Institute (CLSI) M27-A2 reference broth microdilution method. Fluconazole (FL), itraconazole (I), voriconazole (V), posaconazole (P), flucytosine (FC), caspofungin (C), and amphotericin B (A) were tested with 212 Candida isolates. Reference MICs were determined after 48 h of incubation, and Etest and Sensititre MICs were determined after 24 h and 48 h of incubation. Overall, excellent essential agreement (EA) between the reference and test methods was observed for Etest (95%) and Sensititre (91%). Etest showed an ≥92% EA for MICs for all drugs tested; Sensititre showed a ≥92% EA for MICs for I, FC, A, and C but 82% for FL and 85% for V. The overall categorical agreement (CA) was 90% for Etest and 88% for Sensititre; minor errors accounted for the majority of all categorical errors for both systems. Categorical agreement was lowest for Candida glabrata and Candida tropicalis with both test systems. Etest and Sensititre provided better CA at 24 h compared to 48 h for C. glabrata; however, CA for C. glabrata was <80% for FL with both test systems despite MIC determination at 24 h. Agreement between technologists for both methods was ≥98% for each agent against all organisms tested. Overall, Etest and Sensititre methods compared favorably with the CLSI reference method for determining the susceptibility of Candida. However, further evaluation of their performance for determining the MICs of azoles, particularly for C. glabrata, is warranted.
机译:为了评估其在我们的临床实验室中进行抗真菌药敏试验的效用,将Etest和Sensititre方法与临床和实验室标准协会(CLSI)M27-A2参考肉汤微量稀释法进行了比较。氟康唑(FL),伊曲康唑(I),伏立康唑(V),泊沙康唑(P),氟胞嘧啶(FC),卡泊芬净(C)和两性霉素B(A)用212个 Candida 分离株进行了测试。孵育48小时后确定参考MIC,孵育24小时和48小时后确定Etest和敏感性MIC。总体而言,对于Etest(95%)和Sensititre(91%),在参考方法和测试方法之间观察到极好的基本一致性(EA)。 Etest对所有受测药物的MIC均显示≥92%的EA;对于I,FC,A和C,Sensititre的MIC的EA≥92%,但对于FL的82%的V,对于V的MIC的EA的≥85%。轻微错误占两个系统所有类别错误的大部分。在这两个测试系统中, glabrata candidatropicis 的类别一致性最低。与 C相比,Etest和Sensititre在24 h提供了更好的CA。 glabrata ;但是, C的CA。尽管在24 h进行MIC测定,两种测试系统的glabrata 均<80%。对于每种试剂,针对所有被测生物,两种方法的技术人员之间的一致性均≥98%。总体而言,Etest和Sensititre方法在确定 Candida 敏感性方面优于CLSI参考方法。但是,需要进一步评估其在确定唑类MIC方面的性能,尤其是对于C。 glabrata 是必要的。

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