From the Department of Surgery, Section of Orthopaedic Surgery, University of Manitoba, Winnipeg, Man. (Perrin, Turgeon); and the Concordia Joint Replacement Group, Concordia Hip & Knee Institute, Winnipeg, Man. (Turgeon).
Can J Surg. 2020 May 1;63(3):E196-E201. doi: 10.1503/cjs.002419.
Literature on the survival rates and function of hinged total knee replacement (HTKR) prostheses is scarce, and to our knowledge there is not yet any published literature on the Legion HK Hinge Knee Replacement prosthesis (Smith & Nephew) with guided-motion articulation. The objective of this study was to establish the early survival rate of this modern HTKR at a single institution and to investigate postoperative patient function and satisfaction.
This retrospective study included patients who received the Legion HTKR prosthesis with guided-motion inserts as a primary or revision implant between October 11 and March 2016 at a tertiary care centre in Manitoba, Canada. Preoperative and postoperative functional scores on the 12-item Oxford Knee Score and postoperative patient satisfaction were assessed.
Thirty-nine HTKR implantations (38 patients) were included in this study: 12 primary cases and 27 revision cases. Three revision surgeries and 4 perioperative complications were noted at a mean follow-up of 29.1 months. The 2-year survivorship of the HTKR system was 90.7%. Postoperative functional scores improved significantly and the majority of patients were satisfied or very satisfied at all follow-up time points.
The early survival rate of a modern guided-motion HTKR prosthesis is similar to the survival rates of other hinged knee prostheses published in the literature. The prosthesis demonstrated substantial postoperative functional improvement when used in the setting of complex primary or revision total knee replacement.
铰链式全膝关节置换术(HTKR)假体的生存率和功能的相关文献很少,据我们所知,目前还没有关于带有导向运动关节的 Legion HK 铰链膝关节置换假体(Smith & Nephew)的发表文献。本研究的目的是在一家机构确定这种现代 HTKR 的早期生存率,并研究术后患者的功能和满意度。
本回顾性研究纳入了 2016 年 10 月 11 日至 3 月期间在加拿大马尼托巴省的一家三级护理中心接受 Legion HTKR 假体(带导向插入物)作为初次或翻修植入物的患者。评估了术前和术后的 12 项牛津膝关节评分(Oxford Knee Score)的功能评分以及术后患者满意度。
本研究共纳入 39 例 HTKR 植入物(38 例患者):初次植入 12 例,翻修植入 27 例。在平均 29.1 个月的随访中,有 3 例翻修手术和 4 例围手术期并发症。HTKR 系统的 2 年生存率为 90.7%。术后功能评分显著改善,大多数患者在所有随访时间点都表示满意或非常满意。
现代导向运动 HTKR 假体的早期生存率与文献中公布的其他铰链膝关节假体的生存率相似。该假体在复杂的初次或翻修全膝关节置换术中具有显著的术后功能改善。