Department of Orthopaedic Surgery, Kyung-Hee University Hospital, Seoul, Republic of Korea.
Department of Orthopaedic Surgery, School of Medicine, Ewha Womans University, Seoul, Republic of Korea.
Cartilage. 2021 Dec;13(1_suppl):1092S-1104S. doi: 10.1177/1947603520921448. Epub 2020 Jun 1.
To compare the efficacy and safety of costal chondrocyte-derived pellet-type autologous chondrocyte implantation (CCP-ACI) with microfracture (MFx) for repair of articular cartilage defects of the knee.
Thirty subjects with an International Cartilage Repair Society (ICRS) grade 3 to 4 chondral defect (2-10 cm in area; ≤4 cm in volume) were randomized at a ratio of 2:1 (CCP-ACI:MFx). Twenty patients were allocated in the CCP-ACI group and 10 patients in the MFx group. CCP-ACI was performed by harvesting costal cartilage at least 4 weeks before surgery. Implantation was performed without any marrow stimulation. Efficacy and safety were assessed at weeks 8, 24, and 48 after surgery according to the magnetic resonance observation of cartilage repair tissue (MOCART) score and clinical outcomes.
MOCART scores improved from baseline to 24 and 48 weeks postoperatively in both treatment groups. The improvement in MOCART scores in the CCP-ACI group was significantly greater than that in the MFx group at 24 and 48 weeks (39.1 vs 21.8 and 43.0 vs 24.8, respectively). The proportions of complete defect repair and complete integration were significantly higher in the CCP-ACI group than the MFx group at 48 weeks. Improvement in Lysholm score and KOOS subscores, including Function (Sports and Recreational Activity) and knee-related quality of life was significantly greater in the CCP-ACI group than the MFx group at 48 weeks (35.4 vs 31.5, 35.7 vs 28.5, and 27.9 vs 11.6, respectively).
Treatment of cartilage defects with CCP-ACI yielded satisfactory cartilage tissue repair outcomes, with good structural integration with native cartilage tissue shown by magnetic resonance imaging at 24 and 48 weeks after surgery.
Level 1: Randomized controlled study.
比较肋软骨源性微球型自体软骨细胞移植(CCP-ACI)与微骨折(MFx)治疗膝关节软骨缺损的疗效和安全性。
30 例国际软骨修复协会(ICRS)3 至 4 级软骨缺损患者(面积 2-10cm,容积≤4cm)按 2:1(CCP-ACI:MFx)随机分组。20 例患者分入 CCP-ACI 组,10 例患者分入 MFx 组。CCP-ACI 在手术前至少 4 周采集肋软骨。植入时不进行任何骨髓刺激。术后 8、24 和 48 周根据磁共振软骨修复组织观察评分(MOCART)和临床结果评估疗效和安全性。
两组患者的 MOCART 评分均从基线提高到术后 24 和 48 周。CCP-ACI 组 MOCART 评分的改善在术后 24 和 48 周均显著大于 MFx 组(分别为 39.1 比 21.8 和 43.0 比 24.8)。CCP-ACI 组在术后 48 周时完全修复和完全整合的比例显著高于 MFx 组。在术后 48 周时,CCP-ACI 组的 Lysholm 评分和 KOOS 子评分(包括功能[运动和娱乐活动]和膝关节相关生活质量)的改善显著大于 MFx 组(分别为 35.4 比 31.5、35.7 比 28.5 和 27.9 比 11.6)。
CCP-ACI 治疗软骨缺损可获得满意的软骨组织修复效果,术后 24 和 48 周时磁共振成像显示与天然软骨组织具有良好的结构整合。
1 级:随机对照研究。