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革兰氏阴性杆菌直接从 BacT/ALERT 阳性血培养瓶中分离培养后,用 Vitek 2 鉴定和药敏试验的比较评估。

Comparative evaluation of Vitek 2 identification and susceptibility testing of Gram-negative rods directly and isolated from BacT/ALERT-positive blood culture bottles.

机构信息

Microbiology Service, University Hospital Virgen de la Arrixaca, El Palmar, Murcia, Spain.

出版信息

Eur J Clin Microbiol Infect Dis. 2012 May;31(5):663-9. doi: 10.1007/s10096-011-1356-1. Epub 2011 Jul 28.

Abstract

The performance of Vitek 2 was evaluated for the identification and susceptibility testing of Gram-negative bacilli directly from positive blood cultures bottles. Direct inoculation of the positive blood cultures with the Vitek cards ID-GN and AST-NO58 was compared with the standard inoculation method based on the sub-culture of the positive blood culture to agar. A total of 142 blood cultures were included in the study; of those, 119 were from patients' clinical samples, while 23 were artificially prepared with strains showing different mechanisms of resistance. A total of 136 (95.8%) strains were correctly identified to the species level, only 2 (1.4%) were mis-identified and 4 (2.8%) were not identified. Susceptibility results were available for all isolates tested against 17 antibiotics, thus, resulting in a total of 2,414 isolate/anti-microbial combinations. The error rate was 2.8% (67/2,414) overall; 0.6% (14/2,414) very major errors, 0.1% (3/2,414) major errors and 2.1% (50/2,414) minor errors. The direct method detected 88.5% (22/25) of the strains producing extended-spectrum beta-lactamases (ESBLs). The susceptibility agreement among the added strains with ESBL, AMPc hyperproduction, resistance to ceftazidime, carbapenems and cefepime was very high. Direct identification and susceptibility testing gave rapid and reliable results, reducing by 24 h the turnaround time of the microbiology laboratory.

摘要

Vitek 2 系统用于直接从阳性血培养瓶中鉴定和药敏检测革兰氏阴性菌的性能评估。将阳性血培养瓶中的直接接种 Vitek 卡 ID-GN 和 AST-NO58 与基于琼脂的阳性血培养物的标准接种方法进行比较。共纳入 142 份血培养物;其中,119 份来自患者的临床样本,23 份为人工制备的具有不同耐药机制的菌株。共有 136 株(95.8%)菌被正确鉴定到种水平,仅 2 株(1.4%)被错误鉴定,4 株(2.8%)未鉴定。对所有分离株进行了 17 种抗生素的药敏试验,因此,共获得了 2414 株分离株/抗菌组合。总的错误率为 2.8%(67/2414);0.6%(14/2414)为非常大误差,0.1%(3/2414)为主要误差,2.1%(50/2414)为次要误差。直接法检测到 25 株产超广谱β-内酰胺酶(ESBLs)菌株中的 88.5%(22/25)。添加的具有 ESBL、AMPc 过度产生、对头孢他啶、碳青霉烯类和头孢吡肟耐药的菌株的药敏一致性非常高。直接鉴定和药敏检测可快速、可靠地得出结果,将微生物实验室的周转时间缩短了 24 小时。

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