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Coagulopathy
Study
Osteonecrosis
has been shown to be associated with systemic lupus erythematosus,
sickle cell disease, Gaucher disease, corticosteroids, and alcohol
use. What triggers the disease in a small percentage of individuals
with these factors and/or diseases is not known. Furthermore,
there is a group of patients where no obvious underlying factors
have been identified. As recent reports in the medical literature
have provided evidence that patients with osteonecrosis may
have defects in their blood clotting system, we currently screen
all of our osteonecrosis patients for coagulopathies. An initial
review of the laboratory test results revealed that 22 of 26
(83%) of the patients with osteonecrosis had a coagulation abnormality.
Although coagulopathies are also detected in the normal population,
the frequency of these abnormalities is noticeably higher in
patients with osteonecrosis. Larger numbers of patients and
matched control subjects are needed to define the association
between coagulopathies and osteonecrosis.
Animal Models
In many musculoskeletal diseases, animal
models have been used to study the pathogenesis, i.e., the development,
of the disease process as well as to study the effectiveness
of different approaches to treatment. The investigation of the
pathogenesis of osteonecrosis is hindered by the lack of an
adequate animal model.
In 1996, Michael A. Mont, M.D. received a 2-year grant from the
Orthopaedic Research and Education Foundation to study an animal
model. This grant was entitled Femoral Head Collapse: Prevention
with Strut Autografting With or Without Bone Morphogenetic Proteins.
This model simulates the circumstances associated with one type
of treatment for osteonecrosis, the "Trapdoor" procedure.
In this procedure, diseased bone is removed through a trapdoor in
the cartilage. The bone is then replaced with bone graft or a bone
graft substitute. This study seeks not only to further characterize
this model, but also to evaluate the use of bone graft with bone
morphogenetic protein, a protein shown to stimulate bone formation.
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