Key result
A patient-specific multi-scale computational model successfully predicted the locations of critical neointimal hyperplasia development in two vein grafts, showing agreement with clinical data.
A novel patient-specific computational framework combining biochemical and fluid dynamics models shows potential in predicting locations of neointimal hyperplasia in vein grafts.
Offers an early proof-of-concept tool for predicting graft failure that should not yet change practice;.
Neointimal hyperplasia is amongst the major causes of failure of bypass grafts. The disease progression varies from patient to patient due to a range of different factors. In this paper, a mathematical model will be used to understand neointimal hyperplasia in individual patients, combining information from biological experiments and patient-specific data to analyze some aspects of the disease, particularly with regard to mechanical stimuli due to shear stresses on the vessel wall. By combining a biochemical model of cell growth and a patient-specific computational fluid dynamics analysis of blood flow in the lumen, remodeling of the blood vessel is studied by means of a novel computational framework. The framework was used to analyze two vein graft bypasses from one patient: a femoro-popliteal and a femoro-distal bypass. The remodeling of the vessel wall and analysis of the flow for each case was then compared to clinical data and discussed as a potential tool for a better understanding of the disease. Simulation results from this first computational approach showed an overall agreement on the locations of hyperplasia in these patients and demonstrated the potential of using new integrative modeling tools to understand disease progression.
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Donadoni et al. (2017) studied Neointimal hyperplasia in vein grafts (n=1). Patient-specific multi-scale computational modeling vs. Clinical CT scan data was evaluated on Location and extent of neointimal hyperplasia. A patient-specific multi-scale computational model successfully predicted the locations of critical neointimal hyperplasia development in two vein grafts, showing agreement with clinical data.
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