E. Beit Ner, Department of Orthopedic Surgery, Yitzhak Shamir Medical Center, Zerifin, Israel, affiliated with the Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
E. Beit Ner, L. C. Biant, Manchester Orthopaedic Centre, Manchester University National Health Service Foundation Trust, Manchester, UK.
Clin Orthop Relat Res. 2021 Jun 1;479(6):1237-1249. doi: 10.1097/CORR.0000000000001651.
Failure to accurately replicate the native anatomy and biomechanics of the knee has been suggested to contribute to dissatisfaction after TKA. Custom implants promise a personalized surgical approach, with the aim of improving patient satisfaction and pain as well as lowering revision rates. However, some published research on custom TKA implants has found no clinically important improvements in postoperative validated outcomes scores, risks of revision or reoperation, and implant alignment. In the interest of helping to settle this controversy, a systematic review seems warranted.
QUESTION/PURPOSE: In this systematic review, we asked whether custom implants result in clinically important improvements over conventional off-the-shelf implants for anatomically uncomplicated primary TKA in terms of (1) validated outcomes scores, (2) the risk of revision or reoperation, and (3) implant alignment.
The US National Library of Medicine (PubMed/Medline), Embase, Web of Science, and Cochrane Database of Systematic Reviews were systematically searched to identify publications from the past 10 years relevant to this review. Publications that compared the clinical outcome measures, number of revisions and reoperations, and radiological assessment of implant alignment of custom and standard implants with validated endpoints were eligible for inclusion. In the interest of capturing as much potentially relevant information as possible, we applied no requirement for minimum follow-up duration. Clinical outcomes were assessed using patient-reported outcome (PROM) scores including the Knee Society Score (KSS), Forgotten Joint Score, and Knee Injury and Osteoarthritis Outcome Score. The risk for revision or reoperation were evaluated by the number of early and late manipulations, debridement procedures, and replacement of one or more components. Implant alignment was compared using postoperative deviation from the neutral (0°) mechanical axis of the limb and each component and the posterior tibial slope. All qualified studies were retrospective, and all compared custom implants with standard implants. Data on 1510 patients were reviewed (749 with custom implants and 761 with off-the-shelf implants). The mean follow-up time ranged from 12 to 33 months.
There was no apparent advantage to custom implants in terms of PROM scores. Of the five studies evaluating clinical outcomes, only one reported better KSS-Function scores at 3 months; two reported no difference, and two found inferior KSS scores. In several studies, custom implants were associated with more frequent reoperations than standard implants. Although in general there were no differences between custom and standard implants in terms of mean coronal plane limb alignment, one of seven studies found that the proportion of patients whose alignment was outside ± 3° from the neutral axis in the coronal plane was lower in the custom group than in the standard group.
With generally poorer outcomes scores for pain and function, generally higher risks of reoperation and reintervention, and no overall benefit to alignment, custom implants for primary TKA for the general population currently appear to be inferior to standard implants. Whether the slight reduction in the proportion of patients with alignment outliers observed in a minority of studies will result in a substantial reduction in revision risk over time must be addressed by future studies. However, until or unless such a reduction is proven, we recommend against the routine use of custom implants in practice because of increased costs and the risks associated with their novelty.
Level III, therapeutic study.
有人认为,未能准确复制膝关节的原生解剖结构和生物力学特性是导致全膝关节置换术(TKA)后患者不满意的原因之一。定制植入物承诺采用个性化的手术方法,旨在提高患者满意度和减轻疼痛,同时降低翻修率。然而,一些关于定制 TKA 植入物的已发表研究发现,术后经过验证的结果评分、翻修或再次手术的风险以及植入物的对准方面并没有临床意义上的显著改善。为了解决这一争议,似乎有必要进行系统评价。
问题/目的:在这项系统评价中,我们询问了在解剖结构不复杂的原发性 TKA 中,定制植入物是否比传统的现成植入物在以下方面具有临床意义上的改善:(1)经过验证的结果评分;(2)翻修或再次手术的风险;(3)植入物的对准。
美国国家医学图书馆(PubMed/Medline)、Embase、Web of Science 和 Cochrane 系统评价数据库被系统地搜索,以确定与本次评价相关的过去 10 年的出版物。有资格纳入的出版物比较了定制和标准植入物的临床结果测量、翻修和再次手术的数量以及植入物对准的放射学评估,这些评估均采用经过验证的终点。为了尽可能多地获取潜在相关信息,我们没有要求最低随访时间。临床结果使用患者报告的结果(PROM)评分进行评估,包括膝关节协会评分(KSS)、遗忘关节评分和膝关节损伤和骨关节炎结果评分。通过早期和晚期操作、清创术以及一个或多个组件的更换数量来评估翻修或再次手术的风险。使用术后肢体和每个组件的机械轴与中立(0°)轴的偏差以及后胫骨斜率来比较植入物的对准情况。所有合格的研究均为回顾性研究,均比较了定制植入物与标准植入物。共回顾了 1510 名患者的数据(749 名接受定制植入物,761 名接受现成植入物)。平均随访时间从 12 个月到 33 个月不等。
在 PROM 评分方面,定制植入物似乎没有明显优势。在评估临床结果的五项研究中,只有一项研究在 3 个月时报告了更好的 KSS-功能评分;两项研究没有差异,两项研究发现 KSS 评分较低。在几项研究中,定制植入物与标准植入物相比,更频繁地需要再次手术。尽管在冠状面肢体对准方面,定制和标准植入物的平均差异通常没有统计学意义,但有一项研究发现,定制组中冠状面偏离中立轴±3°的患者比例低于标准组。
由于疼痛和功能的结果评分较差,再次手术和干预的风险较高,并且对准方面没有整体获益,目前对于普通人群的原发性 TKA,定制植入物似乎不如标准植入物。在未来的研究中,必须解决少数研究中观察到的对准异常患者比例降低是否会导致翻修风险随着时间的推移而实质性降低的问题。然而,除非这种降低得到证实,否则我们不建议在实践中常规使用定制植入物,因为其成本增加且具有新颖性相关的风险。
III 级,治疗性研究。