Department of Orthopaedic Surgery, Rush University Medical Center, Chicago, Illinois, United States.
Department of Orthopaedic Surgery, Rush University Medical Center, Chicago, Illinois, United States.
Knee. 2022 Aug;37:162-170. doi: 10.1016/j.knee.2022.04.003. Epub 2022 Jul 6.
The aim of this study was to evaluate the radiographic and clinical outcomes of a recently introduced metaphyseal cone system for revision TKA.
73 revision TKAs in 72 patients were retrospectively reviewed. All patients had a minimum of 2-year clinical follow-up (mean 34.1 months; range 24.0 to 50.3 months). 114 Metaphyseal cones (64 tibial and 50 femoral) of a single manufacturer were implanted. The most common indications for revision were aseptic loosening (56.9%), second stage reimplantation for periprosthetic joint infection (PJI; 26.4%), and instability (12.5%). All femoral and tibial stems were press-fit cementless stems.
Ten of 72 patients underwent re-revision: six for infection (8.3%), two for instability (2.8%), one (1.4%) for patellar tendon rupture and one (1.4%) for femoral component loosening (a cone was not utilized at index revision). Two patients had loose cones (one with an isolated tibial cone and one with both femoral and tibial cones) associated with loose implants but declined re-revision. Aseptic survivorship of our patient cohort free from any re-revision surgery was 95.9% at 2 years (95% CI 87.4-98.7%) and 96.5% of cones demonstrated radiographic evidence of osseointegration. At 2-years, the Knee Society Score (KSS) improved from a mean of 17.2 points preoperatively to 57.8 points (p <.0001).
Porous-coated metaphyseal cones from this manufacturer demonstrate excellent aseptic survivorship and radiographic evidence of osseointegration similar to prior designs when used with cementless stems.
本研究旨在评估最近引入的用于翻修 TKA 的干骺端锥形系统的影像学和临床结果。
回顾性分析了 72 例 73 例翻修 TKA 患者的资料。所有患者均获得至少 2 年的临床随访(平均随访 34.1 个月;范围 24.0 至 50.3 个月)。植入了单一制造商的 114 个干骺端锥形物(64 个胫骨和 50 个股骨)。翻修的最常见指征为无菌性松动(56.9%)、二期再植入治疗假体周围关节感染(PJI;26.4%)和不稳定(12.5%)。所有股骨和胫骨柄均为压配非骨水泥柄。
72 例患者中有 10 例再次翻修:6 例因感染(8.3%),2 例因不稳定(2.8%),1 例(1.4%)因髌腱断裂和 1 例(1.4%)因股骨组件松动(初次翻修时未使用锥形物)。有 2 例锥形物松动(1 例胫骨锥形物单独松动,1 例股骨和胫骨锥形物均松动),但与松动的植入物相关,且患者拒绝再次翻修。2 年时,无任何再次翻修手术的患者的无菌生存率为 95.9%(95%CI 87.4-98.7%),96.5%的锥形物显示出影像学骨整合证据。2 年时,膝关节协会评分(KSS)从术前平均 17.2 分提高到 57.8 分(p<.0001)。
与之前的设计相比,当与非骨水泥柄一起使用时,该制造商生产的多孔涂层干骺端锥形物具有极好的无菌生存率和影像学骨整合证据。