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在ARTEMIS全球抗真菌监测项目中,将念珠菌属的氟康唑纸片扩散法检测结果与一家中央参考实验室的结果进行比较。

Comparison of results of fluconazole disk diffusion testing for Candida species with results from a central reference laboratory in the ARTEMIS global antifungal surveillance program.

作者信息

Pfaller M A, Hazen K C, Messer S A, Boyken L, Tendolkar S, Hollis R J, Diekema D J

机构信息

Department of Pathology, Roy J. and Lucille A. Carver College of Medicin and College of Public Health, University of Iowa College of Medicine, Iowa City, IA 52242, USA.

出版信息

J Clin Microbiol. 2004 Aug;42(8):3607-12. doi: 10.1128/JCM.42.8.3607-3612.2004.

Abstract

The accuracy of antifungal susceptibility tests is important for accurate resistance surveillance and for the clinical management of patients with serious infections. Our main objective was to compare the results of fluconazole disk diffusion testing of Candida spp. performed by ARTEMIS participating centers with disk diffusion and MIC results obtained by the central reference laboratory. A total of 2,949 isolates of Candida spp. were tested by NCCLS disk diffusion and reference broth microdilution methods in the central reference laboratory. These results were compared to the results of disk diffusion testing performed in the 54 participating centers. All tests were performed and interpreted following NCCLS recommendations. Overall categorical agreement between participant disk diffusion test results and reference laboratory MIC results was 87.4%, with 0.2% very major errors (VME) and 3.3% major errors (ME). The categorical agreement between the disk diffusion test results obtained in the reference laboratory with the MIC test results was similar: 92.8%. Likewise, good agreement was observed between participant disk diffusion test results and reference laboratory disk diffusion test results: 90.4%, 0.4% VME, and 3.4% ME. The disk diffusion test was especially reliable in detecting those isolates of Candida spp. that were characterized as resistant by reference 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 practices.

摘要

抗真菌药敏试验的准确性对于准确的耐药监测以及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ARTEMIS参与中心进行的念珠菌属氟康唑纸片扩散试验结果与中央参考实验室获得的纸片扩散试验和MIC结果。中央参考实验室采用NCCLS纸片扩散法和参考肉汤微量稀释法对总共2949株念珠菌属菌株进行了检测。将这些结果与54个参与中心进行的纸片扩散试验结果进行比较。所有试验均按照NCCLS的建议进行操作和判读。参与中心纸片扩散试验结果与参考实验室MIC结果的总体分类一致性为87.4%,非常重大误差(VME)为0.2%,重大误差(ME)为3.3%。参考实验室获得的纸片扩散试验结果与MIC试验结果之间的分类一致性相似:92.8%。同样,参与中心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:90.4%,VME为0.4%,ME为3.4%。纸片扩散试验在检测那些经参考MIC试验鉴定为耐药性的念珠菌属菌株时特别可靠。通过ARTEMIS全球抗真菌监测计划等监测项目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实践的持续改进。

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