Bulletin of the American Physical Society
71st Annual Meeting of the APS Division of Fluid Dynamics
Volume 63, Number 13
Sunday–Tuesday, November 18–20, 2018; Atlanta, Georgia
Session Q17: Biological fluid dynamics: Cardiac Flows
12:50 PM–3:00 PM,
Tuesday, November 20, 2018
Georgia World Congress Center
Room: B304
Chair: Oscar Flores, University Carlos III de Madrid
Abstract ID: BAPS.2018.DFD.Q17.1
Abstract: Q17.00001 : In vitro assessment of bioprosthetic valve performance in healthy and diseased right ventricular outflow tracts using magnetic resonance velocimetry*
12:50 PM–1:03 PM
Presenter:
Nicole Schiavone
(Stanford University)
Authors:
Nicole Schiavone
(Stanford University)
Christopher Elkins
(Stanford University)
Doff McElhinney
(Stanford University)
John K. Eaton
(Stanford University)
Alison L. Marsden
(Stanford University)
The congenital heart defect Tetralogy of Fallot (ToF) affects 1 in every 2500 newborns annually and requires surgical repair of the right ventricular outflow tract (RVOT) and subsequent placement of an artificial pulmonary valve. The longevity of these valves is highly variable and complications from ToF lead to large disparities in RVOT anatomy among patients. This work aims to assess the performance of bioprosthetic pulmonary valves in healthy and diseased RVOT geometries using magnetic resonance velocimetry. Two 3D-printed geometries were analyzed: an idealized case based on healthy subjects aged 11 to 13 and a diseased case with a 150% dilation in vessel diameter downstream of the valve. Each geometry was studied with two valve orientations: one with a valve leaflet opening posterior, which is the native pulmonary valve position, and one with a valve leaflet opening anterior. Flow features, including vortex formation and stagnation regions, are shown to be drastically different between the RVOT geometries and valve orientations. For example, in the diseased geometry, changing the valve orientation alters the jet angle at systole by 20 degrees and reduces recirculating flow around the valve throughout the cardiac cycle.
*Funded by the Stanford Child Health Research Institute.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2018.DFD.Q17.1
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