Kobayashi Naomi, Inaba Yutaka, Choe Hyonmin, Aoki Chie, Ike Hiroyuki, Ishida Takashi, Iwamoto Naoyuki, Yukizawa Yohei, Saito Tomoyuki
Department of Orthopaedic Surgery, Yokohama City University, Yokohama, Japan.
J Bone Joint Surg Am. 2009 Dec;91(12):2896-902. doi: 10.2106/JBJS.I.00119.
Periprosthetic infection is one of the most serious complications of arthroplasty, and low-grade infections are particularly difficult to diagnose with use of conventional culture methods. Real-time polymerase chain reaction is a potentially viable way to overcome this detection problem as it is a more rapid and sensitive technique. In the current study, we used intraoperative polymerase chain reaction identification combined with a simple DNA-release method with ultrasonication to diagnose periprosthetic infections during revision surgery.
Thirty revision arthroplasty procedures were included in this prospective study. Surgical specimens were obtained intraoperatively, treated with ultrasonication, and then analyzed with real-time polymerase chain reaction. Methicillin-resistant Staphylococcus-specific polymerase chain reaction and 16S rRNA gene universal polymerase chain reaction were performed simultaneously to facilitate both specific and broad-range detection. Specimens obtained from the same sites were also analyzed with microbiologic culture and histopathological evaluation.
The specific polymerase chain reaction revealed methicillin-resistant Staphylococcus infection in specimens from six of the thirty operations analyzed in the present study, and the 16S rRNA gene universal polymerase chain reaction analysis was positive for specimens from thirteen operations. Conventional cultures revealed six methicillin-resistant Staphylococcus infections, two Staphylococcus aureus infections, one infection with another Staphylococcus species, and two Streptococcus infections. The sensitivity of the polymerase chain reaction method was 0.87 and the specificity was 0.8 when compared with the combined results of microbiologic culture and histopathological evaluation.
The ultrasonication method that we developed for accelerated DNA sample preparation as a replacement for conventional extraction made possible the potential intraoperative identification of periprosthetic infection during revision surgery. The simultaneous detection of methicillin-resistant Staphylococcus and broad-range bacterial infections would be invaluable for the informed selection of antibiotics and also for the formulation of the subsequent treatment strategy (a one-stage or two-stage revision) for the patient.
假体周围感染是关节置换术最严重的并发症之一,而低度感染尤其难以通过传统培养方法进行诊断。实时聚合酶链反应是克服这一检测难题的一种潜在可行方法,因为它是一种更快速且灵敏的技术。在本研究中,我们在翻修手术期间采用术中聚合酶链反应鉴定,并结合一种简单的超声DNA释放方法来诊断假体周围感染。
本前瞻性研究纳入了30例翻修关节置换手术。术中获取手术标本,经超声处理,然后进行实时聚合酶链反应分析。同时进行耐甲氧西林金黄色葡萄球菌特异性聚合酶链反应和16S rRNA基因通用聚合酶链反应,以实现特异性和广泛范围的检测。从相同部位获取的标本也进行微生物培养和组织病理学评估。
特异性聚合酶链反应显示,在本研究分析的30例手术中的6例标本中存在耐甲氧西林金黄色葡萄球菌感染,16S rRNA基因通用聚合酶链反应分析显示13例手术的标本呈阳性。传统培养显示6例耐甲氧西林金黄色葡萄球菌感染、2例金黄色葡萄球菌感染、1例其他葡萄球菌属感染和2例链球菌感染。与微生物培养和组织病理学评估的联合结果相比,聚合酶链反应方法的敏感性为0.87,特异性为0.8。
我们开发的用于加速DNA样本制备以替代传统提取方法的超声处理方法,使得在翻修手术期间对假体周围感染进行潜在的术中鉴定成为可能。同时检测耐甲氧西林金黄色葡萄球菌和广泛的细菌感染对于明智地选择抗生素以及为患者制定后续治疗策略(一期或二期翻修)将具有重要价值。