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This study reports the first use of ultrasound (US) elastography for imaging spinal fractures by assessing the mechanical response of the soft tissue at the posterior vertebra boundary to a uniaxial compression in rabbit ex vivo samples. Three-dimensional finite-element (FE) models of the vertebra-soft tissue complex in rabbit samples are generated and analyzed to evaluate the distribution of the axial normal and shear strains at the vertebra-soft tissue interface. Experiments on the same samples are performed to corroborate simulation findings. Results of this study indicate that the distribution of the axial strains manifests as distinct patterns around intact and fractured vertebrae. Numerical characteristics of the axial strain’s spatial distribution are further used to construct two shape descriptors to make inferences on spinal abnormalities: 1) axial normal strain asymmetry for assessing the presence of fractures and 2) principal orientation of axial shear strain concentration regions (shear zones) for measurement of spinous process dislocation. This study demonstrates that axial normal strain and axial shear strain maps obtained via US elastography can provide a new means to detect spine fractures and abnormalities in the selected ex vivo animal models. Spinal fracture detection is important for the assessment of spinal cord injuries and stability. However, identification of spinal fractures using US is currently challenging. Our results show that features resulting from strain elastograms can serve as a useful adjunct to B-mode images in identifying spine fractures in the selected animal samples, and this information could be helpful in clinical settings. [ABSTRACT FROM AUTHOR]

The mechanical behavior of long bones and fractures has been under investigation for many decades due to its complexity and clinical relevance. In this paper, we report a new subject-specific methodology to predict and analyze the mechanical behavior of the soft tissue at a bone interface with the intent of identifying the presence and location of bone abnormalities with high accuracy, spatial resolution, and contrast. The proposed methodology was tested on both intact and fractured rabbit femur samples with finite element-based 3-D simulations, created from actual femur computed tomography data, and ultrasound elastography experiments. The results included in this study demonstrate that elastographic strains at the bone/soft tissue interface can be used to differentiate fractured femurs from the intact ones on a distribution level. These results also demonstrate that coronal plane axial shear strain creates a unique contrast mechanism that can be used to reliably detect fractures (both complete and incomplete) in long bones. Kruskal–Wallis test further demonstrates that the contrast measure for the fracture group (simulation: 2.1286±0.2206; experiment: 2.7034 ± 1.0672) is significantly different from that for the intact group (simulation: 0 ± 0; experiment: 1.1540±0.6909) when using coronal plane axial shear strain elastography ($p$ < 0.01). We conclude that: 1) elastography techniques can be used to accurately identify the presence and location of fractures in a long bone and 2) the proposed model-based approach can be used to predict and analyze strains at a bone fracture site and to better interpret experimental elastographic data. [ABSTRACT FROM AUTHOR]