Kobayashi Naomi, Inaba Yutaka, Choe Hyonmin, Iwamoto Naoyuki, Ishida Takashi, Yukizawa Yohei, Aoki Chie, Ike Hiroyuki, Saito Tomoyuki
Department of Orthopaedic Surgery, Yokohama City University, Japan.
Diagn Microbiol Infect Dis. 2009 Jun;64(2):172-6. doi: 10.1016/j.diagmicrobio.2009.01.033. Epub 2009 Apr 2.
The aim of this study was to validate the accuracy, sensitivity, and specificity of a methicillin-resistant Staphylococcus (MRS) real-time polymerase chain reaction (PCR) assay in clinical periprosthetic infection cases. A total of 36 cases of revision arthroplasty were enrolled in this prospective study, and the primer and probe set of a methicillin-resistant Staphylococcus aureus detection kit were used for the specific detection of the MecA gene with a LightCycler system. The specimens were also tested in microbiologic cultures and histopathologic evaluations. Of the 36 cases tested, 14 were found to be PCR positive for MRS infection. Of these 14 cases, however, only 8 were also found to be MRS infected using the culture method, whereas 3 were culture negative and 3 samples showed growth of another organism. The accuracy, sensitivity, and specificity were 0.83, 1.00, and 0.79, respectively. We conclude that the use of this approach will improve the diagnosis of MRS having a direct impact in the management of cases of periprosthetic infections.
本研究的目的是验证耐甲氧西林葡萄球菌(MRS)实时聚合酶链反应(PCR)检测方法在临床假体周围感染病例中的准确性、敏感性和特异性。本前瞻性研究共纳入36例翻修关节成形术病例,使用耐甲氧西林金黄色葡萄球菌检测试剂盒的引物和探针组,通过LightCycler系统对MecA基因进行特异性检测。标本还进行了微生物培养和组织病理学评估。在检测的36例病例中,14例MRS感染的PCR检测呈阳性。然而,在这14例病例中,使用培养方法仅发现8例也为MRS感染阳性,3例培养阴性,3份样本显示有其他微生物生长。准确性、敏感性和特异性分别为0.83、1.00和0.79。我们得出结论,使用这种方法将改善MRS的诊断,对假体周围感染病例的管理有直接影响。