Ahsan Javed1, Rajiv Ramasawmy1, Kendall O’Brien1, Christine Mancini1, Pan Su2, Waqas Majeed2, Thomas Benkert3, Himanshu Bhat2, Anthony F. Suffredini4, Ashkan Malayeri5, and Adrienne E Campbell-Washburn1
1Cardiovascular Branch, Division of Intramural Research, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, United States, 2Siemens Medical Solutions USA Inc., Malvern, PA, United States, 3Siemens Healthcare GmbH, Erlangen, Germany, 4Critical Care Medicine Department, Clinical Center, National Institutes of Health, Bethesda, MD, United States, 5Department of Radiology and Imaging Sciences, Clinical Center, Department of Health and Human Services, National Institutes of Health, Bethesda, MD, United States
Synopsis
High-performance 0.55T MRI is
promising for lung imaging due to the reduced susceptibility artifacts.
However, high-resolution lung imaging is still challenged by low proton density
and SNR. 3D spiral acquisitions can
be used to improve SNR-efficiency, but these readouts are susceptible to trajectory
errors and blurring from concomitant-fields, which are amplified at lower field
strengths. Here we present a self-gated, ultra-short echo-time,
stack-of-spirals acquisition which leverages rapid inline corrections for
trajectory imperfections, trajectory dependent navigator signal fluctuations,
and concomitant-fields to enable robust 1.75mm isotropic lung imaging at 0.55T.
We also demonstrate our technique in healthy-volunteers, patients with lung-nodules
and COVID-19.
Introduction
High-performance low field systems are well suited for structural lung
imaging due to reduced susceptibility and prolonged T2* times1. Ultra-short echo
time (UTE) sequences are important for high-resolution structural imaging of
lungs at clinical field strengths2,3 but require
dedicated optimization for low-field systems. SNR is reduced at lower-fields
because it is proportional to field-strength. This can be mitigated by
leveraging increased T2* times to efficiently sample k-space using longer
spiral-readouts to improve SNR-efficiency. However, spiral-readouts are
susceptible to off-resonance and concomitant-field related blurring.
Off-resonance blurring scales with B0 and is therefore reduced at lower field
strengths; however, concomitant field artifacts scale inversely with B0 and are
amplified at lower field strengths4.
Our aim is to develop a robust method for free-breathing,
high-resolution pulmonary imaging at 0.55T. In this work, we optimized a self-gated
stack-of-spirals UTE sequence and leverage trajectory correction, robust
respiratory binning, and concomitant field correction to mitigate artifacts,
with corrections implemented in line for rapid image reconstruction5.Methods
Data Acquisition: A prototype free-breathing 3D T1-weighted UTE
spoiled gradient echo stack-of-spirals sequence was used for imaging on a 0.55T
MRI system (prototype MAGNETOM Aera, Siemens Healthcare, Erlangen, Germany).
Additional readouts were acquired along the superior-inferior (SI) direction to
estimate the respiratory-signal with temporal resolution of 200-300ms. All
scans used golden angle increments of spiral interleaves. Imaging parameters: TE/TR = 0.5/7.7 ms, Flip-angle (FA)
= 5, readout-duration = 5.4ms, field-of-view (FOV) = 450 x 450 x 224 mm3,
matrix-size = 256 x 256 x 112 (slice oversampling-factor = 14.2%), total
acquisition-time = 15 min 30 sec. We
also retrospectively clipped the data from the end of the scan to simulate
reduced scan times (5 min, 8.5 min, and 12 min) and its effect on image
quality. We calculated relative maximum derivative to measure image sharpness
around the diaphragm3.
Reconstruction: Respiratory waveforms were extracted from the
SI readouts using previously published methods6,7. An additional
correction for trajectory dependent fluctuations in the respiratory navigator-signal
was implemented. Data was retrospectively binned before reconstruction to
reduce respiratory motion artifacts. The threshold for binning was empirically
chosen to be 40% of the total data at the most stable respiratory phase.
Images were reconstructed inline using
Gadgetron5
on a system equipped with Dual Intel Xeon processors, 512 GB RAM, 3x Nvidia
Quadro RTX 8000 GPUs. Density compensation weights were estimated using an
iterative technique8.
We used a conjugate gradient SENSE reconstruction to reduce artifacts from
non-uniform under-sampling in k-space for binned free-breathing data.
Spiral trajectory and concomitant field
corrections: Inaccuracies in spiral trajectories
were corrected using gradient system impulse response functions9,10.
The local phase caused by concomitant fields was estimated for each spiral acquisition.
Corrections were applied using multi-frequency interpolation, whereby each
spiral acquisition was demodulated at 24-29 frequencies and a pixel-wise linear
combination of the images was used to estimate the corrected image11.
Patient imaging: Human subjects imaging was performed with
permission from the local Institutional Review Board. Informed consent was
obtained from all subjects. A total of 15 human subjects were scanned for this study; 6 healthy
volunteers, 3 patients with active COVID-19 infection, 4 patients who recovered
from COVID-19, and 2 patients with lung nodules. The image quality and artifacts were qualitatively evaluated by a senior
radiologist with 15 years of experience. Images were scored
using a 5-level Likert scale for image quality and for artifact level.Results
All reconstructions were performed in Gadgetron with reconstruction
times < 5 min. Figure 1A shows an example of the self-gated respiratory
signal with and without angular filtration. The resulting images (Figure 1B) demonstrate
reduced respiratory motion artifacts especially noticeable around the liver
dome and blood vessels with angular filtration. Improvements in image quality
from respiratory binning and concomitant field correction are demonstrated in
Figure 2 for a healthy volunteer and patient with a lung nodule.
Figure 3 shows images
reconstructed for scan times of 5, 8.5, 12, and 15.5 min in three subjects.
Overall, we did not observe significant deterioration in image quality (i.e.
significant loss in signal, or reduced visibility of anatomy) with simulated
reduction in scan-time down to 8.5 min which shows that, potentially, an 8.5
min scan is sufficient to achieve diagnostic quality images with our technique.
We also show the measured reduction in SNR and aSNR, and radiologist image
quality score from shorter scan times in Table 1.
Figure 4 shows
representative examples of maximum intensity projections (MIPs) and
single-slice images from each subject group reconstructed from the 8.5 min
acquisition. It includes a healthy volunteer, a patient with lung nodules, a patient
with acute COVID-19 infection, and a patient who had recovered following
COVID-19 infection.Discussion and Conclusion
We have presented an optimized implementation of free-breathing 3D
stack-of-spirals UTE pulmonary imaging sequence for a high-performance 0.55T
system with fast inline reconstruction. We demonstrate that a combination of
robust respiratory binning, trajectory corrections, and concomitant field
corrections are necessary to achieve diagnostic image quality in
high-resolution UTE imaging at 0.55T. Using our optimized method, we were able
to achieve high-quality structural lung imaging with a resolution of isotropic 1.75mm
in 8.5 min.Acknowledgements
The authors thank Margaret (Peg) Lowery, Jennifer Henry, Amelia Nargozian, and Doris Swaim for assistance with patient recruitment. The authors would like to thank Josef Pfeuffer for helpful discussions and assistance in design and implementation of the MR pulse-sequence used in this study. The authors would like to acknowledge the assistance of Siemens Healthcare in the modification of the MRI system for operation at 0.55T under an existing cooperative research agreement (CRADA) between National Heart, Lung, and Blood Institute and Siemens Healthcare. The study was supported by the Division of Intramural Research, NIH/NHLBI (Z01-HL006257).References
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