Rothman Orthopaedic Institute at Thomas Jefferson University, Philadelphia, PA; Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv, Israel.
Rothman Orthopaedic Institute at Thomas Jefferson University, Philadelphia, PA.
J Arthroplasty. 2019 Nov;34(11):2730-2736.e1. doi: 10.1016/j.arth.2019.06.016. Epub 2019 Jun 13.
The guidelines for diagnosis of periprosthetic joint infection (PJI) introduced by the American Academy of Orthopaedic Surgeons served the orthopedic community well. However, they have never been validated and do not account for newer diagnostic modalities. Our aim was to update current guidelines and develop an evidence-based and validated diagnostic algorithm.
This multi-institutional study examined total joint arthroplasty patients from 3 institutions. Patients fulfilling major criteria for infection as defined by Musculoskeletal Infection Society were considered infected (n = 684). Patients undergoing aseptic revision for a noninfective indication and did not show evidence of PJI or undergo reoperation within 2 years served as a noninfected control group (n = 820). The algorithm was validated on a separate cohort of 422 cases.
The first step in evaluating PJI should include a physical examination, followed by serum C-reactive protein, erythrocyte sedimentation rate, and D-dimer. If at least one of these tests are elevated, or if high clinical suspicion exists, joint aspiration should be performed, sending the fluid for a white blood cell count, leukocyte esterase, polymorphonuclear percentage, and culture. Alpha defensin did not show added benefit as a routine diagnostic test. In inconclusive cases, intraoperative findings including gross purulence, histology, and next-generation sequencing or a single positive culture can aid in making the diagnosis. The proposed algorithm demonstrated a high sensitivity (96.9%) and specificity (99.5%).
This validated, evidence-based algorithm for diagnosing PJI should guide clinicians in the workup of patients undergoing revision arthroplasty and improve clinical practice. It also has the potential to reduce cost.
美国矫形外科医师学会(AAOS)发布的假体周围关节感染(PJI)诊断指南很好地服务了矫形外科医生群体。然而,它们从未经过验证,也没有考虑到更新的诊断方法。我们的目的是更新当前的指南,并制定一个基于证据和经过验证的诊断算法。
这项多机构研究检查了来自 3 家机构的全关节置换患者。符合骨髓炎协会定义的感染主要标准的患者被认为是感染(n=684)。因非感染性原因进行无菌翻修且无 PJI 证据或在 2 年内再次手术的患者作为未感染对照组(n=820)。该算法在另一个 422 例病例队列中进行了验证。
评估 PJI 的第一步应包括体格检查,然后是血清 C 反应蛋白、红细胞沉降率和 D-二聚体。如果至少有一项检查升高,或者临床高度怀疑存在感染,应进行关节抽吸术,并将抽出液送检白细胞计数、白细胞酯酶、多形核细胞百分比和培养。α-防御素作为常规诊断测试没有显示出额外的益处。在结果不确定的情况下,术中发现包括大量脓性分泌物、组织学、下一代测序或单个阳性培养物有助于做出诊断。所提出的算法具有高敏感性(96.9%)和特异性(99.5%)。
这种经过验证的、基于证据的 PJI 诊断算法应指导临床医生对接受翻修关节置换术的患者进行评估,并改善临床实践。它还有降低成本的潜力。