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Clin. Orthop. Relat. Res. · May 2013
Heterotopic bone formation about the hip undergoes endochondral ossification: a rabbit model.
- Oliver Tannous, Alec C Stall, Cullen Griffith, Christopher T Donaldson, Rudolph J Castellani, and Vincent D Pellegrini.
- Department of Orthopaedics, University of Maryland School of Medicine, 22 South Green Street, Suite S-11B, Baltimore, MD, USA.
- Clin. Orthop. Relat. Res. 2013 May 1; 471 (5): 1584-92.
BackgroundHeterotopic ossification (HO) occurs most commonly after trauma and surgery about the hip and may compromise subsequent function. Currently available animal models describing the cellular progression of HO are based on exogenous osteogenic induction agents and may not reflect the processes following trauma.Questions/PurposesWe therefore sought to characterize the histologic progression of heterotopic bone formation in an animal model that recapitulates the human condition without the addition of exogenous osteogenic material.MethodsWe used a rabbit model that included intramedullary instrumentation of the upper femur and ischemic crush injury of the gluteal muscle. Bilateral surgical induction procedures were performed on 30 animals with the intention of inciting the process of HO; no supplemental osteogenic stimulants were used. Three animals were sacrificed at each of 10 predetermined times between 1 day and 26 weeks postoperatively and the progression of tissue maturation was graded histologically using a five-item scale.ResultsHeterotopic bone reliably formed de novo and consistently followed a pathway of endochondral ossification. Chondroid elements were found in juxtaposition with immature woven bone in all sections that contained mature osseous elements.ConclusionsThese results establish that HO occurs in an animal model mimicking the human condition following surgical trauma about the hip; it is predictable in its histologic progression and follows a pathway of endochondral bone formation.Clinical RelevanceBy showing a consistent pathway of endochondral ossification leading to ectopic bone formation, this study provides a basis for understanding the mechanisms by which HO might be mitigated by interventions.
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