Title | A comparison of patellar tendon autograft and allograft used for anterior cruciate ligament reconstruction in the goat model |
Publication Type | Journal Article |
Year of Publication | 1993 |
Authors | Jackson DW, Grood ES, Goldstein JD, Rosen MA, Kurzweil PR, Cummings JF, Simon TM |
Journal | Am J Sports Med |
Volume | 21 |
Issue | 2 |
Pagination | 176 - 85 |
Date Published | Mar-Apr |
ISSN | 0363-5465 (Print) 0363-5465 (Linking) |
Accession Number | 8465909 |
Keywords | Animals, Anterior Cruciate Ligament / *injuries / *surgery, Collagen, Female, Goats, Hindlimb / surgery, Microscopy, Electron, Tendons / pathology / *transplantation, Time Factors, Transplantation, Autologous, Transplantation, Homologous |
Abstract | Similar-sized patellar tendon autografts and fresh-frozen allografts were used to reconstruct the anterior cruciate ligament of one knee in 40 female goats. Evaluations of the reconstructions and contralateral controls at the 6-week and 6-month postoperative periods included anterior-posterior translation, mechanical properties determined during tensile failure tests, measurement of cross-sectional area, histology, collagen fibril size and area distribution, and associated articular cartilage degenerative changes. Six months after anterior cruciate ligament reconstruction, the autografts demonstrated a smaller increase in anterior-posterior displacement, values of maximum force to failure two times greater, a significant increase in cross-sectional area, a more rapid loss of large-diameter collagen fibrils, and an increased density and number of small-diameter collagen fibrils compared to the allografts. Clinical significance. More surgeons are allowing their patients to return to running and sports 6 months after anterior cruciate ligament reconstruction. While the structural and material properties of autografts and allografts at time zero are similar, in the goat model during the first 6 months they differ. The allografts demonstrate a greater decrease in their implantation structural properties, a slower rate of biologic incorporation, and the prolonged presence of an inflammatory response. At 6 months the autograft demonstrates a more robust biologic response, improved stability, and increased strength to failure values. |
Notify Library Reference ID | 729 |