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Diffusion-Weighted Imaging at 0.064 T
Rafael O'Halloran1, Hadrien Dyvorne1, Laura Sacolick1, Jo Schlemper1, Michal Sofka1, Sadegh Salehi1, Samantha By1, Riana Schleicher2, Edmond Knopp1, Kevin Sheth3, and W. Taylor Kimberly2
1Hyperfine, Inc, Guilford, CT, United States, 2Neurology, Massachusetts General Hospital, Boston, MA, United States, 3Yale New Haven Hospital, New Haven, CT, United States

Synopsis

A sequence is described for DWI on a portable, 0.064T scanner. Images in a healthy subject and a patient with pathology are shown.

Introduction

Conventional MRI is impractical in many settings because of its cost, siting needs, weight, and power consumption. This motivates the development of low cost, portable, MRI systems [1, 2, 3]. Design constraints limit such systems to low-field, making SNR a key consideration. While lower SNR makes diffusion-weighted imaging (DWI) a challenge, DWI at field strengths as low as 0.064T has been used to successfully image stroke [4, 5]. Here we describe a DWI sequence and associated artifact mitigation strategies that are practical for use in a portable, low-field, MRI system. We show image quality obtainable in a laboratory environment in a healthy volunteer as well as a case with clinically relevant pathology obtained in a hospital setting at the point-of-care.

Methods

MRI: Data were acquired on a 0.064 T portable system (Swoop, Hyperfine Inc, Guilford, USA) with max gradient 24mT/m. The diffusion-weighted sequence was a dual spin echo 3D fast spin echo sequence (Figure 1). Parameters were: TR=1s, TE=90ms, echo spacing 4.8ms, echo train length of 40, b=90 0s/mm2, 22 x 18 x 20 cm, resolution = 2.4x 2.4 x 6mm, scan time=8.5 min, with diffusion encoding direction along the patient’s A/P axis. Encoding was Cartesian along the readout and a pseudo random sampling in the phase-slice directions, and oversampled by 5X to get sufficient SNR. Due to a large amount of steel the system has many uncompensated eddy currents, so an eddy current preparation (Figure 1a) was added to set the system in a steady state prior to the DWI prep. Diffusion encoding was performed with shaped bipolar pulses (Figure 1b). The first two echoes were used as navigators to correct for rigid body motion (Figure 1c). After the echo train (Figure 1d) a low tip angle free induction decay (FID) was collected to correct for thermal drift in the magnet blocks, followed by a degaussing block that resets the hysteresis state of the system (Figure 1e). In addition to the eddy current precompensation a hysteresis correction is performed [6]. Low b-value images (b=10s/mm2) are acquired at a scan time of 2 min and used to compute apparent diffusion coefficient (ADC) maps.
Reconstruction: Image data were denoised with sensor based denoising [7]. Next the navigator echoes are used to phase correct each echo train [8] separately for even and odd echoes using the respective navigators. The even and odd echoes are treated separately in the system due to uncorrected eddy currents that cause differential warping between the two. Even and odd echoes are separately reconstructed with an iterative SENSE reconstruction [9] and then registered using advanced normalization tools library [10]. Images were also denoised using deep convolutional neural network based denoising (DL) [11].
Human subjects: A healthy volunteer (M/39 y.o.) was scanned under IRB. A second subject (M/68 y.o.) presented comatose to the Massachusetts General Hospital (MGH) emergency department with a CT diagnosis of right thalamic hemorrhage extending into ventricles.

Results

Healthy volunteer: Figure 2 shows image quality in a healthy volunteer without DL denoising. Due to the single readout direction the white matter shows evidence of anisotropic signal as expected in the high-b-value image (Figure 2a). The low-b-value image (Figure 2b) has T2 weighting, but with lower CSF signal than expected due to short T2 (1s).
Patient with pathology: Imaging was completed at the bedside following admission from the ED. The DWI scan shows a clinically unexpected acute ischemic infarct (Figure 3, green arrows) in the right temporo-parietal region of the brain, in addition to the right thalamic intraparenchymal hemorrhage (Figure 3, blue arrows). The contrast in the lesion is notably higher than any observable white matter anisotropy effects demonstrating that the anisotropy in the white matter does not hinder visualization of the ischemic pathology. Hypointensity on ADC (Figure 3c, green arrow) confirms restricted diffusion in the ischemic lesion. DL-based denoising (Figure 3 d,e,f) improves the appearance of the images while maintaining the depiction of the lesions.

Discussion and Conclusion

There are some differences in the appearance of these images to a conventional, high field DWI. In the interest of time, a single encoding direction was used. One limitation of this approach is the detection of normal white matter anisotropy. For the application of stroke it can be a challenge to interpret, although as it was in the case shown, stroke pathology has a higher contrast than white matter anisotropy. Fat-suppression is not used due to the lack of EPI ghosting. Also due to the lack of EPI readout and low field there is no T2* contrast in the b=0 images. This must be noted to radiologists interpreting the images so that they do not assume they will be able to see bleeds on the low-b-value images.
In conclusion we demonstrated the features of a DWI sequence implemented on a portable, low-field MRI system. While the resolution and SNR are lower than a conventional system, this sequence was able to detect clinically relevant pathology. In settings where conventional imaging is unavailable, impractical, or simply not feasible in a timely manner, this sequence may provide clinicians with a valuable diagnostic tool.

Acknowledgements

No acknowledgement found.

References

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Figures

Figure 1: The sequence diagram for the DWI acquisition. (a) Eddy current preparation, (b) diffusion preparation, (c) navigators for phase correction, (d) imaging echo train and navigator for thermal drift, and (e) degaussing to set the hysteresis state. (f) Sampling is pseudorandom in the phase-slice plane in k-space and Cartesian in the readout direction. Echo ordering is radial out.

Figure 2: (a) DWI (b=900), (b) the low b-value (b=10) and (c) the ADC image in a healthy subject without DL denoising. White matter anisotropy can be noted in the high b image (a, green arrow) as well as the ADC (c, green arrow), especially in the corpus callosum. The fat signal is present due to lack of fat suppression (a, white arrow).

Figure 3: (a) The high b-value image (b=900), (b) the low b-value (b=10) and (c) the ADC map in a patient with a right thalamic hemorrhage that extends into the ventricles (a,b, blue arrows) and large vasospastic infarct (a,c, green arrows). Contrast in the infarct is quite high on the high b-value image (a, green arrow) as well as on the ADC map (c, hypointensity, green arrow). Denoising with DL (d,e,f) preserves the appearance of the pathology

Proc. Intl. Soc. Mag. Reson. Med. 30 (2022)
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DOI: https://doi.org/10.58530/2022/0043