Kim Jong-Min, Kim Sang-Beom, Kim Jong-Min, Lee Dae-Hee, Lee Bum-Sik, Bin Seong-Il
Department of Orthopaedic Surgery, Kosin University Gospel Hospital, Busan, Korea.
Department of Orthopaedic Surgery, Asan Medical Center, Seoul, Korea.
Knee Surg Relat Res. 2015 Mar;27(1):17-23. doi: 10.5792/ksrr.2015.27.1.17. Epub 2015 Mar 2.
To compare the incidence of overhang between two distinct femoral components and whether there is clinical and radiological benefit of gender-specific implants in short-term follow-up.
One hundred and four knees in consecutive 66 female patients who underwent primary total knee arthroplasty due to primary osteoarthritis were included in this study. Overhang was measured and recorded in every cut surface of femur with both gender-specific and traditional trial femoral components respectively in every patient. Then, the knees were divided into two groups according to the type of the permanent femoral component they received. Clinical and radiological outcomes were compared between 2 groups at minimum 3 years after operation.
Mean follow-up duration was 41.3 months (range, 36 to 50 months). Sixty two knees (59.6%) showed femoral overhang at least in one area with a traditional trial component, while 26 knees (25.0%) did with a gender-specific trial component (p<0.001). In terms of range of motion, Hospital for Special Surgery knee score, radiographic result, patella tilt angle and displacement, no significant difference was observed between two groups.
The use of gender-specific implants substantially reduced the incidence of femoral overhang but did not demonstrate any clinical, functional or radiologic benefit in short-term follow-up.
比较两种不同股骨假体的悬突发生率,以及在短期随访中,特定性别的植入物是否具有临床和影像学益处。
本研究纳入了66例因原发性骨关节炎接受初次全膝关节置换术的连续女性患者的104个膝关节。在每位患者中,分别使用特定性别的和传统的试验性股骨假体,在股骨的每个切割面上测量并记录悬突情况。然后,根据患者所接受的永久性股骨假体类型将膝关节分为两组。在术后至少3年时比较两组的临床和影像学结果。
平均随访时间为41.3个月(范围36至50个月)。62个膝关节(59.6%)使用传统试验性假体时至少在一个区域出现股骨悬突,而使用特定性别的试验性假体时为26个膝关节(25.0%)(p<0.001)。在活动范围、特种外科医院膝关节评分、影像学结果、髌骨倾斜角度和移位方面,两组之间未观察到显著差异。
使用特定性别的植入物可大幅降低股骨悬突的发生率,但在短期随访中未显示出任何临床、功能或影像学益处。