P. L. Lewis, S. E. Graves, Australian Orthopaedic Association National Joint Replacement Registry (AOANJRR), Adelaide, South Australia, Australia P. L. Lewis, Wakefield Orthopaedic Clinic, Adelaide, South Australia, Australia A. Cuthbert, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, South Australia D. Parker, Sydney Orthopaedic Research Institute, Chatswood, New South Wales, Australia P. Myers, Brisbane Orthopaedic & Sports Medicine Centre, Spring Hill, Queensland, Australia.
Clin Orthop Relat Res. 2019 Jun;477(6):1402-1410. doi: 10.1097/CORR.0000000000000541.
Patellofemoral replacements (PFRs) have a higher rate of revision than unicompartmental knee arthroplasty or TKA. However, there is little information regarding why PFRs are revised, the components used for these revisions, or the outcome of the revision procedure. Some contend that PFR is a bridging procedure that can easily be revised to a TKA with similar results as a primary TKA; however, others dispute this suggestion.
QUESTIONS/PURPOSES: (1) In the setting of a large national registry, what were the reasons for revision of PFR to TKA and was the level of TKA constraint used in the revision associated with a subsequent risk of rerevision? (2) Is the risk of revision of the TKA used to revise a PFR greater than the risk of revision after a primary TKA and greater than the risk of rerevision after revision TKA?
Data were obtained from the Australian Orthopaedic Association Joint Replacement Registry through December 31, 2016, for TKA revision procedures after PFR. Because revisions for infection may be staged procedures resulting in further planned operations, for the revision analyses, these were excluded. There were 3251 PFRs, 482 of which were revised to TKA during the 17-year study period. The risk of second revision was calculated using Kaplan-Meier estimates of survivorship for PFRs revised to TKAs, and that risk was compared with the risk of first revision after TKA and also with the risk of a second revision after revision TKA. Hazard ratios (HRs) from Cox proportional hazards models were used to compare second revision rates among the different levels of prosthesis constraint used in the index revision after PFR (specifically, cruciate-retaining versus cruciate-substituting).
The main reasons for revising a PFR to TKA were progression of disease (56%), loosening (17%), and pain (12%). With the numbers available for analysis, there was no difference in the risk of a second revision when a PFR was revised to a cruciate-retaining TKA than when it was revised to a cruciate-substituting TKA (HR, 1.24 [0.65-2.36]; p = 0.512). A total of 204 (42%) of the PFR revisions had the patella component revised when the PFR was converted to a TKA. There difference in rates of second revision when the patella component was revised or not revised (HR, 1.01 [0.55-1.85]; p = 0.964). When we eliminated the devices that ceased to be used before 2005 (older devices), we found no change in the overall risk of repeat revision. The risk of a PFR that was revised to a TKA undergoing a second revision was greater than the risk of TKA undergoing a first revision (HR, 2.39 [1.77-3.24]; p < 0.001), but it was less than the risk of a revision TKA undergoing a second revision (HR, 0.60 [0.43-0.81]; p = 0.001).
The risk of second revision when a PFR is revised is not altered if cruciate-retaining or posterior-stabilized TKA is used for the revision nor if the patella component is revised or not revised. The risk of repeat revision after revision of a PFR to a TKA was much higher than the risk of revision after a primary TKA, and these findings did not change when we analyzed only devices in use since 2005. When PFR is used for the management of isolated patellofemoral osteoarthritis, patients should be counselled not only about the high revision rate of the primary procedure, but also the revision rate after TKA. Further studies regarding the functional outcomes of these procedures may help clarify the value of PFRs and subsequent revisions.
Level III, therapeutic study.
髌股关节置换术(PFR)的翻修率高于单髁膝关节置换术或全膝关节置换术。然而,关于为什么要翻修 PFR、用于这些翻修的组件以及翻修手术的结果的信息却很少。一些人认为 PFR 是一种过渡性手术,可以很容易地用与原发性 TKA 相似的结果翻修成 TKA;然而,其他人则对此表示质疑。
问题/目的:(1)在大型国家注册中心的背景下,翻修 PFR 为 TKA 的原因是什么,以及在翻修中使用的 TKA 约束级别是否与随后的再翻修风险相关?(2)翻修 PFR 所使用的 TKA 的翻修风险是否大于原发性 TKA 的翻修风险,以及大于翻修 TKA 的再翻修风险?
数据来自澳大利亚矫形协会关节置换登记处,截至 2016 年 12 月 31 日,用于 PFR 翻修后的 TKA 翻修程序。由于感染的翻修可能是分期手术,导致进一步计划手术,因此在翻修分析中,这些病例被排除在外。共有 3251 例 PFR,其中 482 例在 17 年的研究期间翻修为 TKA。使用 PFR 翻修为 TKA 的生存概率的 Kaplan-Meier 估计来计算第二次翻修的风险,并将该风险与 TKA 翻修后的第一次翻修风险进行比较,也与翻修 TKA 后的第二次翻修风险进行比较。使用 Cox 比例风险模型的风险比(HR)比较了在 PFR 索引翻修中使用的不同水平的假体约束(具体为保留交叉韧带的与替代交叉韧带的)之间的第二次翻修率。
将 PFR 翻修为 TKA 的主要原因是疾病进展(56%)、松动(17%)和疼痛(12%)。根据可分析的数字,当 PFR 翻修为保留交叉韧带的 TKA 时,与翻修为替代交叉韧带的 TKA 相比,第二次翻修的风险没有差异(HR,1.24[0.65-2.36];p=0.512)。在 PFR 转换为 TKA 时,共有 204 例(42%)的 PFR 翻修翻修了髌骨组件。当髌骨组件被翻修或未被翻修时,第二次翻修的比率没有差异(HR,1.01[0.55-1.85];p=0.964)。当我们消除了在 2005 年之前停止使用的器械(旧器械)时,我们没有发现总体重复翻修风险的变化。翻修为 TKA 的 PFR 再次接受翻修的风险大于初次接受 TKA 翻修的风险(HR,2.39[1.77-3.24];p<0.001),但小于翻修 TKA 再次接受翻修的风险(HR,0.60[0.43-0.81];p=0.001)。
如果使用保留交叉韧带的或后稳定的 TKA 进行翻修,或者翻修或不翻修髌骨组件,翻修 PFR 后第二次翻修的风险不会改变。翻修 PFR 为 TKA 后的再次翻修风险远高于初次 TKA 翻修后的风险,当我们只分析自 2005 年以来使用的器械时,这些发现没有改变。当 PFR 用于治疗孤立性髌股关节炎时,不仅要告知患者初次手术的高翻修率,还要告知他们 TKA 翻修后的翻修率。关于这些手术的功能结果的进一步研究可能有助于澄清 PFR 和随后的翻修的价值。
三级,治疗性研究。