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DOI 10.1016/j.medengphy.2009.06.010

Медицинская библиотека · Medical engineering & physics · 2009

A fracture risk assessment model of the femur in children with osteogenesis imperfecta (OI) during gait.

Fritz Jessica M, Guan Yabo, Wang Mei, Smith Peter A, Harris Gerald F

СтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

Osteogenesis imperfecta (OI) is a heritable bone fragility disorder characterized by skeletal deformities and increased bone fragility. There is currently no established clinical method for quantifying fracture risk in OI patients. This study begins the development of a patient-specific model for femur fracture risk assessment and prediction based on individuals' gait analysis data, bone geometry from imaging and material properties from nanoindentation (Young's modulus=19 GPa, Poisson's ratio=0.3). Finite element models of the femur were developed to assess fracture risk of the femur in a pediatric patient with OI type I. Kinetic data from clinical gait analysis was used to prescribe loading conditions on the femoral head and condyles along with muscle forces on the bone's surface. von Mises stresses were analyzed against a fracture strength of 115 MPa. The patient with OI whose femur was modeled showed no risk of femoral fracture during normal gait. The highest stress levels occurred during the mid-stance and loading responses phases of gait. The location of high stress migrated throughout the femoral diaphysis across the gait cycle. Maximum femoral stress levels occurred during the gait cycle phases associated with the highest loading. The fracture risk (fracture strength/von Mises stress), however, was low. This study provides a relevant method for combining functional activity, material property and analytical methods to improve patient monitoring.

Для цитирования: Fritz Jessica M, Guan Yabo, Wang Mei, Smith Peter A, Harris Gerald F. A fracture risk assessment model of the femur in children with osteogenesis imperfecta (OI) during gait.. Medical engineering & physics. 2009. DOI: 10.1016/j.medengphy.2009.06.010.

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