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1.
Phys Med Biol ; 63(20): 205011, 2018 10 17.
Article in English | MEDLINE | ID: mdl-30247153

ABSTRACT

Before embarking on a series of in vivo tests, design of ultrasound-flow-imaging modalities are generally more efficient through computational models as multiple configurations can be tested methodically. To that end, simulation models must generate realistic blood flow dynamics and Doppler signals. The current in silico ultrasound simulation techniques suffer mainly from uncertainty in providing accurate trajectories of moving ultrasound scatterers. In mesh-based Eulerian methods, numerical truncation errors from the interpolated velocities, both in the time and space dimensions, can accumulate significantly and make the pathlines unreliable. These errors can distort beam-to-beam inter-correlation present in ultrasound flow imaging. It is thus a technical issue to model a correct motion of the scatterers by considering their interaction with boundaries and neighboring scatterers. We hypothesized that in silico analysis of emerging ultrasonic imaging modalities can be implemented more accurately with meshfree approaches. We developed an original fluid-ultrasound simulation environment based on a meshfree Lagrangian CFD (computational fluid dynamics) formulation, which allows analysis of ultrasound flow imaging. This simulator combines smoothed particle hydrodynamics (SPH) and Fourier-domain linear acoustics (SIMUS = simulator for ultrasound imaging). With such a particle-based computation, the fluid particles also acted as individual ultrasound scatterers, resulting in a direct and physically sound fluid-ultrasonic coupling. We used the in-house algorithms for fluid and ultrasound simulations to simulate high-frame-rate vector flow imaging. The potential of the particle-based method was tested in 2D simulations of vector Doppler for the intracarotid flow. The Doppler-based velocity fields were compared with those issued from SPH. The numerical evaluations showed that the vector flow fields obtained by vector Doppler components were in good agreement with the original SPH velocities, with relative errors less than 10% and 2% in the cross-beam and axial directions, respectively. Our results showed that SPH-SIMUS coupling enables direct and realistic simulations of ultrasound flow imaging. The proposed coupled algorithm has also the advantage to be 3D compatible and parallelizable.


Subject(s)
Computer Simulation , Hydrodynamics , Algorithms , Hemodynamics , Humans , Image Processing, Computer-Assisted , Models, Cardiovascular , Ultrasonography
2.
Artif Organs ; 42(5): 516-524, 2018 May.
Article in English | MEDLINE | ID: mdl-29168199

ABSTRACT

Mitral valve percutaneous edge-to-edge repair (PEtER) is a viable solution in high-risk patients with severe symptomatic mitral regurgitation. However, the generated double-orifice configuration poses challenges for the evaluation of the hemodynamic performance of the mitral valve and may alter flow patterns in the left ventricle (LV) during diastole. This in vitro study aims to evaluate the hemodynamic modifications following a simulated PEtER. A custom-made mitral valve was developed, and two configurations were tested: (i) a single-orifice valve with mitral regurgitation and (ii) a double-orifice mitral valve configuration following PEtER. The hemodynamic performance of the valve was evaluated using Doppler echocardiography and catheterization, while the flow patterns in the LV were investigated using particle image velocimetry (PIV). The tests were run at a stroke volume of 65 mL and a heart rate of 70 bpm. PEtER was found to significantly reduce the regurgitant volume (15 vs. 34 mL). There was a good agreement between Doppler and catheter transmitral pressure gradients (peak gradient: 9 vs. 7 mm Hg; mean gradient: 4 vs. 3 mm Hg) as well as an excellent agreement between maximal velocity measured by Doppler and PIV (1.60 vs. 1.58 m/s). Vortex development in the LV during diastole was significantly different after repair. PEtER significantly increased the amplitude of Reynolds and viscous shear stresses, as well as the number of high shear regions in the LV, potentially promoting thromboembolism events.


Subject(s)
Heart Ventricles/physiopathology , Mitral Valve Insufficiency/surgery , Mitral Valve/surgery , Cardiac Valve Annuloplasty/instrumentation , Echocardiography, Doppler , Equipment Design , Heart Valve Prosthesis , Heart Ventricles/diagnostic imaging , Hemodynamics , Humans , Mitral Valve/diagnostic imaging , Mitral Valve/physiopathology , Mitral Valve Insufficiency/diagnostic imaging , Mitral Valve Insufficiency/physiopathology , Models, Cardiovascular , Rheology
3.
Can J Cardiol ; 31(8): 1041-6, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26211709

ABSTRACT

BACKGROUND: There are few data about the patient- and prosthesis-related factors influencing the hemodynamics of transcatheter heart valves (THVs). The objective of this in vitro study was to assess the effect of aortic annulus size and prosthesis oversizing on the valve hemodynamics and estimated leaflet bending stress of the Edwards SAPIEN balloon-expandable THV (Edwards Lifesciences, Irvine, CA). METHODS: The effective orifice area (EOA) of the 23-mm and 26-mm SAPIEN THVs were measured by Doppler echocardiography in a pulse duplicator under the following experimental conditions: (1) stroke volume of 20, 30, 50, 70, and 80 mL and (2) aortic annulus size of 19, 20, 21, and 22 mm for the 23-mm SAPIEN and 22, 23, and 24, and 25 mm for the 26-mm SAPIEN. The percentage of valve oversizing was calculated as follows: % OS = 100 × [(prosthesis nominal area - aortic annulus area)/aortic annulus area], where % OS is the percentage of oversizing. The leaflet bending stress was measured by high-speed camera imaging of the THV leaflet opening. RESULTS: The 2 independent determinants of valve EOA were the aortic annulus diameter (R(2) = 0.33; P < 0.001) and the stroke volume (R(2) = 0.63; P < 0.001). The prosthesis size and % OS were not independently related to EOA. However, a larger % OS was independently associated with higher peak systolic leaflet bending stress (ΔR(2) = 0.11; P < 0.0001). CONCLUSIONS: The hemodynamic performance of THV is in large part determined by the aortic annulus diameter in which the valve is deployed. Oversizing (up to 20% in area) has no significant effect on valve EOA but is associated with higher leaflet bending stress, which might promote faster structural valve degeneration in the long term.


Subject(s)
Aortic Valve Stenosis/surgery , Aortic Valve/diagnostic imaging , Heart Valve Prosthesis , Hemodynamics , Models, Biological , Transcatheter Aortic Valve Replacement , Aortic Valve/surgery , Aortic Valve Stenosis/diagnostic imaging , Aortic Valve Stenosis/physiopathology , Echocardiography, Doppler , Humans , Prosthesis Design
4.
J Biomech Eng ; 136(5): 054501, 2014 May.
Article in English | MEDLINE | ID: mdl-24474441

ABSTRACT

A significant number of elderly patients with severe symptomatic aortic stenosis are denied surgical aortic valve replacement (SAVR) because of high operative risk. Transcatheter aortic valve implantation (TAVI) has emerged as a valid alternative to SAVR in these patients. One of the main characteristics of TAVI, when compared to SAVR, is that the diseased native aortic valve remains in place. For hemodynamic testing of new percutaneous valves and clinical training, one should rely on animal models. However, the development of an appropriate animal model of severe aortic stenosis is not straightforward. This work aims at developing and testing an elastic model of the ascending aorta including a severe aortic stenosis. The physical model was built based on a previous silicone model and tested experimentally in this study. Experimental results showed that the error between the computer-aided design (CAD) file and the physical elastic model was <5%, the compliance of the ascending aorta was 1.15 ml/mm Hg, the effective orifice area (EOA) of the stenotic valve was 0.86 cm2, the peak jet velocity was 4.9 m/s and mean transvalvular pressure gradient was 50 mm Hg, consistent with as severe. An EDWARDS-SAPIEN 26 mm valve was then implanted in the model leading to a significant increase in EOA (2.22 cm2) and a significant decrease in both peak jet velocity (1.29 m/s) and mean transvalvular pressure gradient (3.1 mm Hg). This model can be useful for preliminary in vitro testing of percutaneous valves before more extensive animal and in vivo tests.


Subject(s)
Aortic Valve Stenosis/surgery , Computer-Aided Design , Transcatheter Aortic Valve Replacement/methods , Aorta/surgery , Aortic Valve/surgery , Computer Simulation , Elasticity , Heart Ventricles , Pressure , Transcatheter Aortic Valve Replacement/instrumentation
5.
Med Biol Eng Comput ; 52(1): 1-8, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24037347

ABSTRACT

Calcific aortic valve disease is the most common heart valve disease. It is associated with a significant increase in cardiovascular morbidity and mortality and independently increases the cardiovascular risk. It is then important to develop parameters that can estimate the stiffness of the valve. Such parameters may contribute to early detection of the disease or track its progression and optimize the timing for therapy. In this study, we introduce a metric representing the stiffness of the native aortic calcified valve over a wide range of stenosis severities. Our approach is based on three-dimensional structural finite-element simulations and in vitro measurements. The proposed method is developed first in a pulse duplicator; its clinical applicability is then evaluated in three patients with severe aortic stenosis. Our results indicate that the value of the proposed metric varies considerably between healthy valves and valves with very severe aortic stenosis, from 0.001 to 7.38 MPa, respectively. The method introduced in this study could give useful information regarding the stiffness of the valve leaflets with potential application to the evaluation of aortic sclerosis and aortic stenosis.


Subject(s)
Aortic Valve Stenosis/diagnosis , Aortic Valve Stenosis/pathology , Aortic Valve/pathology , Calcinosis/diagnosis , Calcinosis/pathology , Computer Simulation , Early Diagnosis , Humans
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