Meier E, Gelse K, Trieb K, Pachowsky M, Hennig F F, Mauerer A
Department of Orthopaedic and Trauma Surgery, University Hospital Erlangen, Krankenhausstr. 12, 91054, Erlangen, Germany.
Hospital Wels, Grieskirchnerstr. 42, A-4600, Wels, Austria.
J Orthop Surg Res. 2016 Feb 8;11:21. doi: 10.1186/s13018-016-0352-7.
The aim of the study was to evaluate the safety and efficacy of a novel metal-free ceramic total knee replacement system.
Thirty-eight primary total knee arthroplasties (TKAs) were performed on 34 patients using the metal-free BPK-S ceramic total knee replacement system with both the femoral and tibial components of an alumina/zirconia ceramic composite. The clinical outcome was evaluated pre- and postoperatively at 3 (n = 32 TKA) and 12 months (n = 32 TKA) using the Knee Society Score (KSS), the Oxford Knee Score and the EQ-5D. Safety analysis was performed by radiological examination and assessment of adverse events.
Postoperatively, the KSS, Oxford Knee Score and EQ-5D improved significantly at 3 and 12 months (p < 0.001). Non-progressive partial radiolucent lines were observed in six cases, but there was no osteolysis and no implant loosening. Induction or exacerbation of allergies did not occur during the follow-up.
The metal-free BPK-S ceramic total knee replacement system proved to be a safe and clinically efficient alternative to metal implants in this short-term follow-up study.
本研究的目的是评估一种新型无金属陶瓷全膝关节置换系统的安全性和有效性。
使用由氧化铝/氧化锆陶瓷复合材料制成的股骨和胫骨组件的无金属BPK-S陶瓷全膝关节置换系统,对34例患者进行了38次初次全膝关节置换术(TKA)。使用膝关节协会评分(KSS)、牛津膝关节评分和EQ-5D在术前以及术后3个月(n = 32例TKA)和12个月(n = 32例TKA)时评估临床结果。通过放射学检查和不良事件评估进行安全性分析。
术后,KSS、牛津膝关节评分和EQ-5D在3个月和12个月时均显著改善(p < 0.001)。6例观察到非进行性部分透光线,但未出现骨溶解和植入物松动。随访期间未发生过敏反应的诱发或加重。
在这项短期随访研究中,无金属BPK-S陶瓷全膝关节置换系统被证明是金属植入物的一种安全且临床有效的替代方案。