Handl M, Trc T, Hanus M, Stastný E, Fricová-Poulová M, Neuwirth J, Adler J, Havranová D, Varga F
Ortopedická Klinika Detí a Dospelých 2. LF UK a FN Motol, Praha.
Acta Chir Orthop Traumatol Cech. 2006 Dec;73(6):373-9.
The aim of this study was to present the results of treatment of deep chondral defects of the patella by transplantation of a solid chondral graft formed by autologous cultured chondrocytes.
Indications for autologous chondrocyte implantation most frequently included acute trauma to the knee, particularly the patella, which resulted in a severe focal cartilage defect. The lesions were assessed on the basis of the Bessette and Hunter classification preoperatively, and on the Outerbridge classification during arthroscopy. A sample of healthy cartilage was harvested from a non-weight-bearing area of the trochlea femoris. After cultivation of chondrocytes for 28 to 42 days in the tissue bank, a solid chondral graft, prepared with the use of fibrin glue (Tissucol), was ready for implantation.
Six patients, two males and four females (average age, 21.1 years; range, 13 to 39 years) were treated by this method in the period from July 2003 to October 2005. Follow-up ranged from 1 to 25 months, with an average of 18.5 months. The patients were examined postoperatively by magnetic resonance imaging (MRI) at 2 weeks, 2 and 6 months, and at 1 year. The clinical results were evaluated by the Meyers, the Tegner and the Lysholm knee scoring systems. Two of the six patients, in whom the follow-up period was shorter than 6 months, were not included in the evaluation.
A significant improvement in knee function was recorded when the preoperative and final follow-up stages were compared, as well as on comparison with the healthy contralateral knee joint. MRI examination showed good graft incorporation in all patients.
本研究旨在呈现通过自体培养软骨细胞形成的实体软骨移植物移植治疗髌骨深层软骨缺损的结果。
自体软骨细胞植入的适应症最常见的包括膝关节,尤其是髌骨的急性创伤,导致严重的局灶性软骨缺损。术前根据贝塞特和亨特分类法评估病变,关节镜检查时根据外布里奇分类法评估。从股骨滑车的非负重区域采集健康软骨样本。在组织库中培养软骨细胞28至42天后,使用纤维蛋白胶(Tissucol)制备的实体软骨移植物即可用于植入。
2003年7月至2005年10月期间,6例患者(2例男性,4例女性,平均年龄21.1岁,范围13至39岁)接受了该方法治疗。随访时间为1至25个月,平均18.5个月。术后分别于2周、2个月、6个月及1年行磁共振成像(MRI)检查。临床结果采用迈尔斯、泰格纳和利绍姆膝关节评分系统进行评估。6例患者中有2例随访时间短于6个月,未纳入评估。
术前与最终随访阶段比较,以及与对侧健康膝关节比较,膝关节功能均有显著改善。MRI检查显示所有患者移植物融合良好。