Grzegorz Bauman1,2 and Oliver Bieri1,2
1Department of Radiology, Division of Radiological Physics, University of Basel Hospital, Basel, Switzerland, 2Department of Biomedical Engineering, University of Basel, Allschwil, Switzerland
Synopsis
In
this work, we demonstrate the application of free-breathing respiratory
self-gated thoracic MRI with balanced steady-state free precession half-radial
dual-echo imaging technique (bSTAR) in human subjects. The technique combines
an efficient minimal-TR readout sampling with an interleaved randomly tilted
Archimedean spiral trajectory. The methodological improvements result in
high-quality visualization of pulmonary parenchyma and vessel structure. The
proposed k-space sampling scheme allows reconstruction of multi-volume data
sets at different respiratory phases.
Introduction
Despite the continuous improvement
in MR-scanner hardware and data processing techniques, thoracic MRI remains
challenging due to the problems associated with physical properties of the
lung. Nonetheless, imaging techniques such as ultra-short echo time (UTE)1,2, zero echo time (ZTE)3 or balanced steady-state free precession
(bSSFP)4 have shown compelling results in structural and functional lung
imaging. More recently, a 3D half-radial dual-echo bSSFP technique known as
bSTAR has been demonstrated to provide high-resolution and artifacts-free chest
images acquired during a single breath-hold5.
The requirement for a prolonged
breath-hold, however, can limit the feasibility of the technique especially in
children, uncooperative patients, or patients with severe pulmonary disease.
Hence, in this work we aimed at the development of a free-breathing bSTAR
technique by carefully adapting and exploiting novel k-space sampling
strategies merged with respiratory self-gating techniques.Methods
Free-breathing bSTAR
Similarly to previously presented
techniques5,6, we have implemented a 3D half-radial dual-echo acquisition
scheme using a bSSFP kernel with a non-selective rectangular RF excitation
pulse and a bipolar readout gradient. In contrast to prior work5, a single ADC
(rather than two ADCs) was used along the full bipolar readout to provide not
only full maximum sequence efficiency but also improved spatial resolution.
Data acquired during each readout comprises a center-out and a center-in
half-radial projection. Figure 1 shows the corresponding pulse sequence
diagram.
In
order to ensure a homogeneous coverage of the k-space over multiple breathing
cycles, we have applied short duration interleaves based on Archimedean spirals
rotated about the polar axis by the golden angle7. To further mitigate the
sampling periodicity with respect to the breathing cycle, each interleave is
tilted by a small random polar angle (Figure 2). Furthermore, eddy currents
were mitigated by alternating the direction of the consecutive interleaves
traversing the k-space along the azimuthal axis, which allows avoiding large jumps in the k-space.
MR data acquisitions
Experiments were performed at 1.5T
(MAGNETOM Avanto-Fit, Siemens Healthineers, Erlangen, Germany). Five healthy volunteers (mean age:
36.6 years, range: 27-53 years, three male, two female) were scanned with the
proposed free-breathing 3D bSTAR implementation and a single breath-hold 3D
bSTAR for comparison. The study was approved by the Institutional Review Board.
All scans were performed with
predefined shim settings, field-of-view = 35x35x35 cm3, TE1/TE2/TR =
0.11/1.18/1.39ms, 320 samples per half-radial projection, 150us hard RF pulse,
flip angle α = 20º, 1856Hz/pixel bandwidth. For free-breathing bSTAR (FB-bSTAR)
240000 half-radial projections were acquired using 240 interleaves, which
resulted in scan time of 5.6min. The breath-hold bSTAR (BH-bSTAR)
acquisition took 23 seconds with 17000 half-radial projections and 12
interleaves. The pulse sequence efficiency (fraction of TR devoted to sampling
the signal) was 0.78.
Image reconstruction
bSTAR datasets were reconstructed
off-line using compressed sensing with a fast iterative shrinkage-thresholding
algorithm (FISTA-Mod)8. The datasets were reconstructed on a 3843
matrix resulting in 1.4 mm isotropic resolution matching the spatial resolution
measured in the k-space. Reconstruction of the breath-hold bSTAR resulted in a
single 3D volume. For the reconstruction of the FB-bSTAR, k-space center
modulation of a coil located near diaphragm was used to derive the respiratory
signal modulation. Readouts acquired during multiple breathing cycles were
binned into 10 respiratory phases and reconstructed as separate 3D volumes. The
reconstruction pipeline was written in C++ with CUDA Toolkit 11 (NVIDIA Corp.
Santa Clara, CA) on a workstation equipped with Quadro P6000 GPU (NVIDIA Corp.).
Results
Figure 3 shows exemplary FB-bSTAR
reconstructions: a composite image (no gating) along with three different
respiratory phases (inspiratory phase, intermediate phase and expiratory phase),
as well as an end-expiratory BH-bSTAR acquisition for comparison. The
effectiveness of the respiratory self-gating as compared to a breath-hold
acquisition is shown in Figure 4. The signal amplitude profile extracted at the
diaphragm position from the FB-bSTAR closely matches the profile obtained in
BH-bSTAR. Maximum intensity projection images (15mm) acquired in a healthy
volunteer using BH-bSTAR and FB-bSTAR are shown in Figure 5. The pulmonary
vascular structure is well visualized using both the breath-hold and free-breathing
bSTAR acquisitions.
Discussion and Conclusion
In this work, we have
demonstrated the feasibility of free-breathing 3D bSTAR thoracic imaging with
respiratory self-gating in a small group of healthy subjects. Retrospective
self-gating represents a major technical improvement of bSTAR imaging and is
especially important for less compliant patients. Furthermore, it allows for
the reconstruction of different respiratory phases from a single dataset to
derive functional parameters related to lung parenchyma density changes or
tissue motion. Future studies will focus on the clinical application of our free-breathing
bSTAR technique in patients with pulmonary disease.Acknowledgements
No acknowledgement found.References
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