TY - JOUR
T1 - Autogenous flexor-tendon grafts. A biomechanical and morphological study in dogs
AU - Seiler, J. G.
AU - Gelberman, R. H.
AU - Williams, C. S.
AU - Woo, S. L.Y.
AU - Dickersin, G. R.
AU - Sofranko, R.
AU - Chu, C. R.
AU - Rosenberg, A. E.
PY - 1993
Y1 - 1993
N2 - Intrasynovial and extrasynovial donor autogenous flexor-tendon grafts were placed in the synovial sheaths of the medial and lateral digits of the forepaw in twenty dogs (forty tendons). Postoperatively, the dogs were managed with early, controlled, passive mobilization. Histological and ultrastructural evaluations were carried out at ten days, three weeks, and six weeks, and biomechanical analyses were performed at three and six weeks. The intrasynovial and extrasynovial tendon grafts showed different healing processes histologically. The extrasynovial tendon grafts healed with early ingrowth of peripheral adhesions, which appeared to become larger and more dense over time. These grafts exhibited decreased cellularity and early neovascularization at ten days, and there was evidence of progressive revascularization and cellular repopulation at three and six weeks. In contrast, the intrasynovial tendon grafts demonstrated minimum adhesions, and both cellularity and collagen organization were normal at each time-interval. The intrasynovial grafts had significantly more angular rotation at the proximal interphalangeal joint at three and six weeks than did the extrasynovial grafts (p < 0.05). CLINICAL RELEVANCE: The intrasynovial donor tendon grafts had significantly improved morphological and functional characteristics compared with the extrasynovial tendon grafts at each interval of assessment (p < 0.05). These data provide the basis for an explanation of the variable results seen clinically when extrasynovial donor tendons have been used as autogenous grafts in the hand; they also support the concept that intrasynovial tendons may be especially suitable for survival in the environment of the digital sheath.
AB - Intrasynovial and extrasynovial donor autogenous flexor-tendon grafts were placed in the synovial sheaths of the medial and lateral digits of the forepaw in twenty dogs (forty tendons). Postoperatively, the dogs were managed with early, controlled, passive mobilization. Histological and ultrastructural evaluations were carried out at ten days, three weeks, and six weeks, and biomechanical analyses were performed at three and six weeks. The intrasynovial and extrasynovial tendon grafts showed different healing processes histologically. The extrasynovial tendon grafts healed with early ingrowth of peripheral adhesions, which appeared to become larger and more dense over time. These grafts exhibited decreased cellularity and early neovascularization at ten days, and there was evidence of progressive revascularization and cellular repopulation at three and six weeks. In contrast, the intrasynovial tendon grafts demonstrated minimum adhesions, and both cellularity and collagen organization were normal at each time-interval. The intrasynovial grafts had significantly more angular rotation at the proximal interphalangeal joint at three and six weeks than did the extrasynovial grafts (p < 0.05). CLINICAL RELEVANCE: The intrasynovial donor tendon grafts had significantly improved morphological and functional characteristics compared with the extrasynovial tendon grafts at each interval of assessment (p < 0.05). These data provide the basis for an explanation of the variable results seen clinically when extrasynovial donor tendons have been used as autogenous grafts in the hand; they also support the concept that intrasynovial tendons may be especially suitable for survival in the environment of the digital sheath.
UR - http://www.scopus.com/inward/record.url?scp=0027301352&partnerID=8YFLogxK
U2 - 10.2106/00004623-199307000-00006
DO - 10.2106/00004623-199307000-00006
M3 - Article
C2 - 8335659
AN - SCOPUS:0027301352
SN - 0021-9355
VL - 75
SP - 1004
EP - 1014
JO - Journal of Bone and Joint Surgery - Series A
JF - Journal of Bone and Joint Surgery - Series A
IS - 7
ER -