Jeffrey A. Feinstein, MD, MPH

Publication Details

  • Computational Simulations for Aortic Coarctation: Representative Results From a Sampling of Patients JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME LaDisa, J. F., Figueroa, C. A., Vignon-Clementel, I. E., Kim, H. J., Xiao, N., Ellwein, L. M., Chan, F. P., Feinstein, J. A., Taylor, C. A. 2011; 133 (9)


    Treatments for coarctation of the aorta (CoA) can alleviate blood pressure (BP) gradients (?), but long-term morbidity still exists that can be explained by altered indices of hemodynamics and biomechanics. We introduce a technique to increase our understanding of these indices for CoA under resting and nonresting conditions, quantify their contribution to morbidity, and evaluate treatment options. Patient-specific computational fluid dynamics (CFD) models were created from imaging and BP data for one normal and four CoA patients (moderate native CoA: ?12 mmHg, severe native CoA: ?25 mmHg and postoperative end-to-end and end-to-side patients: ?0 mmHg). Simulations incorporated vessel deformation, downstream vascular resistance and compliance. Indices including cyclic strain, time-averaged wall shear stress (TAWSS), and oscillatory shear index (OSI) were quantified. Simulations replicated resting BP and blood flow data. BP during simulated exercise for the normal patient matched reported values. Greatest exercise-induced increases in systolic BP and mean and peak ?BP occurred for the moderate native CoA patient (SBP: 115 to 154 mmHg; mean and peak ?BP: 31 and 73 mmHg). Cyclic strain was elevated proximal to the coarctation for native CoA patients, but reduced throughout the aorta after treatment. A greater percentage of vessels was exposed to subnormal TAWSS or elevated OSI for CoA patients. Local patterns of these indices reported to correlate with atherosclerosis in normal patients were accentuated by CoA. These results apply CFD to a range of CoA patients for the first time and provide the foundation for future progress in this area.

    View details for DOI 10.1115/1.4004996

    View details for Web of Science ID 000295882200008

    View details for PubMedID 22010743

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