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Clin Orthop Relat Res. 2011 Oct;469(10):2831-7. doi: 10.1007/s11999-011-1893-z. Epub 2011 Apr 30.

Vascularized bone grafting in a canine carpal avascular necrosis model.

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1
Department of Orthopedics, Orthopedic Research, Microvascular Research Laboratory, Mayo Clinic, 200 First Street, SW, Rochester, MN 55905, USA.

Abstract

BACKGROUND:

Limited experimental research has been performed on the treatment of avascular necrosis (AVN) by vascularized bone grafting.

QUESTIONS/PURPOSES:

A new model simulating carpal AVN was created to investigate surgical revascularization of necrotic bone.

METHODS:

In seven mongrel dogs, AVN was induced by removal of the radial carpal bones bilaterally, deep-freezing, coating in cyanoacrylate, and reimplantation. A reverse-flow vascularized bone graft from the distal radius was implanted in the avascular radial carpal bone. The contralateral side served as an untreated ischemic control. Bone blood flow, bone volume, radiography, histomorphometry, histology, and MRI were analyzed at 4 weeks.

RESULTS:

Blood flow was substantially higher in grafted bones when compared with controls (14.68 ± 15.43 versus 0.27 ± 0.28 mL/minute/100 g). Blood flow correlated with increased osteoid formation and higher levels of bone turnover. T1 and T2 signals on MRI did not correlate with quantitative bone blood flow measurements. Necrotic bones with no blood flow had normal T1 and T2 signals, whereas revascularized bones had signal changes when compared with adjacent carpal bones. No major collapse occurred in any radiocarpal bone.

CONCLUSION:

In a canine experimental model, investigation of carpal AVN shows the ability of vascularized bone grafting to revascularize and remodel avascular bone.

CLINICAL RELEVANCE:

Surgical revascularization of necrotic bone induced by vascularized bone grafting results in increased bone perfusion and bone remodeling as compared with untreated necrotic bone. MRI T1 and T2 signals can be normal in necrotic avascular bone.

PMID:
21533527
PMCID:
PMC3171535
DOI:
10.1007/s11999-011-1893-z
[Indexed for MEDLINE]
Free PMC Article
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