检验医学 ›› 2022, Vol. 37 ›› Issue (10): 974-978.DOI: 10.3969/j.issn.1673-8640.2022.010.013

• 技术研究与评价・论著 • 上一篇    下一篇

EUCAST和CLSI微量肉汤稀释法白念珠菌体外药物敏感性试验结果比较

张亚茹1, 凌丽燕1(), 陈敏2   

  1. 1.平湖市第二人民医院检验科,浙江 平湖 314201
    2.海军军医大学第二附属医院皮肤科,上海 200003
  • 收稿日期:2021-10-25 修回日期:2022-01-17 出版日期:2022-10-30 发布日期:2022-11-14
  • 通讯作者: 凌丽燕
  • 作者简介:凌丽燕,E-mail:1144623706@qq.com
    张亚茹,女,1991年生,学士,主管技师,主要从事临床微生物检验工作。
  • 基金资助:
    嘉兴市科学技术局公益性研究计划(2019AY32015);平湖市科技计划项目(平科持〔2020〕28号)

Comparison of EUCAST and CLSI broth microdilution methods for the susceptibility testing against Candida albicans

ZHANG Yaru1, LING Liyan1(), CHEN Min2   

  1. 1. Department of Clinical Laboratory,the Second People's Hospital of Pinghu City,Pinghu 314201,Zhejiang,China
    2. Department of Dermatology,the Second Affiliated Hospital of Naval Military Medical University,Shanghai 200003,China
  • Received:2021-10-25 Revised:2022-01-17 Online:2022-10-30 Published:2022-11-14
  • Contact: LING Liyan

摘要:

目的 比较欧洲抗菌药物敏感性试验委员会(EUCAST)和美国临床实验室标准化协会(CLSI) 微量肉汤稀释法白念珠菌体外药物敏感性试验结果的差异。方法 分别用EUCAST方法和CLSI方法检测42株白念珠菌对两性霉素B、阿尼芬净、卡泊芬净、氟康唑、伊曲康唑、伏立康唑、泊沙康唑和米卡芬净的敏感性,比较2种方法的基本一致性(EA)、分类一致性(CA)、极重大误差率(VME)和重大误差率(ME)。结果 EUCAST方法和CLSI方法总体EA为95.2%~100.0%,CA为95.2%~100.0%,ME为0%~4.8%,VME为0%~2.4%;氟康唑的ME为4.8%,泊沙康唑的VME为2.4%。结论 EUCAST方法和CLSI方法白念珠菌体外药物敏感性试验结果具有可比性,但部分药物之间需要额外的协调步骤。

关键词: 白念珠菌, 微量肉汤稀释法, 体外药物敏感性试验, 欧洲抗菌药物敏感性试验委员会, 美国临床实验室标准化协会

Abstract:

Objective To compare the results of susceptibility testing by European Committee on Antimicrobial Susceptibility Testing(EUCAST) and the Clinical and Laboratory Standards Institute(CLSI) broth microdilution methods against Candida albicans. Methods The susceptibilities of 42 isolates of Candida albicans were determined for amphotericin B,anidulafungin,caspofungin,fluconazole,itraconazole,voriconazole,posaconazole and micafungin according to EUCAST and CLSI methods. The essential agreement(EA),categorical agreement(CA),very major errors(VME) and major errors(ME)of the 2 methods were compared. Results The EA was 95.2%-100.0%. The CA,ME and VWE were 95.2%-100.0%,0%-4.8% and 0%-2.4%,respectively. The ME for fluconazole was 4.8%,and the VME for posaconazole was 2.4%. Conclusions The results of susceptibility testing by EUCAST and CLSI broth microdilution methods are comparable against Candida albicans. There are several areas where additional steps toward harmonization are warranted.

Key words: Candida albicans, Broth microdilution method, In vitro susceptibility testing, European Committee on Antimicrobial Susceptibility Testing, Clinical and Laboratory Standards Institute

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