Coronary atherosclerosis is common at vessel bifurcations. A quantitative approach to measuring blood velocity, vorticity and more complex flow features at bifurcations would enhance the understanding of the mechanisms of atheroma development, and potentially predict vessels at highest risk. The aim of this work was to validate 4D phase contrast (PC) magnetic resonance imaging flow measurements using a simplified arterial model of the left main coronary bifurcation against computational fluid dynamic (CFD) modelling.
Methods
A simplified left main to left anterior descending/circumflex bifurcation phantom was created from CT angiography data using 3D rapid prototyping. This was scaled up six-fold using the laws of dimensional scaling to an inlet diameter of 25 mm and connected to a pump to create a steady flow circuit in the MR scanner. Flow was measured using 4D PC MRI on a 3T Siemens Skyra (Erlangen, Germany). Custom software (MATLAB) was developed to convert the PC grey scale images to a structured data set with spacial, 3D velocity vector and time properties. The same geometry and conditions were then digitally modelled using CFD (ANSYS CFX 13.0 and Dell T5500, 64-bit 2.13 GHz six-core Intel Xeon with 12GB RAM) and the results exported to the same structured data set for comparison. The data was registered using a least squares 3D affine transformation and tri-linearly interpolated to create a co-registered 4D volume with more than 90 million data points which was then visualised as shown in Figure 1.
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Results
The standard deviation of the differences between the PC and CFD data was less than 10%. Regional flow features such as vortices were identified in the PC data, and were found to be subjectively similar to the corresponding features in the CFD data. Regions of PC artefact were identified using the CFD results, and were associated with lower spatial resolution and background eddy current effects.
Conclusions
PC MR flow measurements show good quantitative and structural flow similarity to CFD. CFD may be useful for the identification of regions of artefact in PC data and potentially provide a means of correction or regularisation.
Funding
Auckland Heart Group Charitable Trust.
Open Access
This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License (
https://creativecommons.org/licenses/by/2.0
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (
https://creativecommons.org/publicdomain/zero/1.0/
) applies to the data made available in this article, unless otherwise stated.
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