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QMAC-dRAST V2.0 系统用于革兰氏阴性血培养分离物快速抗生素药敏试验的比较评估。

Comparative evaluation of the QMAC-dRAST V2.0 system for rapid antibiotic susceptibility testing of Gram-negative blood culture isolates.

机构信息

Microbiology department, Georges Pompidou European Hospital, AP-HP-Centre Université de Paris, Université de Paris, Paris, France.

Microbiology department, Georges Pompidou European Hospital, AP-HP-Centre Université de Paris, Université de Paris, Paris, France.

出版信息

J Microbiol Methods. 2020 May;172:105902. doi: 10.1016/j.mimet.2020.105902. Epub 2020 Mar 20.

DOI:10.1016/j.mimet.2020.105902
PMID:32205178
Abstract

To comparatively evaluate the performance of the rapid antimicrobial susceptibility testing (AST) system QMAC-dRAST V2.0 and of standard disk diffusion in agar, AST was performed directly from 100 positive blood culture bottles with Gram-negative bacilli. AST results provided by QMAC-dRAST showed 92.9% agreement with disk diffusion method results. Discrepancies observed between results obtained with QMAC-dRAST and disk diffusion method conducted to 10 very major errors (0.8%, S with QMAC-dRAST vs R with disk diffusion method), 40 major errors (3.2%, R vs S, respectively), 15 minor errors (1.2%, S vs I or I vs R, respectively) and 23 very minors errors (1.8%, I vs S or R vs I, respectively). For very major and major errors, in only 36% of the cases did the repeat QMAC-dRAST confirm the initial result, whereas a repeat AST using disk diffusion method confirmed the initial result in 92% of cases. AST results obtained using microdilution in liquid medium confirmed those obtained with QMAC-dRAST and disk diffusion method in 4% and 89%, respectively. Repeatability and reproducibility tests performed on QMAC-dRAST using reference strains showed 94% to 100% of R/S/I categorical agreement.

摘要

为了比较快速抗菌药敏检测(AST)系统 QMAC-dRAST V2.0 和标准琼脂扩散法的性能,我们直接对 100 瓶革兰氏阴性菌阳性血培养瓶进行了 AST。QMAC-dRAST 提供的 AST 结果与琼脂扩散法结果的符合率为 92.9%。用 QMAC-dRAST 和琼脂扩散法进行的 AST 结果与 10 个非常大误差(0.8%,用 QMAC-dRAST 表示的 S 与用琼脂扩散法表示的 R)、40 个大误差(3.2%,分别为 R 和 S)、15 个小误差(1.2%,分别为 S 和 I 或 I 和 R)和 23 个非常小误差(1.8%,分别为 I 和 S 或 R 和 I)观察到差异。对于非常大误差和大误差,只有 36%的情况下,重复 QMAC-dRAST 确认了初始结果,而用琼脂扩散法重复 AST 确认初始结果的比例为 92%。用液体培养基进行微量稀释法获得的 AST 结果与 QMAC-dRAST 和琼脂扩散法的符合率分别为 4%和 89%。用参考菌株对 QMAC-dRAST 进行的重复性和再现性测试显示,R/S/I 分类一致性为 94%至 100%。

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