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Agreement of Direct Antifungal Susceptibility Testing from Positive Blood Culture Bottles with the Conventional Method for Candida Species

机译:阳性血培养瓶直接抗真菌药敏试验与传统念珠菌属检测方法的协议

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Early availability of antifungal susceptibilities can ensure timely institution of targeted therapy in candidemia, which can improve patient outcomes. This study prospectively determines the agreement between the results of direct testing of antifungal susceptibilities from blood culture bottles by disk diffusion and Etest and the results of standardized susceptibility testing methods; direct testing would allow susceptibility results to be available 1 to 2 days earlier. A total of 104 blood cultures with different Candida species (28% C. albicans, 27% C. parapsilosis, 26% C. tropicalis, etc.) were evaluated between January 2012 and May 2013 for agreement of fluconazole, voriconazole, and amphotericin B susceptibility results by disk diffusion. Agreement in MICs obtained by Etest was determined for fluconazole (21 isolates), voriconazole (28 isolates), amphotericin (29 isolates), and caspofungin (29 isolates). The kappa scores for categorical agreement were highest for fluconazole by disk diffusion (0.902, standard error [SE] = 0.076) and Etest (1.00, SE = 0.218) and for amphotericin B by disk diffusion (1.00, SE = 0.098). The Pearson correlation (r) of zone diameters was strongest for fluconazole (0.69) and amphotericin (0.70) and moderate for voriconazole (0.60), and the Pearson correlation of MICs was strongest for fluconazole (0.94) and caspofungin (0.88). However, the moderate correlation of amphotericin MICs with zone diameters (?0.42) precludes the use of amphotericin B disk diffusion for susceptibility testing. There were no very major errors; however, there were 1 (1%) major and 5 (4.8%) minor errors with disk diffusion and 4 (13.3%) minor errors with Etest. Thus, antifungal disk diffusion directly from blood culture bottles is a rapid and easy method for fluconazole and voriconazole susceptibility testing for timely tailoring of candidemia therapy.
机译:早期可获得的抗真菌药敏性可以确保及时实施针对念珠菌病的靶向治疗,从而可以改善患者的预后。这项研究前瞻性地确定了通过圆盘扩散法和Etest直接从血培养瓶中检测抗真菌药敏性的结果与标准化药敏试验方法的结果之间的一致性;直接测试可以使药敏性结果提前1至2天获得。在2012年1月至2013年5月之间,共评估了104种不同念珠菌属的血液培养物(28%的白色念珠菌,27%的副念珠菌,26%的热带念珠菌等),以确认氟康唑,伏立康唑和两性霉素B的一致性磁盘扩散会导致磁化率下降。确定了通过Etest获得的MIC中的氟康唑(21株),伏立康唑(28株),两性霉素(29株)和卡泊芬净(29株)在MIC中的一致性。碟形扩散法氟康唑的类别分类卡帕评分最高(0.902,标准误[SE] = 0.076)和Etest(1.00,SE = 0.218),两性霉素B碟形扩散的卡帕评分最高(1.00,SE = 0.098)。氟康唑(0.69)和两性霉素(0.70)的区域直径的皮尔森相关性( r )最强,伏立康唑(0.60)的区域直径的皮尔森相关性最强,氟康唑(0.94)和MIC的皮尔逊相关性最强。卡泊芬净(0.88)。但是,两性霉素MIC与区域直径的适度相关性(?0.42)排除了使用两性霉素B盘扩散进行药敏试验的可能性。没有非常大的错误。但是,磁盘扩散的主要错误为1(1%),次要错误为5(4.8%),Etest为4(13.3%)次要错误。因此,直接从血培养瓶中扩散的抗真菌盘是氟康唑和伏立康唑药敏试验的一种快速简便的方法,可及时调整念珠菌血症的治疗方法。

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