Division of Public Health, Infectious Diseases, and Occupational Medicine, Department of Medicine, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.
Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.
J Clin Microbiol. 2022 Dec 21;60(12):e0112622. doi: 10.1128/jcm.01126-22. Epub 2022 Nov 21.
The diagnosis of periprosthetic joint infection (PJI) is challenging, often requiring multiple clinical specimens and diagnostic techniques, some with prolonged result turnaround times. Here, the diagnostic performance of the Investigational Use Only (IUO) BioFire Joint Infection (JI) Panel was compared to 16S rRNA gene-based targeted metagenomic sequencing (tMGS) applied to synovial fluid for PJI diagnosis. Sixty synovial fluid samples from knee arthroplasty failure archived at -80°C were tested. Infectious Diseases Society of America (IDSA) diagnostic criteria were used to classify PJI. For culture-positive PJI with pathogens targeted by the JI panel, JI panel sensitivity was 91% (21/23; 95% confidence interval [CI], 73 to 98%), and tMGS sensitivity was 96% (23/24; 95% CI, 80 to 99%) ( = 0.56). Overall sensitivities of the JI panel and tMGS for PJI diagnosis were 56% (24/43; 95% CI, 41 to 70%) and 93% (41/44; 95% CI, 82 to 98%), respectively ( < 0.001). JI panel and tMGS overall specificities were 100% (16/16; 95% CI, 81 to 100%) and 94% (15/16; 95% CI, 72 to 99%), respectively. While the clinical sensitivity of the JI panel was excellent for on-panel microorganisms, overall sensitivity for PJI diagnosis was low due to the absence of Staphylococcus epidermidis, a common causative pathogen of PJI, on the panel. A PJI diagnostic algorithm for the use of both molecular tests is proposed.
假体周围关节感染(PJI)的诊断具有挑战性,通常需要多个临床标本和诊断技术,其中一些需要较长的检测周转时间。在此,比较了仅限研究使用(IUO)的 BioFire 关节感染(JI)面板与针对滑液的基于 16S rRNA 基因的靶向宏基因组测序(tMGS)在 PJI 诊断中的诊断性能。测试了 60 份保存在-80°C 的膝关节置换失败的关节滑液存档样本。使用感染病学会(IDSA)诊断标准对 PJI 进行分类。对于 JI 面板靶向病原体的培养阳性 PJI,JI 面板的敏感性为 91%(21/23;95%置信区间 [CI],73 至 98%),tMGS 敏感性为 96%(23/24;95%CI,80 至 99%)(=0.56)。JI 面板和 tMGS 用于 PJI 诊断的总体敏感性分别为 56%(24/43;95%CI,41 至 70%)和 93%(41/44;95%CI,82 至 98%)(<0.001)。JI 面板和 tMGS 的总体特异性分别为 100%(16/16;95%CI,81 至 100%)和 94%(15/16;95%CI,72 至 99%)。虽然 JI 面板针对面板上的微生物具有出色的临床敏感性,但由于面板上缺少表皮葡萄球菌(一种常见的 PJI 病原体),因此整体 PJI 诊断敏感性较低。提出了一种用于两种分子检测的 PJI 诊断算法。