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在ARTEMIS DISK全球抗真菌监测项目中,对念珠菌属进行氟康唑和伏立康唑纸片扩散试验的结果与一家中央参考实验室的结果比较。

Comparison of results of fluconazole and voriconazole disk diffusion testing for Candida spp. with results from a central reference laboratory in the ARTEMIS DISK Global Antifungal Surveillance Program.

作者信息

Pfaller Michael A, Boyken Linda, Hollis Richard J, Kroeger Jennifer, Messer Shawn A, Tendolkar Shailesh, Diekema Daniel J

机构信息

Department of Pathology, University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.

出版信息

Diagn Microbiol Infect Dis. 2009 Sep;65(1):27-34. doi: 10.1016/j.diagmicrobio.2009.05.007.

Abstract

The accuracy of antifungal susceptibility testing is important for reliable resistance surveillance and for the clinical management of patients with serious infections due to Candida spp. Our primary objective was to compare the results of fluconazole and voriconazole disk diffusion testing of 3227 Candida spp. performed by 47 centers participating in the ARTEMIS program with disk diffusion and MIC results obtained by the central reference laboratory. The overall categoric agreement between participant disk diffusion test results and reference MIC results was 87% for fluconazole and 95.2% for voriconazole. Likewise good agreement was observed between participant disk diffusion test results and reference laboratory disk diffusion test results, with an agreement of 90.5%, 1% very major error (VME), and 3.4% major error (ME) for fluconazole and 94.2%, 1.1% VME, and 2.5% ME for voriconazole. The disk diffusion test was reliable for detecting those isolates of Candida spp. that were characterized as resistant to fluconazole and voriconazole by MIC testing. External quality assurance data obtained by surveillance programs such as the ARTEMIS Global Antifungal Surveillance Program ensure the generation of useful surveillance data and result in the continued improvement of antifungal susceptibility testing protocols.

摘要

抗真菌药敏试验的准确性对于可靠的耐药性监测以及念珠菌属所致严重感染患者的临床管理至关重要。我们的主要目标是比较参与ARTEMIS项目的47个中心对3227株念珠菌属进行氟康唑和伏立康唑纸片扩散试验的结果与中央参考实验室获得的纸片扩散试验和最低抑菌浓度(MIC)结果。参与者纸片扩散试验结果与参考MIC结果之间的总体分类一致性,氟康唑为87%,伏立康唑为95.2%。同样,在参与者纸片扩散试验结果与参考实验室纸片扩散试验结果之间也观察到良好的一致性,氟康唑的一致性为90.5%,非常主要错误(VME)为1%,主要错误(ME)为3.4%;伏立康唑的一致性为94.2%,VME为1.1%,ME为2.5%。纸片扩散试验对于检测那些通过MIC试验被鉴定为对氟康唑和伏立康唑耐药的念珠菌属菌株是可靠的。通过ARTEMIS全球抗真菌监测项目等监测计划获得的外部质量保证数据确保了有用监测数据的产生,并导致抗真菌药敏试验方案的持续改进。

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