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评价 Quantamatrix dRAST 系统与商用 Micronaut 肉汤微量稀释法系统比较,用于快速检测阳性血培养物中的细菌分离物的抗菌药物敏感性。

Evaluation of Quantamatrix dRAST system for rapid antimicrobial susceptibility testing of bacterial isolates from positive blood cultures, in comparison with commercial Micronaut broth microdilution system.

机构信息

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; Microbiology and Virology Unit, Careggi University Hospital, Florence, Italy.

出版信息

Diagn Microbiol Infect Dis. 2024 Sep;110(1):116436. doi: 10.1016/j.diagmicrobio.2024.116436. Epub 2024 Jul 11.

Abstract

Antimicrobial susceptibility testing (AST) from blood culture (BC) may take several days, limiting the eventual impact on antimicrobial stewardship. Hence, rapid AST systems represent a valuable support in shorting the time-to-response. In this work, the Quantamatrix dRAST system (dRAST) was evaluated for rapid AST on 100 monomicrobial BCs (50 Gram-negatives and 50 Gram-positives), including several isolates with clinically relevant resistance mechanisms. AST results were provided in 6-hours, on average. Compared to Micronaut (Merlin) system based on broth microdilution, dRAST exhibited an overall categorical agreement of 92.5 %, essential agreement of 89.0 %, and mean bias of 15.9 %. Category overestimation (potentially leading to unnecessary high-dosage treatment or to exclude active agents) and category underestimation (potentially leading to underdosing or using ineffective agents) were observed in 4.3 % and 3.1 % of cases, respectively. Even though several issues were reported, results confirmed the potential contribution of dRAST to shorten the BCs clinical microbiology workflow and management.

摘要

血培养(BC)的抗菌药物敏感性测试(AST)可能需要数天时间,这限制了其对抗菌药物管理的最终影响。因此,快速 AST 系统在缩短反应时间方面具有重要的支持作用。在这项工作中,评估了 Quantamatrix dRAST 系统(dRAST)对 100 株单一致病菌 BC(50 株革兰氏阴性菌和 50 株革兰氏阳性菌)的快速 AST,包括几种具有临床相关耐药机制的分离株。AST 结果平均在 6 小时内提供。与基于肉汤微量稀释的 Micronaut(Merlin)系统相比,dRAST 的总体分类一致性为 92.5%,基本一致性为 89.0%,平均偏差为 15.9%。分别有 4.3%和 3.1%的病例出现了分类高估(可能导致不必要的高剂量治疗或排除有效药物)和分类低估(可能导致剂量不足或使用无效药物)。尽管报告了一些问题,但结果证实了 dRAST 有潜力缩短 BC 临床微生物学工作流程和管理。

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