Washington University, Department of Orthopaedic Surgery, St. Louis, MO, U.S.A.
OrthoCarolina, Charlotte, NC, U.S.A.
Arthroscopy. 2019 Apr;35(4):1212-1218. doi: 10.1016/j.arthro.2018.11.017. Epub 2019 Mar 11.
The purpose of the study is to assess the stability of a dehydrated cartilage allograft combined with platelet-rich plasma sealed with fibrin glue within trochlear and medial femoral condyle (MFC) chondral defects in a cadaver knee model.
Defects were made in the trochlea (20, 25, and 30 mm) and MFC (15, 20, and 25 mm) of 6 cadaver specimens. Allograft was applied utilizing 2 different techniques: (1) proud in which the fibrin level extends beyond surrounding cartilage and (2) recessed in which the fibrin level is even with or below the surrounding cartilage. The knees were cycled by using a continuous passive motion machine through a range of motion. Defects were assessed for superficial delamination and displacement of the allograft. This was quantified as the percentage of surface delamination and/or exposed bone. Comparisons were made with regard to defect size, location, and fill.
In both the MFC and trochlea, proud application resulted in an increased rate of fibrin delamination. In the trochlea, an average of 38% delamination was detected in the recessed 20-mm defect compared with 70% in the proud 30-mm defect (P < .05). This effect was increased with increasing defect size. In the MFC, mean delamination of 43% and 28% exposed bone was noticed in the proud 15-mm defect compared with 95% delamination and 71% exposed bone at 25 mm. In 82% of specimens, displacement and/or delamination occurred within the first 15 minutes of testing.
Increased defect size in both the trochlea and femoral condyle, as well as a proud construct application, were associated with significant delamination and displacement of the allograft/fibrin construct.
Proud application of allograft increases the likelihood of fibrin delamination and graft displacement in both trochlear and MFC defects. This effect is increased with increasing defect size. These data may support limiting range of motion immediately after an allograft procedure.
本研究旨在评估脱水软骨移植物与富含血小板的血浆结合纤维蛋白胶在尸体膝关节模型滑车和内侧股骨髁(MFC)软骨缺损中的稳定性。
在 6 个尸体标本的滑车(20、25 和 30mm)和 MFC(15、20 和 25mm)上制作缺损。使用 2 种不同的技术应用移植物:(1)突出,纤维蛋白水平超出周围软骨;(2)凹陷,纤维蛋白水平与周围软骨平齐或低于周围软骨。通过使用连续被动运动机器在运动范围内对膝关节进行循环。评估缺损处的浅层分层和移植物的位移。这被量化为表面分层和/或暴露骨的百分比。比较了缺损大小、位置和填充。
在 MFC 和滑车中,突出应用导致纤维蛋白分层的发生率增加。在滑车中,与凹陷的 20mm 缺损相比,突出的 30mm 缺损中检测到平均 38%的分层(P<.05)。这种效应随着缺损尺寸的增加而增加。在 MFC 中,与 25mm 处的 95%分层和 71%暴露骨相比,在突出的 15mm 缺损中注意到 43%和 28%暴露骨的平均分层。在 82%的标本中,在测试的前 15 分钟内发生了移植物和/或分层。
滑车和股骨髁的缺损尺寸增加以及突出的构建应用与移植物/纤维蛋白构建物的明显分层和位移有关。
在滑车和 MFC 缺损中,突出应用移植物增加了纤维蛋白分层和移植物移位的可能性。这种效应随着缺损尺寸的增加而增加。这些数据可能支持限制移植物手术后的活动范围。