Maria Aristova1, Jianing Pang2, Liliana Ma1, Michael Markl1, and Susanne Schnell1
1Radiology, Northwestern University, Chicago, IL, United States, 2Siemens Healthcare, Chicago, IL, United States
Synopsis
Dual-venc
4D flow MRI has previously been reported to achieve wide velocity dynamic
range while maintaining a high velocity-to-noise ratio, which is particularly relevant for neurovascular applications. To increase flexibility in spatiotemporal resolution, we present a prototype implementation of a interleaved 8-point dual-venc 4D
Flow acquisition with independently prescribed (prospectively undersampled) spatial
resolution of the high venc acquisition, i.e. Variable Spatial Resolution Dual
Venc (VSRDV). This allowed anti-aliasing
error rates less than 15% error for a high venc spatial resolution of 70-80%.
This represents 10-15% reduction of scan time.
Introduction
Dual-venc
4D flow MRI [1] has previously been reported to achieve wide velocity dynamic
range while maintaining a high velocity-to-noise ratio. However, spatiotemporal
resolution may be compromised in order to acquire dual venc data within
clinically feasible scan times. Given that the high-venc data are only used for
velocity aliasing correction, we hypothesize that the spatial resolution of the
high-venc acquisition could be reduced in order to shorten the scan time, while
still providing adequate information to correct velocity aliasing in the high-resolution,
low-venc data. This approach has been investigated using retrospective
undersampling of sequentially acquired low- and high-venc radial PC-VIPR [2],
and a 2D phase-contrast implementation with interleaved 8-point dual-venc
encoding [3]. Here we present a prototype implementation of a interleaved 8-point
dual-venc 4D Flow acquisition with independently prescribed (prospectively
undersampled) spatial resolution of the high venc acquisition, i.e. Variable Spatial
Resolution Dual Venc (VSRDV).Methods
VSRDV
4D Flow was implemented in an 8-point dual-venc 4D Flow sequence with Cartesian
sampling and variable phase-encoding resolution of the high venc acquisition
(Figure 1). Reconstruction of both high- and low-venc images, Maxwell term
correction, and low-venc velocity aliasing correction were integrated into the
online reconstruction pipeline. The sequence was tested at 1.5 T (MAGNETOM Aera,
Siemens Healthcare, Erlangen, Germany) on two in-vitro setups: a simple tube phantom
with constant flow (Figure 2) and a realistic neurovascular anatomical replica phantom
with pulsatile flow (Figure 3). Phase-encoding resolution of the high-venc acquisition
was varied from 100% (used as reference) to 50% of that of low-venc with all other
parameters identical. Performance was evaluated by the correct identification
of aliased voxels. A comparison of flow and velocity measurements across
multiple planes in each imaging volume was also performed. Results
In
the tube phantom antialiasing error rate and specificity were within 15% of reference
for high venc resolution values of 70, 80, and 90%. However, sensitivity was
below 85% for all VSRDV values tested. Bland-Altman analysis for flow showed
bias within 15% for VSRDV resolution of 60% and above; however, peak velocity
showed high bias for all VSRDV resolutions tested. In the anatomical phantom antialiasing
error rate and specificity were within 15% of reference for all high venc
resolution values tested; sensitivity was lowest for 80% sampled data.
Bland-Altman analysis for flow and peak velocity showed bias substantially
within 15% for all VSRDV values in all vessels examined, except flow bias in
the BA at 50% VSRDV.Discussion
Flow
and velocity measurements for the tube phantom were within 15% of the reference
for high-venc spatial resolutions of 70-80% and above. Flow and velocity
measurements for the anatomical phantom were within 15% of the reference for high-venc
resolutions of 80% and above. One potential confounding factor was segmentation error, though segmentations were based on the 100% sampled dual-venc data set. Conclusion
We
successfully implemented a variable spatial resolution dual venc sequence, which
allowed anti-aliasing error rates less than 15% for a high venc spatial
resolution of 70-80%. This represents 10-15% reduction of scan time. VSRDV
provides an opportunity for decreasing scan time required for dual-venc 4D Flow
MRI while allowing to maximize temporal resolution and maintaining data
quality. This may contribute to increased clinical applicability. Future work
includes integration with acceleration methods such as GRAPPA, optimization of
dual-venc phase unwrapping schemes and post-processing methods for VSRDV, and investigation
of in-vivo performance.Acknowledgements
NIH
F30 HL140910 (Aristova)
NIH T32 GM815229 (Northwestern)
NHLBI F30HL137279 (Ma)
NIH R01 HL117888 (Markl)
NIH R21NS106696 (Schnell)
AHA
16SDG30420005 (Schnell)
Circle
of Willis model loan from United Biologics; Northwestern Research Shop staff.References
1.
Schnell et al. J Magn Reason Imaging 2017;46:102–114. DOI: 10.1002/jmri.25595
2. Nett et al. J
Magn Reson Imaging. 2012 Jun; 35(6): 1462–1471. DOI: 10.1002/jmri.23588
3.
Aristova et al, Dual-venc phase contrast MRI with increased flow encoding
efficiency. In: proceedings of the 28th ISMRM. Montréal, QC, Canada.
May 11-16 2019.