The Joint Replacement Center, Ewha Womans University School of Medicine, MokDong Hospital, 911-1, MokDong, YangChun-Ku, Seoul, Republic of Korea (158-710). E-mail address for Y.-H. Kim:
J Bone Joint Surg Am. 2014 Nov 5;96(21):1807-13. doi: 10.2106/JBJS.M.01605.
We are not aware of any information on in vivo clinical results at a minimum of five years after posterior cruciate-substituting total knee arthroplasties performed with a highly cross-linked polyethylene insert. The purpose of the study was to evaluate whether the clinical and radiographic results of posterior cruciate-substituting total knee prostheses, including the prevalences of fracture of the polyethylene post, failure of the locking mechanism of the tibial polyethylene insert, and osteolysis, would be similar between patients treated with conventional polyethylene and those treated with highly cross-linked polyethylene.
Three hundred and eight patients with a mean age of 60.3 years (range, twenty-two to sixty-five years) received a posterior cruciate-substituting total knee prosthesis with a conventional polyethylene tibial insert in one knee and the same prosthesis with a highly cross-linked polyethylene tibial insert in the contralateral knee. Twenty patients were men and 288 were women. The mean duration of follow-up was 5.9 years (range, five to 6.8 years). At each follow-up visit, the patients were assessed radiographically and clinically with the rating system of the Knee Society; the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC); and the University of California, Los Angeles (UCLA) activity score.
The two groups did not differ significantly (p > 0.05) with regard to the mean postoperative Knee Society total knee scores (93.5 compared with 93.7 points), function scores (82.9 compared with 82.7 points), and pain scores (46.7 compared with 47.1 points); WOMAC scores (16 compared with 15 points); range of motion (129.7° compared with 130.1°); or patient satisfaction assessed with a visual analog scale (7.6 compared with 7.9 points). The mean UCLA activity score was 6.4 points (p > 0.05). There were no significant differences between the two groups with regard to radiographic results. No knee in either group had a fracture of the tibial polyethylene post or failure of the locking mechanism of the tibial polyethylene insert. No knee in either group had osteolysis. One knee (0.3%), treated with highly cross-linked polyethylene, was revised because of infection.
The data suggest that clinical and radiographic findings at five years after posterior cruciate-substituting total knee arthroplasty were the same for the patients treated with highly cross-linked polyethylene and those treated with conventional polyethylene.
我们不了解任何关于使用高度交联聚乙烯插入物进行后交叉韧带替代全膝关节置换术后至少五年的体内临床结果的信息。本研究的目的是评估后交叉韧带替代全膝关节假体的临床和影像学结果,包括聚乙烯后柱骨折、胫骨聚乙烯插入物锁定机制失效和溶骨性疾病的患病率,在接受传统聚乙烯治疗的患者和接受高度交联聚乙烯治疗的患者之间是否相似。
308 名平均年龄为 60.3 岁(22-65 岁)的患者在一侧膝关节中接受了后交叉韧带替代的全膝关节假体,使用传统聚乙烯胫骨插入物,在对侧膝关节中接受了相同的假体和高度交联聚乙烯胫骨插入物。20 名男性和 288 名女性。平均随访时间为 5.9 年(5-6.8 年)。每次随访时,使用膝关节协会评分系统、安大略省和麦克马斯特大学骨关节炎指数(WOMAC)和加利福尼亚大学洛杉矶分校(UCLA)活动评分对患者进行影像学和临床评估。
两组在术后平均膝关节协会总膝关节评分(93.5 分比 93.7 分)、功能评分(82.9 分比 82.7 分)和疼痛评分(46.7 分比 47.1 分)、WOMAC 评分(16 分比 15 分)、运动范围(129.7°比 130.1°)或视觉模拟评分评估的患者满意度(7.6 分比 7.9 分)方面差异均无统计学意义(p>0.05)。平均 UCLA 活动评分(6.4 分,p>0.05)。两组在影像学结果方面无显著差异。两组均未发生胫骨聚乙烯后柱骨折或胫骨聚乙烯插入物锁定机制失效。两组均未发生溶骨性疾病。1 例(0.3%)膝关节采用高度交联聚乙烯治疗后因感染而翻修。
数据表明,在后交叉韧带替代全膝关节置换术后五年时,接受高度交联聚乙烯治疗的患者和接受传统聚乙烯治疗的患者的临床和影像学结果相同。