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首页> 外文期刊>Knee surgery, sports traumatology, arthroscopy: official journal of the ESSKA >Use of cell-free collagen type I matrix implants for the treatment of small cartilage defects in the knee: Clinical and magnetic resonance imaging evaluation
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Use of cell-free collagen type I matrix implants for the treatment of small cartilage defects in the knee: Clinical and magnetic resonance imaging evaluation

机译:使用无细胞的I型胶原蛋白基质植入物治疗膝关节小软骨缺损:临床和磁共振成像评估

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Purpose: Articular cartilage defects of the knee are a common condition for which several repair techniques have been described. The aim of the present study was to assess medium-term results of a one-step procedure using a cell-free collagen type I matrix. Methods: Fifteen patients with articular cartilage defects of the knee were treated with an 11-mm-diameter cell-free collagen type 1 matrix implant. The matrices were implanted in a press-fit manner into the defect after careful debridement down to the subchondral bone but without penetration of this margin. Follow-up examinations were carried out at 6 weeks, 6 months, and at 12, 24, 36, and 48 months after implantation. Clinical assessment included the visual analogue scale (VAS), the Tegner activity scale, and the International Knee Documentation Committee (IKDC) score. Radiological assessment for graft attachment and tissue regeneration was performed using the magnetic observation of cartilage repair tissue (MOCART) score. Results: A total of 15 patients (males: n = 6 and females: n = 9) with a mean age of 26.4 years (range 19-40) were treated. The mean VAS improved significantly when compared to the preoperative values (P < 0.05). Six weeks after implantation, IKDC values were slightly lower than the preoperative values (n.s.), but increased significantly at final follow-up (P < 0.05). At 24 months, there were no significant differences in the median Tegner score between the post-operative values and the preoperative values (n.s.). However, after 36 months, a significant improvement was noted that lasted at least up to 48 months (P < 0.05). The MOCART score improved consistently up to 4 years after implantation, with significant improvements already observed after 12 months (P < 0.05). No correlation between the clinical scores and the MOCART score could be perceived. Conclusion: The present study showed that the use of cell-free collagen type I matrix implants led to a significant and durable improvement in all the clinical and imaging scores investigated 4 years after implantation. Level of evidence: IV.
机译:目的:膝关节软骨缺损是一种常见病状,已针对其描述了几种修复技术。本研究的目的是评估使用无细胞I型胶原基质的一步法的中期结果。方法:15例膝关节软骨缺损患者接受了11毫米直径的无细胞1型胶原蛋白基质植入物的治疗。仔细清创至软骨下骨后,将基质以压入配合的方式植入缺损处,但不能穿透该边缘。植入后6周,6个月和12、24、36和48个月进行了随访检查。临床评估包括视觉模拟量表(VAS),Tegner活动量表和国际膝关节文献委员会(IKDC)得分。使用软骨修复组织(MOCART)评分的磁性观察对移植物附着和组织再生进行放射学评估。结果:共治疗了15例平均年龄为26.4岁(19-40岁)的患者(男:n = 6,女:n = 9)。与术前相比,平均VAS显着改善(P <0.05)。植入后六周,IKDC值略低于术前值(n.s.),但在最终随访时明显增加(P <0.05)。在第24个月时,手术后数值与术前数值(n.s.)之间的中位Tegner评分无显着差异。但是,在36个月后,观察到显着改善,至少持续48个月(P <0.05)。植入后直至4年,MOCART评分一直持续改善,在12个月后已观察到显着改善(P <0.05)。临床评分与MOCART评分之间没有相关性。结论:本研究表明,使用无细胞I型胶原基质植入物可显着持久地改善植入后4年的所有临床和影像学评分。证据级别:IV。

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