Department of Orthopaedic Surgery, Seoul National University Hospital, 101 Daehak-ro, Jongno-gu, Seoul, 110-744, Korea.
Knee Surg Sports Traumatol Arthrosc. 2013 Mar;21(3):620-8. doi: 10.1007/s00167-012-1998-2. Epub 2012 Apr 8.
The aims of this retrospective study were to provide the basis for the choice of prosthesis in revision total knee arthroplasty (TKA) and to evaluate the outcome with varus-valgus constrained prosthesis compared with posterior stabilized (PS) prosthesis.
One hundred and five patients (121 knees) received revision TKA; of which thirty-seven patients (42 knees) received PS prosthesis and sixty-eight patients (79 knees) received varus-valgus constrained prosthesis. The mean follow-up duration was 64.8 ± 31.5 months and 63.2 ± 28.1 months in the PS and varus-valgus constrained groups, respectively. The criterion of prosthesis choice was a subjective laxity assessed by the surgeon intraoperatively. A multivariate analysis was performed to evaluate the preoperative factors in the choice of the prosthesis.
The grade of femoral bone defect was the only factor that affected the choice of prosthesis. Clinical results improved significantly in both groups after surgery. There were no significant differences in clinical results between the two groups. Complication rates were 9.5 % in the PS group and 10.1 % in the varus-valgus constrained group, and the Kaplan-Meier survivorship analysis revealed 8-year component survival rates of 83.1 and 93.0 % in the PS and varus-valgus constrained groups, respectively.
Femoral bone defect is an important factor to be considered in the choice of prosthesis for revision TKA. The varus-valgus constrained prosthesis showed an outcome similar to that of the PS prosthesis. For clinical relevance, varus-valgus constrained prosthesis is recommended in revision TKA when the PS prosthesis seems unsuitable for the management of instability.
III.
本回顾性研究旨在为翻修全膝关节置换术(TKA)中假体的选择提供依据,并评估与后稳定型(PS)假体相比,内翻-外翻限制型假体的疗效。
共 105 例(121 膝)患者接受了翻修 TKA;其中 37 例(42 膝)患者接受了 PS 假体,68 例(79 膝)患者接受了内翻-外翻限制型假体。PS 组和内翻-外翻限制型组的平均随访时间分别为 64.8±31.5 个月和 63.2±28.1 个月。假体选择的标准是术者术中评估的主观松弛度。采用多因素分析评估假体选择的术前因素。
股骨骨缺损程度是影响假体选择的唯一因素。两组患者术后临床疗效均显著改善。两组间临床疗效无显著差异。PS 组并发症发生率为 9.5%,内翻-外翻限制型组为 10.1%,Kaplan-Meier 生存分析显示 PS 组和内翻-外翻限制型组的 8 年组件生存率分别为 83.1%和 93.0%。
股骨骨缺损是翻修 TKA 假体选择的重要考虑因素。内翻-外翻限制型假体的疗效与 PS 假体相似。对于临床相关性,当 PS 假体似乎不适合不稳定的处理时,建议在翻修 TKA 中使用内翻-外翻限制型假体。
III 级。