Rush University Medical Center, Chicago, Illinois, USA.
Mayo Clinic, Rochester, Minnesota, USA.
Am J Sports Med. 2024 Aug;52(10):2547-2554. doi: 10.1177/03635465241261353. Epub 2024 Aug 5.
Osteochondral allograft (OCA) transplantation is an important surgical technique for full-thickness chondral defects in the knee. For patients undergoing this procedure, topography matching between the donor and recipient sites is essential to limit premature wear of the OCA. Currently, there is no standardized process of donor and recipient graft matching.
To evaluate a novel topography matching technique for distal femoral condyle OCA transplantation using 3-dimensional (3D) laser scanning to create 3D-printed patient-specific instrumentation in a human cadaveric model.
Descriptive laboratory study.
Human cadaveric distal femoral condyles (n = 12) underwent 3D laser scanning. An 18-mm circular osteochondral recipient defect was virtually created on the medial femoral condyle (MFC), and the position and orientation of the best topography-matched osteochondral graft from a paired donor lateral femoral condyle (LFC) were determined using an in silico analysis algorithm minimizing articular step-off distances between the edges of the graft and recipient defect. Distances between the entire surface of the OCA graft and the underneath surface of the MFC were evaluated as surface mismatch. Donor (LFC) and recipient (MFC) 3D-printed patient-specific guides were created based on 3D reconstructions of the scanned condyles. Through use of the guides, OCAs were harvested from the LFC and transplanted to the reamed recipient defect site (MFC). The post-OCA recipient condyles were laser scanned. The 360° articular step-off and cartilage topography mismatch were measured.
The mean cartilage step-off and graft surface mismatch for the in silico OCA transplant were 0.073 ± 0.029 mm (range, 0.005-0.113 mm) and 0.166 ± 0.039 mm (range, 0.120-0.243 mm), respectively. Comparatively, the cadaveric specimens postimplant had significantly larger step-off differences (0.173 ± 0.085 mm; range, 0.082-0.399 mm; = .001) but equivalent graft surface topography matching (0.181 ± 0.080 mm; range, 0.087-0.396 mm; = .678). All 12 OCA transplants had mean circumferential step-off differences less than a clinically significant cutoff of 0.5 mm.
These findings suggest that the use of 3D-printed patient-specific guides for OCA transplantation has the ability to reliably optimize cartilage topography matching for LFC to MFC transplantation. This study demonstrated substantially lower step-off values compared with previous orthopaedic literature when also evaluating LFC to MFC transplantation. Using this novel technique in a model performing MFC to MFC transplantation has the potential to yield further enhanced results due to improved radii of curvature matching.
Topography-matched graft implantation for focal chondral defects of the knee in patients improves surface matching and has the potential to improve long-term outcomes. Efficient selection of the allograft also allows improved availability of the limited allograft sources.
骨软骨同种异体移植(OCA)是治疗膝关节全层软骨缺损的重要手术技术。对于接受该手术的患者,供体和受区之间的形貌匹配对于限制 OCA 的早期磨损至关重要。目前,还没有标准化的供体和受区移植物匹配过程。
使用三维(3D)激光扫描评估一种新的用于股骨远端髁 OCA 移植的形貌匹配技术,以创建 3D 打印的患者特定器械在人体尸体模型中。
描述性实验室研究。
对 12 个人体尸体股骨远端髁进行 3D 激光扫描。在股骨内侧髁(MFC)上虚拟创建了一个 18mm 的圆形骨软骨受区缺损,使用最小化移植物和受区缺损边缘关节台阶距离的虚拟分析算法确定来自配对供体外侧髁(LFC)的最佳形貌匹配的骨软骨移植物的位置和方向。评估 OCA 移植物整个表面与 MFC 底面之间的距离作为表面不匹配。根据扫描髁的 3D 重建,创建了供体(LFC)和受体(MFC)的 3D 打印患者特定的导向器。通过使用这些导向器,从 LFC 中采集 OCA 并移植到扩孔的受区缺损部位(MFC)。激光扫描移植后 OCA 的受区髁。测量了 360°关节台阶和软骨形貌不匹配。
计算机模拟 OCA 移植的平均软骨台阶和移植物表面不匹配分别为 0.073±0.029mm(范围 0.005-0.113mm)和 0.166±0.039mm(范围 0.120-0.243mm)。相比之下,植入后的尸体标本具有明显更大的台阶差异(0.173±0.085mm;范围 0.082-0.399mm; =.001),但移植的移植物表面形貌匹配相同(0.181±0.080mm;范围 0.087-0.396mm; =.678)。所有 12 个 OCA 移植的平均周向台阶差异均小于 0.5mm 的临床显著截定点。
这些发现表明,使用 3D 打印的患者特定导向器进行 OCA 移植具有可靠地优化 LFC 到 MFC 移植的软骨形貌匹配的能力。与评估 LFC 到 MFC 移植的先前骨科文献相比,本研究显示出明显较低的台阶值。在进行 MFC 到 MFC 移植的模型中使用这种新的技术,由于曲率匹配的改善,有可能进一步提高结果。
对于膝关节局灶性软骨缺损的患者,进行形貌匹配的移植物植入可以改善表面匹配,并有可能改善长期结果。同种异体移植物的有效选择还允许更好地利用有限的同种异体移植物来源。