McCarrel Taralyn M, Pownder Sarah L, Gilbert Susannah, Koff Matthew F, Castiglione Emme, Saska Ryan A, Bradica Gino, Fortier Lisa A
1 Department of Clinical Sciences, Cornell University College of Veterinary Medicine, Ithaca, NY, USA.
Department of Large Animal Clinical Sciences, University of Florida College of Veterinary Medicine, Gainesville, FL, USA.
Cartilage. 2017 Oct;8(4):406-416. doi: 10.1177/1947603516675913. Epub 2016 Nov 4.
Objective To evaluate a biphasic cartilage repair device (CRD) for feasibility of arthroscopic implantation, safety, biocompatibility, and efficacy for long-term repair of large osteochondral defects. Methods The CRD was press-fit into defects (10 mm diameter, 10 mm deep) created in the femoral trochlea of 12 horses. In the contralateral limb, 10 mm diameter full-thickness chondral defects were treated with microfracture (MFX). Radiographs were obtained pre- and postoperatively, and at 4, 12, and 24 months. Repeat arthroscopy was performed at 4 and 12 months. Gross assessment, histology, mechanical testing, and magnetic resonance imaging (MRI) were performed at 24 months. Results The CRD was easily placed arthroscopically. There was no evidence of joint infection, inflammation, or degeneration. CRD-treated defects had significantly more sclerosis compared to MFX early ( P = 0.0006), but was not different at 24 months. CRD had better arthroscopic scores at 4 months compared to MFX ( P = 0.0069). At 24 months, there was no difference in repair tissue on histology or mechanical testing. Based on MRI, CRD repair tissue had less proteoglycan (deep P = 0.027, superficial P = 0.015) and less organized collagen (deep P = 0.028) compared to MFX. Cartilage surrounding MFX defects had more fissures compared to CRD. Conclusion The repair tissue formed after CRD treatment of a large osteochondral lesion is fibrocartilage similar to that formed in simple chondral defects treated with MFX. The CRD can be easily placed arthroscopically, is safe, and biocompatible for 24 months. The CRD results in improved early arthroscopic repair scores and may limit fissure formation in adjacent cartilage.
目的 评估一种双相软骨修复装置(CRD)用于关节镜植入的可行性、安全性、生物相容性以及对大的骨软骨缺损进行长期修复的疗效。方法 将CRD压配入12匹马股骨滑车中制造的缺损(直径10毫米,深10毫米)。在对侧肢体,直径10毫米的全层软骨缺损采用微骨折术(MFX)治疗。在术前、术后以及4、12和24个月时拍摄X线片。在4个月和12个月时进行重复关节镜检查。在24个月时进行大体评估、组织学检查、力学测试以及磁共振成像(MRI)。结果 CRD易于通过关节镜置入。没有关节感染、炎症或退变的证据。与早期MFX治疗相比,CRD治疗的缺损硬化明显更多(P = 0.0006),但在24个月时无差异。与MFX相比,CRD在4个月时关节镜评分更好(P = 0.0069)。在24个月时,组织学或力学测试的修复组织无差异。基于MRI,与MFX相比,CRD修复组织蛋白聚糖较少(深层P = 0.027,浅层P = 0.015)且胶原排列较差(深层P = 0.028)。与CRD相比,MFX缺损周围的软骨有更多裂隙。结论 用CRD治疗大的骨软骨损伤后形成的修复组织是纤维软骨,类似于用MFX治疗的单纯软骨缺损中形成的纤维软骨。CRD可通过关节镜轻松置入,安全且24个月内具有生物相容性。CRD可提高早期关节镜修复评分,并可能限制相邻软骨的裂隙形成。