Synopsis
Diffusion
encoding along multiple directions in a single shot facilitates
probing of tissue microstructure that is not accessible with
conventional (linear) tensor encoding. However, it tends to engage
gradients on multiple axes in a pattern that yields higher energy
consumption, which can become a critical limiting factor for gradient
system performance. Here, we show that Slice Interleaved
Free-waveform Imaging (SIFI) of b-tensor size, orientation, and shape
reduces peak power consumption and heating, which translates to
markedly reduced repetition time, shorter examination times and
higher temporal SNR.
Introduction
B-tensor
encoding was recently proposed1-2
as a novel framework for diffusion weighted imaging. It enables a
novel dimension by expanding the shape of the
diffusion encoding tensor beyond conventional linear tensor encoding
(LTE) e.g. by including spherical-tensor-encoding (STE)3.
The generated data allows sources of heterogeneity to be disentangled
– yielding exciting results1.
Technically, the encoding uses free-waveform gradients, yielding
specific q-space trajectories.
Optimized waveforms5,7
are required for feasible echo times; waveforms with
the highest efficiency leverage the
full capacity of the hardware (maximal gradient strength/slew). This
operating mode puts strain on the gradients
and can result in inflated scan times due to excessive power
consumption and ohmic heating.
While
a b-tensor encoding protocol with feasible scan times was
demonstrated recently6,
any decrease in the acquisition time would benefit wider usage. So far, acquisition of different tensor
shapes was
performed in separate scans, but this complicates its use and
increases the risk for inconsistent data – specifically in
applications prone to motion and scan interruption.
This novel sequence version allows
Slice-Interleaved-Free-waveform
Imaging (SIFI) providing complete freedom in the choice of the
size, orientation, and shape of the encoding on a slice-by-slice
level. Beyond the immediate benefits of reduced scan time and higher
internal data consistency, the increased temporal sampling of low-b
slices
might improve outlier rejection, motion and distortion correction8
–
all
facilitating b-tensor encoding
in motion-rich applications.Methods
Currently,
the high demand from sustained gradient-intense volumes – requiring
the same encoding for every slice – leads to power and heating
peaks. Although they make up only a small fraction of the required
volumes, they set the required gradient cooling time and thus extend
the repetition time for the entire scan.
SIFI
breaks with two of the mentioned conventions to address this
challenge: The original free-waveform sequence1,5
(scan-interleaved) was modified (I) to allow dynamic switching
between waveforms within one scan (volume-interleaved), and (II)
to break with the traditional “one-volume one-encoding”
paradigm8.
These changes were implemented into the EPI sequence on a clinical 3T
Philips Achieva scanner to allow complete freedom in the choice of
size, orientation and shape of the encoding tensor for every slice
(slice-interleaved). Fig.1 illustrates both the volume-interleaved
version as well as slice-interleaved version on a 12-slice stack.
To
ensure usable
datasets even in interrupted acquisitions, we introduce the concept
of super-blocks – each made up
from N volumes, containing slices from N encodings9.
The whole acquisition is composed of multiple super-blocks. To
maximally spread the demands on the gradient system, each super-block
consists of interleaved high/low-demand waveforms (typically STE/LTE,
Fig.1).
The interleaving reduces peak
demand to a level within the available supply of power and cooling.
The
obtained data can be sorted to the traditional volume order.
Alternatively, the quick temporal encoding variations can be used to
facilitate motion correction for highly attenuated SNR poor higher-b
slices8.
The
parameters of the slice-interleaved version were: two b=0, and b=[100,500,1000,1800]s/mm2
in three/six directions for STE/LTE respectively; FOV=240x240mm2,
28 slices, resolution=2mm3,
TE=100ms, SENSE2, partial-Fourier=0.8,
Gmax/slew=78mT/s,
100mT/m/s,
pre180post180=38.9ms/29.4ms. The optimized5
STE waveform was
Maxwell-compensated7,
the LTE waveform chosen to maximize encoding efficiency (Fig.2).Results and Discussion
SIFI
data was acquired on a
healthy volunteer on a clinical Philips 3T-Achieva at high Gmax
without requiring
TR-extension and without producing any peripheral-nerve-stimulation
(PNS). The pilot testing was conservative as thermal load and PNS
modelling are
not yet completely automated. The initial thermal load simulations
depicted in Fig. 3 for volume-sorted, volume-interleaved and
slice-interleaved versions represent only the thermal demands based
on a basic vendor load
model8.
However, it shows the large achievable
reduction in system demand.
For the chosen example and assuming the LTE waveform on all three
axis for STE-encoding to
allow standard vendor sequence validation, the time with
volume-interleaving was reduced by factor 1.9. This is a
conservative estimate since our load modelling
indicates that STE presents higher demands than LTE. The
resulting SIFI data
is depicted before and after sorting in Fig.4, illustrating that
conventional volumes could be obtained.Conclusion and Outlook
Slice-level
interleaving of diffusion encodings is especially beneficial for
gradient waveforms operating at the hardware limit – such as in
b-tensor encoding.5
Interleaved encoding can reduce the scan time significantly. The
reduction depends largely on the chosen parameters, in the given
example with moderate b-value and only 28 slices the conservatively
estimated achieved reduction was
1.9. This
can be translated to higher angular resolution, or denser shell
sampling. Further work will involve the optimized automatic ordering
of the encodings while respecting all constrains (power, cooling and
PNS). The implementation
further allows slice-level10
adaption of the
phase-encoding-direction – expected to improve distortion
correction – as well as slice excitation order – allowing
simultaneous T1-diffusion mapping11.Acknowledgements
This
work received funding from the European Research Council under the
European Union’s Seventh Framework Programme (FP7/20072013)/ERC
grant agreement no. 319456 (dHCP project), the NIH Human Placenta
Project grant 1U01HD087202-01, the
Wellcome Trust (Sir Henry Wellcome Fellowship, 201374/Z/16/Z) and
was supported by the Wellcome EPSRC Centre for Medical Engineering at
Kings College London (WT 203148/Z/16/Z), MRC strategic grant
MR/K006355/1 and by the National Institute for Health Research (NIHR)
Biomedical Research Centre based at Guy’s and St Thomas’ NHS
Foundation Trust and King’s College London. The views expressed are
those of the authors and not necessarily those of the NHS, the NIHR
or the Department of Health.References
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