Schüttler Karl-Friedrich, Götschenberg A, Klasan A, Stein T, Pehl A, Roessler P P, Figiel J, Heyse T J, Efe T
Centre for Orthopedics and Trauma surgery, University Hospital Marburg, 35043, Marburg, Germany.
Department of Sporttraumatology, Knee-and Shoulder-Surgery, Berufsgenossenschaftliche Unfallklinik Frankfurt am Main, Frankfurt, Germany.
Arch Orthop Trauma Surg. 2019 Jan;139(1):99-106. doi: 10.1007/s00402-018-3028-4. Epub 2018 Aug 18.
Cartilage defects of the knee remain a challenging problem in orthopedic surgery despite the ongoing improvements in regenerative procedures such as the autologous chondrocyte transplantation. Due to the lack of donor-site morbidity and the single-stage procedure cell-free scaffolds are an interesting alternative to cell-based procedures. But as currently mid- and long-term data are lacking, the aim of the present study was to present mid-term clinical, radiological and histological results of a cell-free collagen type I scaffolds for cartilage repair.
Twenty-eight patients were followed prospectively. Clinical evaluation using patient-reported outcome measures (KOOS, IKDC; VAS for pain, Tegner score for activity) as well as radiologic evaluation of the repair tissue (MOCART) was performed at 1 year, 2 years and 5 years. Histologic evaluation of the repair tissue was done in case of revision surgery using the ICRS II score for human cartilage repair.
In these large cartilage defects with a mean defect size of 3.7 ± 1.9 cm, clinical failure necessitating revision surgery was seen in 5 of 28 patients (18%). While the remaining patients showed good-to-excellent clinical results (KOOS, IKDC, VAS, Tegner), the radiologic appearance of the repair tissue showed a reduction of the MOCART score between the 2- and 5-year follow-up. Histologic evaluation of the repair tissue showed a cartilage-like appearance with no signs of inflammation or cell death but an overall medium tissue quality according to the ICRS II Score.
The use of this cell-free collagen type I scaffold for large defects showed increased wear of the repair tissue and clinical failure in 18% of cases at 5-year follow-up.
尽管自体软骨细胞移植等再生手术不断改进,但膝关节软骨缺损在骨科手术中仍然是一个具有挑战性的问题。由于不存在供体部位并发症且为单阶段手术,无细胞支架是基于细胞的手术的一个有趣替代方案。但由于目前缺乏中长期数据,本研究的目的是展示用于软骨修复的无细胞I型胶原蛋白支架的中期临床、放射学和组织学结果。
对28例患者进行前瞻性随访。在1年、2年和5年时使用患者报告结局指标(膝关节损伤和骨关节炎疗效评分、国际膝关节文献委员会评分;疼痛视觉模拟评分、活动度的泰格纳评分)进行临床评估,并对修复组织进行放射学评估(改良的磁共振成像观察软骨修复组织评分)。在翻修手术时,使用国际软骨修复协会II级评分对修复组织进行组织学评估。
在这些平均缺损大小为3.7±1.9厘米的大软骨缺损中,28例患者中有5例(18%)出现临床失败,需要进行翻修手术。虽然其余患者的临床结果为良好至优秀(膝关节损伤和骨关节炎疗效评分、国际膝关节文献委员会评分、疼痛视觉模拟评分、泰格纳评分),但修复组织的放射学表现显示,在2年和5年随访之间改良的磁共振成像观察软骨修复组织评分有所降低。修复组织的组织学评估显示其外观类似软骨,没有炎症或细胞死亡迹象,但根据国际软骨修复协会II级评分,整体组织质量中等。
对于大缺损使用这种无细胞I型胶原蛋白支架,在5年随访时显示修复组织磨损增加,18%的病例出现临床失败。