Servicio de Microbiología y Parasitología, Hospital Universitario La Paz, Paseo de la Castellana 261, 28046 Madrid, Spain.
J Infect. 2012 Dec;65(6):513-20. doi: 10.1016/j.jinf.2012.08.013. Epub 2012 Aug 30.
The objective of this study was to evaluate the reliability and accuracy of the combined use of MALDI-TOF MS bacterial identification and the Vitek-2 Compact antimicrobial susceptibility testing (AST) directly from positive blood cultures.
Direct identification by MALDI-TOF MS and AST were performed in parallel to the standard methods in all positively flagged blood cultures bottles during the study period.
Three hundred and twenty four monomicrobial positive blood cultures were included in the present study, with 257 Gram-negative and 67 Gram-positive isolates. MALDI-TOF MS identification directly from blood bottles reported the correct identification for Enterobacteriaceae in 97.7%, non-fermentative Gram-negative bacilli 75.0%, Staphylococcus aureus 75.8%, coagulase negative staphylococci 63.3% and enterococci 63.3%. A total 6156 isolate/antimicrobial agent combinations were tested. Enterobacteriaceae group and non-fermentative Gram-negative Bacilli showed an agreement of 96.67% and 92.30%, respectively, for the Gram-positive cocci the overall agreement found was 97.84%.
We conclude that direct identification by MALDI-TOF and inoculation of Vitek-2 Compact AST with positive blood culture bottles yielded very good results and decreased time between initial inoculation of blood culture media and determination of the antibiotic susceptibility for Gram-negative rods and Gram-positive cocci causing bacteremia.
本研究旨在评估 MALDI-TOF MS 细菌鉴定与 Vitek-2 Compact 抗菌药敏试验(AST)联合直接从阳性血培养物中应用的可靠性和准确性。
在研究期间,所有阳性 flagged 血培养瓶均同时平行进行 MALDI-TOF MS 直接鉴定和 AST。
本研究共纳入 324 例单一致病菌阳性血培养物,其中革兰氏阴性菌 257 株,革兰氏阳性菌 67 株。MALDI-TOF MS 直接从血瓶中鉴定报告肠杆菌科的正确鉴定率为 97.7%,非发酵革兰氏阴性杆菌为 75.0%,金黄色葡萄球菌为 75.8%,凝固酶阴性葡萄球菌为 63.3%,肠球菌为 63.3%。共测试了 6156 株分离物/抗菌药物组合。肠杆菌科和非发酵革兰氏阴性杆菌的一致性分别为 96.67%和 92.30%,而革兰氏阳性球菌的总一致性为 97.84%。
我们得出结论,MALDI-TOF 直接鉴定和接种 Vitek-2 Compact AST 从阳性血培养瓶中获得了非常好的结果,并缩短了革兰氏阴性杆菌和引起菌血症的革兰氏阳性球菌初始接种血培养介质与确定抗生素敏感性之间的时间。