Department of Orthopaedic Surgery and Traumatology, Odense University Hospital; Department of Clinical Research, University of Southern Denmark, Odense.
Department of Regional Health Research, University of Southern Denmark, Odense; Department of Orthopaedic Surgery, Naestved Hospital. Naestved.
Acta Orthop. 2022 Jan 3;93:103-110. doi: 10.1080/17453674.2021.1999069.
Background and purpose - Patients having a knee arthroplasty revision for the indication "pain without loosening" may have a higher risk of re-revisions than patients revised for other indications. The primary aim of this study was to compare the survival of knee arthroplasties revised for "pain without loosening" compared with "aseptic loosening." The second was to investigate the prosthesis survival rates in 3 surgical subgroups (total knee arthroplasty (TKA)-TKA; partial revision (revision of tibial or femoral component); unicompartmental knee arthroplasty-TKA) and to compare the prosthesis survival rates for 1997-2009 and 2010-2018. Patients and methods - 4,299 revisions were identified in the period 1997-2018 from the Danish Knee Arthroplasty Register. Of these, 1,111 (26%) were performed due to "pain without loosening" without any other indications, 674 (16%) due to "pain without loosening" combined with other indications, and 2,514 (59%) due to "aseptic loosening". Survival analysis was performed by a Cox multivariate analysis and Kaplan-Meier curves were presented. Results - The cumulated proportions of re-revision after 2, 5, and 20 years were 12% (95% CI 10-14), 18% (CI 16-20), and 23% (CI 20-25) for "pain without loosening" versus 11% (CI 9.3-12), 16% (CI 14-17), and 19% (CI 18-21) for "aseptic loosening." There were no statistically significant differences between the 2 indications in repeated analyses for each of the surgical subgroups. The hazard ratio for re-revision comparing "pain without loosening" with "aseptic loosening" was 1.03 (CI 0.87-1.2). The 8-year risk of re-revision for "pain without loosening" was 22% (CI 19-26) versus 22% (CI 20-25) for "aseptic loosening" in the period from 1997-2009, and 18% (CI 15-22) versus 14% (CI 13-16) in the period from 2010-2018. Interpretation - The risk of re-revision was similar for patients having a knee arthroplasty revision for the indication "pain without loosening" compared with "aseptic loosening." However, we observed a slight improvement of prosthesis survival rates after revisions for both indications from 1997-2009 to 2010-2018. We cannot recommend for or against revision in cases with "pain without loosening" based on these data alone.
背景与目的 - 因“无松动性疼痛”而行膝关节翻修术的患者,其再次翻修的风险可能高于因其他指征而行翻修术的患者。本研究的主要目的是比较因“无松动性疼痛”与“无菌性松动”而行膝关节翻修术的患者的生存率。第二个目的是调查在 3 个手术亚组(全膝关节置换术(TKA)-TKA;部分翻修术(胫骨或股骨部件的翻修);单髁膝关节置换术-TKA)中的假体生存率,并比较 1997-2009 年和 2010-2018 年的假体生存率。
患者和方法 - 1997-2018 年期间,从丹麦膝关节置换登记处确定了 4299 例翻修手术。其中,1111 例(26%)因“无松动性疼痛”而无其他任何指征,674 例(16%)因“无松动性疼痛”合并其他指征,2514 例(59%)因“无菌性松动”。通过 Cox 多变量分析进行生存分析,并呈现 Kaplan-Meier 曲线。
结果 - 2、5 和 20 年后再次翻修的累积比例分别为 12%(95%CI 10-14)、18%(CI 16-20)和 23%(CI 20-25)的“无松动性疼痛”,11%(CI 9.3-12)、16%(CI 14-17)和 19%(CI 18-21)的“无菌性松动”。在对每个手术亚组的重复分析中,这两个指征之间没有统计学上的显著差异。与“无菌性松动”相比,“无松动性疼痛”再次翻修的风险比为 1.03(CI 0.87-1.2)。在 1997-2009 年期间,“无松动性疼痛”的 8 年再次翻修风险为 22%(CI 19-26),与“无菌性松动”的 22%(CI 20-25)相当,在 2010-2018 年期间,这一风险为 18%(CI 15-22),与“无菌性松动”的 14%(CI 13-16)相当。
结论 - 因“无松动性疼痛”而行膝关节翻修术的患者与因“无菌性松动”而行膝关节翻修术的患者再次翻修的风险相似。然而,我们观察到,从 1997-2009 年到 2010-2018 年,这两个指征的假体生存率都略有提高。我们不能仅凭这些数据建议或反对因“无松动性疼痛”而行翻修手术。