Department of Orthopaedic Surgery, New England Baptist Hospital, Boston, Massachusetts.
Department of Research, New England Baptist Hospital, Boston, Massachusetts.
J Arthroplasty. 2018 Jul;33(7S):S100-S104. doi: 10.1016/j.arth.2018.03.010. Epub 2018 Mar 15.
There has been a recent interest in custom-made partial knee arthroplasties to provide patient-specific instrumentation and better fit of the prosthesis. While unicondylar knee arthroplasties (UKAs) have demonstrated good outcomes and durable results in many studies, there is little evidence on outcomes of these custom-made implants.
We performed a retrospective review of all custom-made UKAs performed at our institution by one surgeon from 2008 to 2015. We analyzed preoperative demographics, clinical follow-up evaluations, and radiographs and performed an analysis of risk factors including age, gender, height, weight, body mass index, and tibial insert thickness. The incidence of revision surgery, radiographic failures indicating component loosening, and symptomatic clinically failed implants was calculated at an average of 54.0 months of follow-up.
We analyzed 115 consecutive custom-made medial UKAs from a single surgeon at our institution and found 29 (25.2%) UKAs had failed at an average of 33.1 months after surgery. Reasons for failure included aseptic femoral loosening (10), aseptic tibial loosening (8), loosening of both components (4), infection (3), progression of osteoarthritis (2), pain (1), and dislodged polyethylene insert (1). We found a significant relationship between implant failure and body mass index; no other study variables were statistically significant.
We found a relatively high rate of aseptic loosening and particularly femoral component loosening in the short- to intermediate-term follow-up period. While further study of larger numbers of custom-made UKA from multiple institutions may help verify these findings, we recommend careful consideration of the use of this implant.
最近人们对定制的部分膝关节置换术产生了兴趣,以提供患者特定的器械和更好的假体适配。虽然单髁膝关节置换术(UKA)在许多研究中已经证明了良好的效果和持久的结果,但对于这些定制植入物的结果证据很少。
我们对 2008 年至 2015 年期间由一位外科医生在我们机构进行的所有定制 UKA 进行了回顾性研究。我们分析了术前人口统计学、临床随访评估和影像学,并对包括年龄、性别、身高、体重、体重指数和胫骨插入物厚度在内的风险因素进行了分析。在平均 54.0 个月的随访中,计算了翻修手术、影像学失败表明组件松动以及有症状的临床失败植入物的发生率。
我们分析了来自我们机构的一位外科医生的 115 例连续定制内侧 UKA,发现 29 例(25.2%)UKA 在手术后平均 33.1 个月时失败。失败的原因包括无菌性股骨松动(10 例)、无菌性胫骨松动(8 例)、两个组件松动(4 例)、感染(3 例)、骨关节炎进展(2 例)、疼痛(1 例)和聚乙烯插入物移位(1 例)。我们发现,假体失败与体重指数之间存在显著关系;其他研究变量没有统计学意义。
我们发现,在短期至中期随访期间,无菌性松动,特别是股骨组件松动的发生率相对较高。虽然进一步研究来自多个机构的更多数量的定制 UKA 可能有助于验证这些发现,但我们建议谨慎考虑使用这种植入物。