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评估用于诊断人工膝关节感染的滑膜液属特异性和组特异性快速聚合酶链反应检测试剂盒

Evaluation of a Genus- and Group-Specific Rapid PCR Assay Panel on Synovial Fluid for Diagnosis of Prosthetic Knee Infection.

作者信息

Melendez Dante P, Greenwood-Quaintance Kerryl E, Berbari Elie F, Osmon Douglas R, Mandrekar Jayawant N, Hanssen Arlen D, Patel Robin

机构信息

Division of Infectious Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

J Clin Microbiol. 2016 Jan;54(1):120-6. doi: 10.1128/JCM.02302-15. Epub 2015 Nov 4.

Abstract

We evaluated a genus- and group-specific PCR assay panel using 284 prosthetic knee synovial fluid samples collected from patients presenting to our institution with implant failure. Using the Musculoskeletal Infection Society diagnostic criteria, 88 and 196 samples were classified as showing prosthetic joint infection (PJI) and aseptic failure (AF), respectively. Sensitivities of the synovial fluid PCR panel and culture were 55.6% and 76.1% (P ≤ 0.001), respectively, and specificities were 91.8% and 97.4% (P = 0.016), respectively. Among the 70 subjects who had received antibiotics within the month preceding synovial fluid aspiration (48 of whom had PJI), PCR panel and synovial fluid culture sensitivities were 64.5% and 85.4%, respectively (P < 0.0001). In this group, the PCR panel detected Staphylococcus aureus in two culture-negative PJI cases. Overall, the evaluated molecular diagnostic tool had low sensitivity when applied to synovial fluid.

摘要

我们使用从因植入物失败前来我院就诊的患者中收集的284份人工膝关节滑液样本,对一种属和组特异性聚合酶链反应(PCR)检测方法进行了评估。根据肌肉骨骼感染学会的诊断标准,分别有88份和196份样本被分类为显示人工关节感染(PJI)和无菌性失败(AF)。滑液PCR检测方法和培养的敏感性分别为55.6%和76.1%(P≤0.001),特异性分别为91.8%和97.4%(P = 0.016)。在滑液抽吸前一个月内接受过抗生素治疗的70名受试者中(其中48人患有PJI),PCR检测方法和滑液培养的敏感性分别为64.5%和85.4%(P < 0.0001)。在该组中,PCR检测方法在两例培养阴性的PJI病例中检测到了金黄色葡萄球菌。总体而言,所评估的分子诊断工具应用于滑液时敏感性较低。

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