Synopsis
This
presentation will review the data acquisition, post processing, and blood
flow quantification using standard 2D PC and 4D Flow MRI. Sources of error for
the blood flow measurements will also be analyzed.Highlights
·
Standard 2D phase contrast magnetic resonance imaging
(PC – MRI) is tipically used to quantify blood flow in the heart, through heart
valves and in great vessels.
·
4D flow MRI has the potential to provide a
comprehensive retrospective evaluation of vascular hemodynamics with full
volumetric coverage, becoming a promising tool for cardiac and vascular
diagnosis.
·
PC MRI requires prior knowledge (approximation)
of the maximum velocities that are expected in the vessel of interest to avoid
aliasing.
Target Audience
Those with interest in non-invasive
quantification of blood flow using phase contrast 2D and 4D MRI.
Objectives
· To review standard 2D PC MRI methods for
quantification of blood flow in clinical applications.
· To review advances in 4D flow MRI for flow
quantification in different vascular territories.
· To review potential limitations and potential
sources of errors for velocity mapping and parameters derived from those
measurements.
Purpose
The purpose of this
presentation will be to review the data acquisition, post processing, and blood
flow quantification using standard 2D PC and 4D Flow MRI. Sources of error for
the blood flow measurements will also be analyzed.
Methods
Cardiovascular
MRI has undergone substantial developments over the last decades and offers
capabilities for evaluating cardiac anatomy and function including cardiac viability,
perfusion, blood flow, and vascular anatomy. 2D phase contrast MRI is widely
used clinically for the noninvasive assessment of flow volumes and peak
velocities in a single plane with one-directional velocity encoding [1]. Improvements in MR hardware, sequence
design, and image reconstruction have facilitated accelerated cardiovascular imaging,
permitting to capture volumetric velocity fields with three-directional
velocity encoding over a 3D volume throughout the cardiac cycle in clinically
feasible scan times [2]. Data sets obtained from such examinations
can provide information on the anatomy, vascular lumen, and hemodynamic
information from a single acquisition. This is all inherently co-registered and
obtained in 5-20 minute acquisitions, depending on cardiac and respiratory
gating needs, spatial and temporal resolution, and volume coverage [3].
PC
MRI requires the user to define an upper velocity limit given by the velocity
sensitivity encoding parameter (Venc). Venc is defined as the (positive or
negative) maximum velocity that can be detected without error. For velocities
exceeding the Venc, velocity aliasing occurs. In this case, the acquisition needs
to be repeated with an increased Venc or antialiasing correction needs to be
performed to achieve data that can be properly quantified. PC MRI thus requires
prior knowledge (approximation) of the maximum velocities that are expected in
the vessel of interest [4].
Several
sources of error, such as background phase contributions from eddy-currents, or
method-specific problems, such as velocity aliasing and noise, can compromise MR
velocity maps and need to be addressed prior to data quantification or
visualization. Software for blood flow quantification from 2D PC MRI is widely
available and can be used for images acquired in all different platforms. In
contrast, extensive work is being done to standardize a way to quantify flow
from 4D flow MRI datasets.
Results
Blood
flow can be quantified by standard 2D CINE PC techniques that can easily be applied
during a single breath hold, which may be sufficient for several clinical
applications. On the other hand, 4D flow MRI offers the ability of
retrospective quantitative evaluation of blood flow at any location of interest
within the 3D volume (Fig1). Despite relative long scan times, on the order of 5–20
minutes (depending on heart rate, breathing compensation efficiency, and
applied sequence), 4D flow MRI inherently provides an easy scan prescription
(positioning of a single 3D volume). This may be especially advantageous in
cases where multiple breath-held 2D CINE PC MRI scans are needed such as in
congenital heart disease. Particularly in young pediatric patients, where breath-held
scans are often not feasible, the free breathing 4D flow MRI acquisition with
volumetric coverage may provide an advantage over standard MR techniques [5, 6].
Discussion and Conclusions
The methods discussed here provide
blood flow information for a wide range of cardiovascular pathologies. 4D flow
MRI has the potential to significantly change the way flow imaging is
clinically conducted, as well as expand the indications for velocity sensitive
imaging by providing unique insights into the velocity fields and additional
functional parameters. These non-invasive measures can possibly enhance
diagnosis, therapy planning, and therapy monitoring in a wide range of
cardiovascular imaging, including all major vascular territories and the heart.
Acknowledgements
We acknowledge support from the NIH (R01 DK088925) the AHA (14SDG19690010), UW Radiology R&D and GE HealthcareReferences
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