Banke I J, Stade N, Prodinger P M, Mühlhofer H M, Thomas P, Thomas B, Summer B, van Griensven M, von Eisenhart-Rothe R, Gollwitzer H
Klinik und Poliklinik für Orthopädie und Sportorthopädie, Klinikum rechts der Isar der TU München, Ismaninger Str. 22, 81675, München, Deutschland.
Klinik und Poliklinik für Dermatologie und Allergologie der LMU München, Frauenlobstraße 9-11, 80337, München, Deutschland.
Orthopade. 2015 Dec;44(12):93, 936-8, 940-1. doi: 10.1007/s00132-015-3188-7.
The diagnosis and treatment of periprosthetic joint infection (PJI) remain true clinical challenges. PJI diminishes therapeutic success, causes dissatisfaction for the patient and medical staff, and often requires extensive surgical revision(s). At the present time, an extensive multimodal algorithmic approach is used to avoid time- and cost-consuming diagnostic aberrations. However, especially in the case of the frequent and clinically most relevant "low-grade" PJI, the current diagnostic "gold standard" has reached its limits.
Synovial biomarkers are thought to close this diagnostic gap, hopefully enabling the safe differentiation among aseptic, (chronic) septic, implant allergy-related and the arthrofibrotic genesis of symptomatic arthroplasty. Therefore, joint aspiration for obtaining synovial fluid is preferred over surgical synovial tissue biopsy because of the faster results, greater practicability, greater patient safety, and lower costs. In addition to the parameters synovial IL-6, CRP, and leukocyte esterase, novel biomarkers such as antimicrobial peptides and other proinflammatory cytokines are currently highlighted because of their very high to excellent diagnostic accuracy.
Independent multicenter validation studies are required to show whether a set of different innovative synovial fluid biomarkers rather than a few single parameters is favorable for a safe "one-stop shop" differential diagnosis of PJI.
人工关节周围感染(PJI)的诊断和治疗仍然是真正的临床挑战。PJI降低了治疗成功率,导致患者和医护人员不满,并且常常需要进行广泛的手术翻修。目前,采用广泛的多模式算法方法来避免耗时和成本高昂的诊断偏差。然而,特别是在频繁且临床上最相关的“低度”PJI病例中,当前的诊断“金标准”已达到其极限。
滑膜生物标志物被认为可以弥补这一诊断差距,有望实现对无菌性、(慢性)感染性、植入物过敏相关以及症状性关节成形术的关节纤维性变病因进行安全鉴别。因此,由于结果更快、实用性更强、患者安全性更高且成本更低,抽取关节液获取滑液优于手术滑膜组织活检。除了滑膜白细胞介素-6、CRP和白细胞酯酶等参数外,抗菌肽和其他促炎细胞因子等新型生物标志物目前因其极高至优异的诊断准确性而受到关注。
需要进行独立的多中心验证研究,以表明一组不同的创新滑液生物标志物而非少数几个单一参数是否有利于对PJI进行安全的“一站式”鉴别诊断。