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使用Verigene革兰氏阴性血培养核酸检测进行快速检测并联合抗菌药物管理干预以应对革兰氏阴性菌血症。

Rapid testing using the Verigene Gram-negative blood culture nucleic acid test in combination with antimicrobial stewardship intervention against Gram-negative bacteremia.

作者信息

Bork Jacqueline T, Leekha Surbhi, Heil Emily L, Zhao LiCheng, Badamas Rilwan, Johnson J Kristie

机构信息

Department of Medicine, Division of Infectious Diseases, University of Maryland School of Medicine, Baltimore, Maryland, USA

Department of Medicine, Division of Infectious Diseases, University of Maryland School of Medicine, Baltimore, Maryland, USA Department of Public Health and Epidemiology, University of Maryland School of Medicine, Baltimore, Maryland, USA.

出版信息

Antimicrob Agents Chemother. 2015 Mar;59(3):1588-95. doi: 10.1128/AAC.04259-14. Epub 2014 Dec 29.

Abstract

Rapid identification of microorganisms and antimicrobial resistance is paramount for targeted treatment in serious bloodstream infections (BSI). The Verigene Gram-negative blood culture nucleic acid test (BC-GN) is a multiplex, automated molecular diagnostic test for identification of eight Gram-negative (GN) organisms and resistance markers from blood culture with a turnaround time of approximately 2 h. Clinical isolates from adult patients at the University Maryland Medical Center with GN bacteremia from 1 January 2012 to 30 June 2012 were included in this study. Blood culture bottles were spiked with clinical isolates, allowed to incubate, and processed by BC-GN. A diagnostic evaluation was performed. In addition, a theoretical evaluation of time to effective and optimal antibiotic was performed, comparing actual antibiotic administration times from chart review ("control") to theoretical administration times based on BC-GN reporting and antimicrobial stewardship team (AST) review ("intervention"). For organisms detected by the assay, BC-GN correctly identified 95.6% (131/137), with a sensitivity of 97.1% (95% confidence interval [CI], 90.7 to 98.4%) and a specificity of 99.5% (95% CI, 98.8 to 99.8%). CTX-M and OXA resistance determinants were both detected. Allowing 12 h from Gram stain for antibiotic implementation, the intervention group had a significantly shorter duration to both effective (3.3 versus 7.0 h; P < 0.01) and optimal (23.5 versus 41.8 h; P < 0.01) antibiotic therapy. BC-GN with AST intervention can potentially decrease time to both effective and optimal antibiotic therapy in GN BSI.

摘要

快速鉴定微生物及抗菌药物耐药性对于严重血流感染(BSI)的靶向治疗至关重要。Verigene革兰氏阴性血培养核酸检测(BC-GN)是一种用于从血培养中鉴定8种革兰氏阴性(GN)菌及耐药标志物的多重自动化分子诊断检测,周转时间约为2小时。本研究纳入了2012年1月1日至2012年6月30日在马里兰大学医学中心患有GN菌血症的成年患者的临床分离株。将临床分离株接种到血培养瓶中,进行培养,然后用BC-GN进行处理。进行了诊断评估。此外,还对有效和最佳抗生素使用时间进行了理论评估,将病历审查中的实际抗生素给药时间(“对照”)与基于BC-GN报告和抗菌药物管理团队(AST)审查的理论给药时间(“干预”)进行比较。对于该检测方法检测到的微生物,BC-GN正确鉴定率为95.6%(131/137),灵敏度为97.1%(95%置信区间[CI],90.7至98.4%),特异性为99.5%(95%CI,98.8至99.8%)。CTX-M和OXA耐药决定簇均被检测到。从革兰氏染色开始允许12小时实施抗生素治疗,干预组达到有效(3.3小时对7.0小时;P<0.01)和最佳(23.5小时对41.8小时;P<0.01)抗生素治疗的持续时间显著更短。BC-GN联合AST干预可能会缩短GN菌血症中有效和最佳抗生素治疗的时间。

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