Clarissa Zimmerman Cooley1,2, Patrick C McDaniel1,3, Jason P Stockmann1,2, Sai Abitha Srinivas1, and Lawrence L Wald1,2,4
1Athinoula A Martinos Center for Biomedical Imaging, Dept. of Radiology, Massachusetts General Hospital, Charlestown, MA, United States, 2Harvard Medical School, Boston, MA, United States, 3Dept. of Electrical Engineering, Massachusetts Institute of Technology, Cambridge, MA, United States, 4Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA, United States
Synopsis
Access to MRI scanners is limited by cost, size, and siting
requirements. Specialized low-cost, compact, portable systems could greatly
increase accessibility worldwide and enable point-of-care MRI. We present a
portable MRI scanner for human brain imaging based on a compact 122kg Halbach
cylinder with a built-in readout field. Designing for a built-in encoding field
reduces the size of the magnet, the overall system power-consumption, cooling
requirements, and acoustic noise. The generalized reconstruction method
accounts for non-linearities in the gradient fields. T1 and T2-weighted in vivo
images are presented with a resolution of 2x2x7mm.
Introduction
Access to MRI is limited by cost, size, and siting
requirements. Specialized portable systems could increase accessibility and
enable point-of-care (POC) MRI. We developed a head-only, portable, low-field
MRI scanner based on a compact permanent magnet array (Figure 1a) weighing 122kg.
The scanner operates from a standard wall outlet, requires no cooling, and all
components are mounted on a cart that could be transported to a patient’s room.
Building off of previously described design stages1–9, here we present the overall
approach and in vivo brain imaging validation. Methods
The
prototype scanner shown in Figure 1 uses a sparse array of NdFeB magnets in a
Halbach cylinder configuration. Instead of maximizing homogeneity, the design
was optimized to tailor the field variation into a favorable gradient field for
read-out encoding7. This
was initially done with a genetic algorithm for the 1” cube NdFeB arrangement7, followed by a shimming stage with smaller
NdFeB elements9. Figure 2a shows the magnetic field-maps,
including the built-in (non-linear) readout field. The average B0
field is 80mT and the Y gradient is ~7.6mT/m. The built-in gradient limits the sequences to spin-echoes (RARE), but
allows standard T2, IR-prepped T2, T1, proton
density (PD) and diffusion contrasts. The built-in gradient design reduces the magnet
cost and weight and the system’s acoustic noise and power/cooling needs
(associated with a readout gradient coil in an inhomogeneous field).
Generalized projection imaging was previously presented by
rotating the magnet4,5. However, here we present imaging using
efficient gradient coils for phase encoding in X and Z. Unlike the readout, phase encoding gradients
in a spin-echo sequence need not dominate the B0 inhomogeneity since
this is refocused in the spin-echo. The compact gradient coils were designed on
the surface of a cylinder that fits tightly in the magnet bore (Fig. 3a). A BEM stream function method was used to optimize
the surface current density for linearity in the ROI8. The efficiencies of the gradient coils are
Gxeff = 0.6mT/m/A and Gzeff = 0.8mT/m/A. Less than 10A is used to drive the
coils at a low-duty cycle (3-5%), allowing for passive air-cooling.
To correct for imperfections in the compact magnet and
gradient coil field patterns, we apply a model-based generalized image
reconstruction technique that corrects distortion, a popular method used with
non-linear encoding fields10–12,4. The encoding model uses the
measured field-maps of the built-in readout gradient (Fig. 2a) and the gradient
coils (Fig. 2b,c), and models the encoding process in our 3D RARE sequences.
The sequences use a RARE spin-echo train with
frequency-swept WURST RF pulses13. For T2-weighting, the X-dimension (partition)
phase encoding is performed along the echo train with a linear k-space
trajectory. The Z-dimension gradient phase encoding is incremented linearly shot
to shot. In vivo T2-weighted results
shown in Figure 4 use a TR/TEeff of 3s/167ms, 23 PEs in X, and 97 PEs in Z,
yielding image resolution ~2x2x7mm. The
proton density sequence uses a “center-out” k-space ordering down the
echo-train, yielding a TEeff = 14ms. T1 sequence is similar but includes an IR
prep; TR/TEeff/TI = 1.8s/14ms/400ms for in vivo results in Fig. 4. Peak currents of 9A and 4.5A were used to the
drive the Z and X gradient respectively.
A spiral helmet coil5 was used for Tx/RX with an
asymmetric 12 turn distribution to improve B1 homogeneity and BW = 70 KHz
(Fig. 3b). A 50hm, 37db gain
pre-amp (MITEQ model AU-1583) and second stage 24db gain amplifier
(Minicircuits ZFL-500LN+) were used for the receiver. Additional hardware includes: a Tecmag Bluestone console, AE Techron 7224
gradient amplifiers, a 2kW-rated RFPA (Tomco BT02000-AlphaS-3MHz), and patient
table constructed from aluminum strut.
Results
Preliminary
images from healthy subjects acquired in a shielded environment are shown in
Figure 4. The images have 2mm in-plane
resolution and 7mm thick partitions. The
T2 images were acquired in 19:24 minutes with 4 averages to improve SNR. The
T1-weighted images were acquired in 11:46 minute with 2 averages. Figure 5 shows a reconstructed image assuming
all linear encoding fields and the same data using the generalized model reconstruction.Discussion
Although
some distortion is visible in all the images, Fig. 5 demonstrates the
importance of the model-based reconstruction using measured encoding fields. These
first images were acquired in a shielded room. Work is ongoing in suppressing
RF interference through the combination of passive shielding around the magnet
and active suppression in post-processing using external coils or electrodes. Work is also ongoing to replace high-cost
equipment (console, RF amplifier and gradient amplifiers), with specialized
low-cost options14–16. Conclusion
We present
our portable MRI scanner for POC operation with in vivo brain imaging validation.
Such a system could extend the reach of MRI into unconventional locations, such
as ERs, ICUs, neonatal ICUs, and rural clinics. Our in vivo results demonstrate
an image quality that is sufficient for monitoring and diagnosing many pathologies.
Future work includes imaging studies with neurology patients at MGH.Acknowledgements
We would like to thank Monika Śliwiak for her
contributions and Matt Rosen and Neha Koonjoo for assistance with the spiral
head coil. Funding from NIH NIBIB R01EB018976 and
5T32EB1680.
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