When developing high-fidelity computational model of vocal fold vibration for voice production of individuals, one would run into typical issues of unknown model parameters and model validation of individual-specific characteristics of phonation. In the current study, the evoked rabbit phonation is adopted to explore some of these issues. In particular, the mechanical properties of the rabbit's vocal fold tissue are unknown for individual subjects. In the model, we couple a 3D vocal fold model that is based on the magnetic resonance (MR) scan of the rabbit larynx and a simple one-dimensional (1D) model for the glottal airflow to perform fast simulations of the vocal fold dynamics. This hybrid three-dimensional (3D)/1D model is then used along with the experimental measurement of each individual subject for determination of the vocal fold properties. The vibration frequency and deformation amplitude from the final model are matched reasonably well for individual subjects. The modeling and validation approaches adopted here could be useful for future development of subject-specific computational models of vocal fold vibration.
We present a novel reduced-order glottal airflow model that can be coupled with the three-dimensional (3D) solid mechanics model of the vocal fold tissue to simulate the fluid–structure interaction (FSI) during voice production. This type of hybrid FSI models have potential applications in the estimation of the tissue properties that are unknown due to patient variations and/or neuromuscular activities. In this work, the flow is simplified to a one-dimensional (1D) momentum equation-based model incorporating the entrance effect and energy loss in the glottis. The performance of the flow model is assessed using a simplified yet 3D vocal fold configuration. We use the immersed-boundary method-based 3D FSI simulation as a benchmark to evaluate the momentum-based model as well as the Bernoulli-based 1D flow models. The results show that the new model has significantly better performance than the Bernoulli models in terms of prediction about the vocal fold vibration frequency, amplitude, and phase delay. Furthermore, the comparison results are consistent for different medial thicknesses of the vocal fold, subglottal pressures, and tissue material behaviors, indicating that the new model has better robustness than previous reduced-order models.
Objectives/Hypothesis
Vocal fold scar is a major cause of dysphonia, and optimal treatments do not currently exist. Small intestinal submucosa (SIS) is a biomaterial developed for the treatment of a variety of pathologies. The purpose of this study was to investigate the effects of SIS implantation on tissue remodeling in scarred vocal folds using routine staining, immunohistochemistry, and high‐speed videoendoscopy (HSV).
Study Design
Prospective, blinded group analysis.
Methods
Thirteen New Zealand White rabbits underwent a vocal fold scarring procedure followed by microflap elevation with or without SIS implantation. Seven months later, they underwent a phonation procedure with HSV and laryngeal harvest. Alcian blue and elastica van Gieson staining and immunohistochemistry for collagen types I and III were used to evaluate histological healing outcomes. Dynamic functional remodeling of the scarred vocal fold in the presence of SIS implants was evaluated using HSV imaging to capture restoration of vibratory amplitude, amplitude ratio, and left‐right phase symmetry.
Results
Density of collagen I was significantly decreased in SIS versus microflap‐treated vocal folds. No differences were found between groups for hyaluronic acid, elastin, or collagen type III. Organization of elastin in the subepithelial region appeared to affect amplitude of vibration and the shape of the vocal fold edge.
Conclusions
SIS implantation into chronic scar reduced the density of collagen I deposits. There was no evidence of a negative impact or complication from SIS implantation. Regardless of treatment type, organization of elastin in the subepithelial region may be important to vibratory outcomes.
Level of Evidence
NA. Laryngoscope, 128:901–908, 2018
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