S. Kozerke et al., Visualization of flow patterns distal to aortic valve prostheses in humansusing a fast approach for cine 3D velocity mapping, J MAGN R I, 13(5), 2001, pp. 690-698
The fluid dynamic performance of mechanical heart valves differs from norma
l valves and thus is considered related to late clinical complications in p
atients. Since flow patterns evolving around heart valves are complex In sp
ace and time, flow visualization based on time-resolved 3D velocity data mi
ght add important information regarding the performance of specific valve d
esigns In vivo. However, previous cine 3D techniques for three-directional
phase-contrast velocity mapping suffer from long scan duration and therefor
e might hamper assessment In patients. A hybrid 3D phase-contrast sequence
combining segmented k-space acquisition with short EPI readout trains is pr
esented with its validation in vitro. The technique was applied to study fl
ow patterns downstream from a bileaflet aortic prosthesis in six patients.
Navigator echoes were incorporated for respiratory motion compensation. Bef
ore flow visualization, spurious phase errors due to concomitant gradient f
ields and eddy currents were corrected. Flow visualization was based on par
ticle paths and animated velocity vector plots. Dedicated algorithms for pa
rticle path Integration were implemented to account for the considerable mo
tion of the ascending aorta during the cardiac cycle. A distinct flow patte
rn reflecting the valve design was observed closest to the valve during ear
ly flow acceleration. Reverse flow occurred adjacent to high velocity jets
and above the hinge housings. Later in systole, flow became confined to the
central vessel area and reverse flow along the inner aortic curvature deve
loped. Further downstream from the valve, flow patterns varied considerably
among patients, Indicating the impact of varying aortic anatomy In vivo. I
t Is concluded that MR velocity mapping is a potential tool for studying 3D
flow patterns evolving around heart valve prostheses in humans. (C) 2001 W
iley-Liss, Inc.