Department of Laboratory Medicine and Research Institute of Bacterial Resistance, Yonsei University College of Medicine, Seoul, Korea.
Department of Laboratory Medicine, National Cancer Center, Goyang, Korea.
Ann Lab Med. 2018 May;38(3):235-241. doi: 10.3343/alm.2018.38.3.235.
Early and appropriate antibiotic treatment improves the clinical outcome of patients with septicemia; therefore, reducing the turn-around time for identification (ID) and antimicrobial susceptibility test (AST) results is essential. We established a method for rapid ID and AST using short-term incubation of positive blood culture broth samples on solid media, and evaluated its performance relative to that of the conventional method using two rapid ID systems and a rapid AST method.
A total of 254 mono-microbial samples were included. Positive blood culture samples were incubated on blood agar plates for six hours and identified by the MicroFlex LT (Bruker Daltonics) and Vitek-MS (bioMeriéux) systems, followed by AST using the Vitek2 System (bioMeriéux).
The correct species-level ID rates were 82.3% (209/254) and 78.3% (199/254) for the MicroFlex LT and Vitek-MS platforms, respectively. For the 1,174 microorganism/antimicrobial agent combinations tested, the rapid AST method showed total concordance of 97.8% (1,148/1,174) with the conventional method, with a very major error rate of 0.5%, major error rate of 0.7%, and minor error rate of 1.0%.
Routine implementation of this short-term incubation method could provide ID results on the day of blood culture-positivity detection and one day earlier than the conventional AST method. This simple method will be very useful for rapid ID and AST of bacteria from positive blood culture bottles in routine clinical practice.
早期和适当的抗生素治疗可改善败血症患者的临床预后;因此,减少鉴定(ID)和抗菌药物敏感性测试(AST)结果的周转时间至关重要。我们建立了一种使用固体培养基对阳性血培养肉汤样本进行短期孵育来快速进行 ID 和 AST 的方法,并使用两种快速 ID 系统和一种快速 AST 方法评估了其相对于传统方法的性能。
共纳入 254 份单微生物样本。阳性血培养样本在血琼脂平板上孵育六小时,使用 MicroFlex LT(布鲁克·道尔顿)和 Vitek-MS(生物梅里埃)系统进行鉴定,然后使用 Vitek2 系统(生物梅里埃)进行 AST。
MicroFlex LT 和 Vitek-MS 平台的正确种属水平 ID 率分别为 82.3%(209/254)和 78.3%(199/254)。对于测试的 1,174 种微生物/抗菌药物组合,快速 AST 方法与传统方法的总符合率为 97.8%(1,148/1,174),非常大误差率为 0.5%,主要误差率为 0.7%,次要误差率为 1.0%。
常规实施这种短期孵育方法可以在血培养阳性检测当天提供 ID 结果,并比传统 AST 方法早一天。这种简单的方法将非常有助于在常规临床实践中快速鉴定和 AST 阳性血培养瓶中的细菌。