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No implant migration and good subjective outcome of a novel customized femoral resurfacing metal implant for focal chondral lesions

机译:对于局灶性软骨病变,新型定制股骨表面重修金属植入物没有植入物迁移和良好的主观结果

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摘要

Purpose: Managing focal cartilage injuries in the middle-aged patient poses a challenge. Focal prosthetic inlay resurfacing has been proposed to be a bridge between biologics and conventional joint arthroplasty. Patient selection and accurate implant positioning is crucial to avoid increased contact pressure to the opposite cartilage surface. A customized femoral condyle implant for focal cartilage injuries was designed to precisely fit each patient’s individual size and location of damage. The primary objective was to assess implant safety profile, surgical usability of the implant and instruments, and implant migration with radiostereometric analysis (RSA). Methods: Ten patients 36–56 years with focal chondral defects, ICRS 3–4 of the femoral cartilage and failed earlier conservative or surgical interventions with VAS pain > 40. The patients were followed for 2 years with subjective outcome measures (VAS, EQ5D, KOOS) and RSA. The customized implant and guide instruments were manufactured by computer-aided design/computer-aided manufacturing (CAD/CAM) techniques using MRI data. Results: VAS, EQ5D and KOOS showed improvements that reached significance for VAS (p ≤ 0.001), Tegner (p = 0.034) and the KOOS subscores ADL (p = 0.0048), sport and recreation (p = 0.034) and quality of life (p = 0.037). VAS and KOOS scores improved gradually at 3, 6 and 12 months. The improvements in EQ5D, KOOS pain and KOOS symptoms did not reach statistical significance. No infections, deep venous thrombosis or other complications occured in the postoperative period. No radiographic signs of damage to the opposing tibial cartilage was noted. The surgical usability of implants and instruments were good. RSA did not show any implant migration. Conclusion: This is the first clinical report of a new customized, focal knee resurfacing system. The short-term implant safety and patient-related outcome measures showed good-to-excellent results. Level of evidence: Prospective case series, Level 4.
机译:目的:控制中年人的局部软骨损伤是一个挑战。人工修复的嵌体表面修复已被提议是生物制剂和常规关节置换术之间的桥梁。患者选择和准确的植入物定位对于避免增加与相对的软骨表面的接触压力至关重要。专门设计用于关节软骨损伤的定制股骨focal植入物,以精确适合每个患者的个体大小和损伤部位。主要目的是通过放射立体分析(RSA)评估植入物的安全性,植入物和器械的手术可用性以及植入物的迁移。方法:10例36-56岁的局灶性软骨缺损,股骨软骨的ICRS 3–4以及较早的保守或手术干预失败,且VAS疼痛>40。对这些患者进行了2年的主观预后评估(VAS,EQ5D, KOOS)和RSA。定制的植入物和引导器械是使用MRI数据通过计算机辅助设计/计算机辅助制造(CAD / CAM)技术制造的。结果:VAS,EQ5D和KOOS显示出改善,对VAS(p≤0.001),Tegner(p = 0.034)和KOOS分数ADL(p = 0.0048),运动和休闲(p = 0.034)和生活质量( p = 0.037)。在3、6和12个月时,VAS和KOOS评分逐渐提高。 EQ5D,KOOS疼痛和KOOS症状的改善没有达到统计学意义。术后无感染,深静脉血栓形成或其他并发症发生。没有发现对相对的胫骨软骨损伤的放射学迹象。植入物和器械的手术可用性良好。 RSA没有显示出任何植入物迁移。结论:这是新的定制的,局部膝关节表面置换系统的第一份临床报告。短期种植体安全性和与患者相关的结果指标显示了良好的效果。证据级别:预期案例系列,级别4。

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