Ummul Afia Shammi1, Zhijian Luan2, Jia Xu3, Aws Hamid4, Joanne Cassani4, Talissa A. Altes4, Robert P. Thomen4, and Steven R Van Doren5
1Biomedical, Biological & Chemical Engineering, University of Missouri, Columbia, MO, United States, 2Institute for Data Science and Informatics, University of Missouri, Columbia, MO, United States, 3Biochemistry, University of Missouri, Columbia, MO, United States, 4Radiology, University of Missouri, Columbia, MO, United States, 5Biochemistry, Institute for Data Science, University of Missouri, Columbia, MO, United States
Synopsis
Two new methods of
automatic, retrospective suppression of breathing motion appear to be effective
for real-time cardiac MR (CMR) scans of free-breathing healthy volunteers. This
may obviate the need for multiple breath-holds during CMR exams, allowing for a
quicker, more comfortable experience for cardiac patients. The first method
demonstrated corrects smaller breathing motions and has the advantage of
correcting all cardiac cycles. The second method demonstrated successfully compensates
the respiratory excursions of largest amplitude, common in short axis scans, by
extracting cardiac cycles at end-inspiration or end-expiration.
Background
If cardiac
MR (CMR) could be acquired during free breathing with retrospective
correction of the breathing
motion (1, 2), the
exam would be shorter and more comfortable for patients, compared to CINE during
breath holds. In real-time
CMR, large-amplitude motions at end-inspiration present an especially high
hurdle for post-processing to surmount. We developed software to retroactively suppress
frame-to-frame heart displacement by respiration, even at end-inspiration.Methods
Real-time
CMR scans of healthy volunteers were acquired during free-breathing on a 3T Siemens
Magnetom Vida scanner using
a bSSFP sequence (3–5). Compressed Sensing (6) increased the time resolution of short- and
long-axis images to 22 frames/sec (208×170 matrix, voxel size 1.5-1.7×1.5-1.7×6
mm3). Software development began from the TREND package that tracks and resolves multiple concurrent
changes between images and spectra using unfold principal component analysis (7). We tailored TrendCMR not only to resolve
concurrent cardiac and respiratory motions in dynamic MR scans, but also to
make automatic decisions to reconstruct DICOM files with less frame-to-frame displacements
of the heart by respiratory motions. Two methods were developed for
retrospective removal of breathing motion: Method 1 reconstructs the entire
scan with automatic removal of the main breathing motions. Method 2 minimizes
the impact of breathing motion by locating and selecting cardiac cycles at end-inspiration
or end-expiration and reconstructing separate segments of the scan. Image congruence
before and after motion correction was quantified as the correlation
coefficient between a frame in systole and the equivalent frame from every
other cardiac cycle.Results
TrendCMR
resolved dozens of concurrent motions as principal components (PCs) present in
free-running CMR scans of healthy volunteers (Fig. 1A). Power spectra of time
courses of the PCs enabled automatic identification of PCs dominated by
breathing (Fig. 1B), for omission from reconstructions by Method 1. Method 1 improved
the beat-to-beat consistency, making it appealing for correction of entire
scans with smaller breathing amplitudes, typical of long axis views, as evident
from the improved correlations among beats (Figs. 2, 3C). However, at high-amplitude
breathing motions in short axis views, Method 1 introduced ghosts at end-inspiration
during systole (Figs. 2B, 4C). To manage high-amplitude excursions, cardiac
cycles were grouped by respiratory phase (Method 2). Since there was no
triggering during acquisition, each frame’s position within the cardiac cycle
was identified retrospectively in the time course of the main cardiac PC, after
correcting its sign to make the increased brightness of diastole positive (Fig.
5A). Large breathing motion shifted and decreased apparent amplitude of
the cardiac cycle in time courses of the main cardiac PC at end-inspiration (Fig.
5A). At such large and challenging inspirations, an additional automatic search
for cardiac cycles was conducted. The heartbeats coinciding with end-expiration
in the main respiratory PC (Fig. 5B) were selected for construction of the
end-expiratory portion of the scan, and likewise for heartbeats during
end-inspiration (Fig. 5B). The excerpts of the original scan obtained by Method
2 retained full cardiac image quality, with suppression of breathing motion that
is very good during end-inspiration and excellent during end-expiration (Figs.
3D, 3E, 4D, 4E). While displacement fields of free-running vertical long axis
and short axis scans are dominated by respiratory movement of the heart (Figs.
3F, 4F), after correction by Method 2 their displacement fields are dominated
by cardiac motions (Figs. 3G, 3H, 4G, 4H). In order to quantify and compare the
reproducibility and clarity of cardiac cycles after motion correction by Method
1 or 2, we computed the minimum correlation of each beat with the other beats
in that reconstruction, and in the original scan. Method 1 consistently boosted
the reproducibility of the beats across the full length of the scan (min.
correlation coefficients of 0.90 to 0.965; e.g., Figs. 3I, 4I), with exceptions
noted in Fig. 2B, 4C. Method 2 improved
the correlation coefficients of inspiratory beats to levels comparable to
Method 1 (min. correlation coefficients of 0.92 to 0.985), with sometimes
greater clarity. In the case of expiratory beats, Method 2 increased their
correlation coefficients, reproducibility, and clarity to minimum correlation
coefficients of 0.95 to 0.99 (e.g., Figs. 3I, 4I).Discussion
Here
we demonstrate that respiratory motions in free-running CMR can be suppressed
by either Method 1 that reconstructs a simplified scan or method 2 that
retrospectively navigates to cardiac cycles during end-inspiration and
end-expiration. The combination of expedited free-breathing CMR with either method
offers the potential to facilitate CMR scanning of patients non-compliant to breath-holding
in CINE protocols. This includes patients too frail for multiple breath holds
and patients with arrhythmias unsuitable for averaging. Free-running
acquisitions combined with retrospective motion correction create the
possibility of assessing how cardiac cycles may vary with respiratory phase. To
compensate for the limitations of Method 1 during high-amplitude excursions,
subjects could be asked to breathe in a shallow manner during short-axis scans. Conclusions
Two
methods of retrospective removal of breathing motion in real-time cardiac MRI
have been developed and demonstrated. Method 1 removed breathing motion from
the entire scan, but during large inspirations introduced ghosts. Method 2 consistently provided sharp images
relatively free of respiratory fluctuation, but only during end-inspiration and end-expiration. Users may prefer
Method 2 for free-breathing CMR. Acknowledgements
This study was supported by the MU Coulter Biomedical Accelerator Program, and additionally by American Heart Association grant 19IPLOI34760520.References
1. Kellman P, Chefd’hotel C, Lorenz CH, Mancini C, Arai AE,
McVeigh ER: Fully automatic, retrospective enhancement of real-time acquired
cardiac cine MR images using image-based navigators and respiratory motion-corrected
averaging. Magn Reson Med 2008; 59:771–778.
2. Usman M, Atkinson D, Odille F, et al.: Motion corrected
compressed sensing for free-breathing dynamic cardiac MRI. Magn Reson Med
2013; 70:504–516.
3. Bieri O, Scheffler K: Fundamentals of balanced steady
state free precession MRI. J Magn Reson Imaging 2013; 38:2–11.
4. Chavhan GB, Babyn PS, Jankharia BG, Cheng H-LM, Shroff MM:
Steady-State MR Imaging Sequences: Physics, Classification, and Clinical
Applications. RadioGraphics 2008; 28:1147–1160.
5. Schär M, Kozerke S, Fischer SE, Boesiger P: Cardiac SSFP
imaging at 3 Tesla. Magn Reson Med 2004; 51:799–806.
6. Lustig M, Donoho D, Pauly JM: Sparse MRI: The application
of compressed sensing for rapid MR imaging. Magn Reson Med 2007;
58:1182–1195.
7. Xu J, Van Doren SR: Tracking Equilibrium and
Nonequilibrium Shifts in Data with TREND. Biophys J 2017;
112:224–233.