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. 2020 May;48(5):1475-1490.
doi: 10.1007/s10439-020-02466-4. Epub 2020 Feb 7.

Fluid-Structure Interaction Models of Bioprosthetic Heart Valve Dynamics in an Experimental Pulse Duplicator

Affiliations

Fluid-Structure Interaction Models of Bioprosthetic Heart Valve Dynamics in an Experimental Pulse Duplicator

Jae H Lee et al. Ann Biomed Eng. 2020 May.

Abstract

Computer modeling and simulation is a powerful tool for assessing the performance of medical devices such as bioprosthetic heart valves (BHVs) that promises to accelerate device design and regulation. This study describes work to develop dynamic computer models of BHVs in the aortic test section of an experimental pulse-duplicator platform that is used in academia, industry, and regulatory agencies to assess BHV performance. These computational models are based on a hyperelastic finite element extension of the immersed boundary method for fluid-structure interaction (FSI). We focus on porcine tissue and bovine pericardial BHVs, which are commonly used in surgical valve replacement. We compare our numerical simulations to experimental data from two similar pulse duplicators, including a commercial ViVitro system and a custom platform related to the ViVitro pulse duplicator. Excellent agreement is demonstrated between the computational and experimental results for bulk flow rates, pressures, valve open areas, and the timing of valve opening and closure in conditions commonly used to assess BHV performance. In addition, reasonable agreement is demonstrated for quantitative measures of leaflet kinematics under these same conditions. This work represents a step towards the experimental validation of this FSI modeling platform for evaluating BHVs.

Keywords: Bovine pericardial valve; Finite element method; Immersed boundary method; Porcine aortic valve.

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Figures

Figure 1
Figure 1
(a) A customized pulse duplicator based on the commercial ViVitro pulse-duplicator system adapted with prototype electro-optical subsystem for measuring aortic valve projected dynamic valve area (PDVA), or alternate configuration for measuring mitral valve PDVA. (b) A schematic diagram of the custom pulse duplicator based on the commercial ViVitro pulse-duplicator system adapted with prototype electro-optical subsystem for measuring aortic valve PDVA or alternate configuration for measuring mitral valve PDVA. The commercial ViVitro system is similar but lacks the back light and the photo sensor for acquiring PDVA.
Figure 2
Figure 2
(a) Model porcine bioprosthetic valve geometry and fiber architecture. The idealized geometry of the Labcor TLBP A Supra porcine aortic valve is reconstructed based on literature values. The model fiber structure is generated using Poisson interpolation. (b) Model bovine pericardial bioprosthetic valve geometry and fiber architecture. This valve geometry is obtained from micro-CT imaging of a Carpentier–Edwards PERIMOUNT RSR Model 2800 surgical aortic heart valve. The model fiber structure is generated based on the small angle light scattering (SALS) data of Sun et al. The SALS data show that the mean fiber orientation of a bovine pericardial valve leaflet is 45.
Figure 3
Figure 3
Three-dimensional aortic test section models for the porcine (a) and bovine pericardial (b) BHV simulations along with the reduced-order models that provide driving and loading conditions. Three-element Windkessel models are used at the downstream (outlet) for both cases. (a) A three-element Windkessel model is used at the upstream (inlet) for the porcine aortic valve simulations. The pump pressure is derived from pressure and flow data from the ventricular outflow tract of the pulse duplicator. (b) Because the pump flow waveform and atrial pressure are available for the bovine pericardial valve experiments, a more detailed pump model is used upstream for the bovine pericardial valve simulations.
Figure 4
Figure 4
Comparisons between simulated and experimental pressure and flow rate waveforms for the porcine aortic valve (a, b) and bovine pericardial valve (c, d). The experimental waveforms shown are the average waveforms over 10 consecutive cycles of data, with shaded regions showing where 95% of the data fall. The experimental and computational stroke volumes for the porcine aortic valve are 69.4±0.4 and 72.7mL, respectively, and 71.6±0.7 and 72.1mL for the bovine pericardial valve. The maximum experimental pressure differences during forward flow for the porcine aortic and bovine pericardial valves are 22.8±0.2 and 19.7±0.5mmHg, respectively. The maximum computational pressure differences during forward flow are 22.4 and 16.4mmHg, respectively.
Figure 5
Figure 5
Comparisons between simulated and experimental projected dynamic valve area (PDVA) for the porcine aortic (a) and bovine pericardial (b) valves. (a) The experimental data (acquired using the custom apparatus depicted in Fig. 1b) are manually aligned with the beginning of the valve opening with the simulation data. The experimental PDVA measurement shown is the average PDVA over 10 consecutive cycles of data with shaded region showing where 95% of the data fall. (b) The experimental data are acquired using a high-speed videographic method, from which we reconstruct PDVA data using automatic image analysis using DataTank. Videographic data are available for only a single cycle for the pericardial BHV.
Figure 6
Figure 6
Detailed comparison of the bovine pericardial valve leaflet kinematics during closure in the simulation (top) and experiment (bottom). The simulation captures the behavior of each of the leaflets closing one at a time (order: bottom right left leaflet) as observed in the experiment. The time increment between frames for simulation is 9.6 ms.
Figure 7
Figure 7
Cross-section view of simulated flow patterns using the porcine aortic (a) and bovine pericardial (b) valve models. The color shows the axial velocity through the aortic test section at the center plane, with red indicating forward flow and blue indicating reverse flow. (a) Repeak=20,576. (b) Repeak=19,330. The time increment between frames is 57.6 ms.
Figure 8
Figure 8
Leaflet kinematics of the porcine aortic (a) and bovine pericardial (b) valves during opening. (a) The time increment between frames is 1.92 ms. (b) The time increment between frames is 3.84 ms.
Figure 9
Figure 9
Leaflet kinematics of the porcine aortic (a) and bovine pericardial (b) valves during closure. (a) The time increment between frames is 9.6 ms. (b) The time increment between frames is 19.2 ms.
Figure 10
Figure 10
von Mises stress (kPa) on the porcine aortic (a, c) and bovine pericardial (b, d) valves during diastole (a, b) and systole (c, d). The time increment between frames in panels (a, b) is 30.72 ms, and the time increment between frames in panels (c, d) is 11.52 ms.

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