Performance evaluation of the Specific Reveal system for rapid antibiotic susceptibility testing from positive blood cultures containing Gram-negative pathogens.

IF 6.1 2区 医学 Q1 MICROBIOLOGY
Greta Ostermann, Barbara Körber-Irrgang, Alexander Krüger, Pragya Singh, Kenny Vo, Jörg Gielen, Ute Aurbach, Hilmar Wisplinghoff, Nathalie Jazmati
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Abstract

Rapid antimicrobial drug administration is crucial for the efficient treatment of sepsis or septic shock, but empirical therapy is limited by the increasing prevalence of multidrug-resistant bacteria. Thus, rapid and reliable antimicrobial susceptibility testing (AST) is needed to start appropriate antimicrobial drug administration as quickly as possible. In the present study, we evaluated the performance of the Reveal rapid AST system. From February to April 2021, 102 positive blood culture bottles (BCBs) from hospitalized patients with bacteremia caused by Gram-negative bacteria were included in the study. All isolates were tested by the Reveal system directly from the positive BCBs in comparison to the DxM MicroScan WalkAway. Essential agreement (EA) and category agreement (CA) were high with 98.5% and 97.1%, respectively. We also determined the susceptibility of 10 highly resistant CDC & FDA AR strains in duplicate. Here, EA was 99.6% and CA 97.9%. The average time to result by Reveal was 5.4 h ± 1.2 h compared to an average of 16 h by DxM MicroScan WalkAway for clinical strains and 3.8 h ± 1.2 h for more resistant CDC & FDA AR strains. Susceptibility determination with the Reveal rapid AST system directly from positive BCBs is for the frequently represented bug-drug combinations a reliable and accurate approach, meeting the European ISO guideline for the performance of AST systems. Moreover, AST directly from blood cultures performed with the Reveal system saves time when compared to the conventional AST, as no subculturing is needed and time to result is very short.

从含有革兰氏阴性病原体的阳性血液培养物中快速检测抗生素敏感性的 Specific Reveal 系统性能评估。
快速使用抗菌药物对有效治疗脓毒症或脓毒性休克至关重要,但由于耐多药细菌的日益流行,经验疗法受到了限制。因此,需要进行快速、可靠的抗菌药物敏感性检测(AST),以便尽快开始适当的抗菌药物治疗。在本研究中,我们评估了 Reveal 快速 AST 系统的性能。从 2021 年 2 月到 4 月,共有 102 例由革兰氏阴性菌引起的菌血症住院患者的血培养瓶(BCB)检测结果呈阳性。所有分离菌株均由 Reveal 系统直接从阳性 BCB 中进行检测,并与 DxM MicroScan WalkAway 进行比较。基本一致度(EA)和类别一致度(CA)分别为98.5%和97.1%。我们还对 10 株高度耐药的 CDC 和 FDA AR 菌株进行了一式两份的药敏测定。其中,EA 为 99.6%,CA 为 97.9%。用 Reveal 测定结果的平均时间为 5.4 小时 ± 1.2 小时,而用 DxM MicroScan WalkAway 测定临床菌株的平均时间为 16 小时,测定耐药性更强的 CDC 和 FDA AR 菌株的平均时间为 3.8 小时 ± 1.2 小时。使用 Reveal 快速 AST 系统直接从阳性 BCB 进行药敏测定,对于常见的虫-药组合是一种可靠而准确的方法,符合欧洲 ISO AST 系统性能指南的要求。此外,与传统 AST 相比,使用 Reveal 系统直接从血液培养物中进行 AST 可节省时间,因为不需要进行亚培养,而且得出结果的时间非常短。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
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