The most popular replacement heart valve designs (so called ?bioprosthetic heart valves? or BHV) continue to be fabricated from xenograft biomaterials for both current and novel valve designs (e.g. standard stented valve, percutaneous delivery). Failure continues to be the result of leaflet structural deterioration mediated by fatigue and/or tissue mineralization, with durability limited to 10-15 years. Such limitations results from a combination of valve design and the intrinsic fatigue response of the constituent xenograft biomaterials. Thus, improved durability remains an important clinical goal and represents a unique cardiovascular engineering challenge resulting from the extreme valvular mechanical demands that occur with blood contact. Yet, current BHV assessment relies exclusively on device-level evaluations, which are confounded by simultaneous and highly coupled biomaterial mechanical behaviors and fatigue, valve design, hemodynamics, and calcification. Thus, despite decades of clinical BHV usage and growing popularity, there exists no acceptable method for simulating replacement valve function and durability at both the device and component biomaterial levels. This situation has contributed to the current stagnation in BHV development, limiting rationally developed improvements in prosthetic heart valve durability. We thus hypothesize that with the use of advanced biosolid mechanics simulations of the fatigue response of xenograft biomaterials coupled to state-of-the-art fluid-structure interaction (FSI) methods, a biomechanically rigorous and physiologically realistic approach to predict BHV performance can be developed. We will develop these coupled computational goals first in parallel, then combine and validate them in a final project stage.

Public Health Relevance

The most popular replacement heart valve designs (so called ?bioprosthetic heart valves? or BHV) continue to fail as a result of leaflet structural with durability limited to 10-15 years. We plan to use of advanced biosolid mechanics simulations to develop a biomechanically rigorous and physiologically realistic approach to predict BHV performance as a tool for BHV designs.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL129077-02
Application #
9275533
Study Section
Modeling and Analysis of Biological Systems Study Section (MABS)
Program Officer
Evans, Frank
Project Start
2016-05-19
Project End
2020-04-30
Budget Start
2017-05-01
Budget End
2018-04-30
Support Year
2
Fiscal Year
2017
Total Cost
$562,971
Indirect Cost
$100,172
Name
University of Texas Austin
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
170230239
City
Austin
State
TX
Country
United States
Zip Code
78712
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Zhang, Will; Sacks, Michael S (2017) Modeling the response of exogenously crosslinked tissue to cyclic loading: The effects of permanent set. J Mech Behav Biomed Mater 75:336-350
Wang, Chenglong; Xu, Fei; Hsu, Ming-Chen et al. (2017) Rapid B-rep model preprocessing for immersogeometric analysis using analytic surfaces. Comput Aided Geom Des 52-53:190-204
Kamensky, David; Hsu, Ming-Chen; Yu, Yue et al. (2017) Immersogeometric cardiovascular fluid-structure interaction analysis with divergence-conforming B-splines. Comput Methods Appl Mech Eng 314:408-472
Kamensky, David; Evans, John A; Hsu, Ming-Chen et al. (2017) Projection-based stabilization of interface Lagrange multipliers in immersogeometric fluid-thin structure interaction analysis, with application to heart valve modeling. Comput Math Appl 74:2068-2088

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