Department of Orthopaedic Surgery, Harbor-UCLA Medical Center, Torrance, California.
Department of Orthopaedic Surgery, David Geffen School of Medicine at UCLA, Los Angeles, California.
J Bone Joint Surg Am. 2019 Feb 6;101(3):257-264. doi: 10.2106/JBJS.18.00134.
The utilization of lymphocyte transformation testing (LTT) has increased for diagnosing metal sensitivity associated with total knee arthroplasty (TKA), but its validity for the diagnosis of TKA failure due to an immune reaction has not been established. In this study, we sought to characterize the relationship of a positive LTT result to histopathologic findings and clinical and functional outcomes.
This was a retrospective study of 27 well-fixed, aseptic, primary TKA cases in which the patient had persistent pain and/or stiffness and underwent revision due to a suspected metal allergy to nickel, as determined on the basis of positive LTT. Revision procedures were performed by a single experienced arthroplasty surgeon. Periprosthetic tissue samples obtained at the time of revision surgery were scored using the aseptic lymphocyte-dominated vasculitis-associated lesion (ALVAL) scoring system.
Eight patients were categorized as mildly reactive; 8 patients, moderately reactive; and 11 patients, highly reactive to nickel by LTT. The predominant findings on routine histopathologic analysis were fibrosis and varying degrees of lymphocytic infiltration in 17 (63%) of the 27 cases. The average ALVAL score of the cohort was 3.1 ± 1.9, of a maximum score of 10. Average Knee Society Score (KSS) values improved post-revision, as did range of motion (all p < 0.01). Neither LTT stimulation index as a continuous variable nor as a categorical variable (mildly reactive, moderately reactive, highly reactive) was correlated with ALVAL score, pre-revision function (as assessed by KSS-clinical, KSS-functional, and range of motion), or change in function at the most recent follow-up (0.015 < r < 0.30, 0.13 < p < 0.95). In addition, the ALVAL score did not correlate significantly with either pre-revision or post-revision KSS or range of motion (0.061 < r < 0.365, 0.09 < p < 0.88).
On the basis of this analysis, including histopathologic assessment, LTT results alone were insufficient for the diagnosis of TKA failure due to an immune reaction. A positive LTT may not indicate that an immune reaction is the cause of pain and stiffness post-TKA. The role of LTT in assessing TKA failure from an immune reaction needs further investigation. Diagnostic criteria for such TKA failure need to be established.
Diagnostic Level IV. See Instructions for Authors for a complete description of levels of evidence.
淋巴细胞转化试验(LTT)的应用增加了对与全膝关节置换术(TKA)相关的金属敏感性的诊断,但它在诊断由于免疫反应引起的 TKA 失败方面的有效性尚未得到证实。在这项研究中,我们试图描述阳性 LTT 结果与组织病理学发现以及临床和功能结果之间的关系。
这是一项回顾性研究,共纳入 27 例固定良好、无菌的原发性 TKA 患者,这些患者因疑似镍金属过敏而出现持续性疼痛和/或僵硬,并进行了翻修,这是基于 LTT 阳性结果确定的。翻修手术由一位经验丰富的关节置换外科医生进行。在翻修手术时获得的假体周围组织样本使用无菌性淋巴细胞为主的血管炎相关病变(ALVAL)评分系统进行评分。
8 例患者被归类为轻度反应;8 例患者为中度反应;11 例患者对镍的 LTT 反应高度阳性。27 例患者中有 17 例(63%)常规组织病理学分析的主要发现为纤维化和不同程度的淋巴细胞浸润。该队列的平均 ALVAL 评分为 3.1±1.9,最高评分为 10 分。翻修后平均膝关节协会评分(KSS)值提高,活动范围也增加(均 p<0.01)。无论是 LTT 刺激指数作为连续变量还是作为分类变量(轻度反应、中度反应、高度反应),均与 ALVAL 评分、翻修前功能(由 KSS-临床、KSS-功能和活动范围评估)或最近随访时的功能变化无关(0.015<r<0.30,0.13<p<0.95)。此外,ALVAL 评分与翻修前或翻修后的 KSS 或活动范围无显著相关性(0.061<r<0.365,0.09<p<0.88)。
根据本分析,包括组织病理学评估,单独的 LTT 结果不足以诊断由于免疫反应引起的 TKA 失败。阳性 LTT 并不能表明免疫反应是 TKA 后疼痛和僵硬的原因。LTT 在评估免疫反应引起的 TKA 失败中的作用需要进一步研究。需要建立此类 TKA 失败的诊断标准。
诊断 IV 级。有关证据水平的完整描述,请参见作者说明。