Cyril Tous1, Martin Nicoletti2, Augustin Ogier1, Chris W Roy1, Jerome Yerly1, and Matthias Stuber1
1Universite de Lausanne, Lausanne, Switzerland, 2universite de Lausanne, Lausanne, Switzerland
Synopsis
Keywords: Pulse Sequence Design, Cardiovascular
Motivation: Designing optimal gradient waveforms is a convex problem. They must satisfy gradient hardware constraints, physiological constraints, and being time-optimal.
Goal(s): By shortening TE, we are more robust to motion artifact and less vulnerable to field inhomogeneities. By shortening TR and consequently TA, we can potentially minimize banding artifacts and obtain shorter scan time, increasing motion artifact robustness.
Approach: The gradient optimized method “GrOpt” was integrated directly into free-running 3D-radial-bSSFP and GRE acquisitions at 3T
Results: We achieved 14.0 %, 5.7% and 5.4% reduction in TE, TR and TA for bSSFP and 25.1%, 6.6% and 6.5% reduction in TE, TR and TA for GRE, .
Impact: In 3D-radial-bSSFP, CVX achieves 14.0%, 5.7% and 5.4% reduction in TE, TR and TA, respectively. In 3D-radial-GRE, 25.1%, 6.6% and 6.5% reduction in TE, TR and TA
was obtained, reducing the effect of inhomogeneities, motions, eddy current
and scan time.
INTRODUCTION
Typically,
gradient waveforms are created by combining analytical solutions and timely activation of the gradients separately on each
axis. This approach complicates the process of programming pulse sequences and
is also time-consuming. As a result, most commercial MRI pulse sequences do not
exploit the available gradient hardware or efficiently address physiological
interference. Consequently, MRI inherent hardware capabilities are not always
fully leveraged. The problem to design gradient waveforms which satisfy
gradient hardware constraints is convex (CVX), physiological constrains
(Peripheral nerve stimulation (PNS), SAR) do exist, while the requirement for being
time-optimal and sustaining desired imaging parameters (e.g. without eddy
current artefacts) needs to be satisfied. GrOpt [1–3], a gradient optimizer function, can solve this
convex problem. To this day, this technique has not been implemented either in
3D-radial-bSSFP or GRE sequences in the free-running framework
[4,5]. Such sequence provide cardiac and respiratory
motion-resolved whole-heart 5D imaging for the assessment of anatomy, function [5,6], and blood-flow [7,8]. A first insight on how CVX optimization could benefit a
free-running sequence through TE, TR, TA, PNS, and eddy current minimization is
presented for GRE and bSFFP.METHODS
Eddy currents can be simulated according to a time constant
λ as [9]:
Eddy(λ) = \integral_{Texcite}^{TE} dG/dt * e^(-t/λ) dt (1)
where the derivative of the gradient G, the slew rate, is
integrated from the RF pulse excitation to the TE. PNS constraints was
determined from the SAFE model [10]:
SAFE(G(t)) =
α1 |e^(-t/τ1)*dG/dt|+
α2 |e^(-t/τ2)*dG/dt|+
α3 |e^(-t/τ3)*dG/dt| (2)
where
αi represent the weight on each slew rate axis
and
τi are their respective time constants. According
to [2], they can be approximated to α1=0.898ms,
α2=0.097ms,
α3=0.74ms and
τ1=0.16ms,
τ1=0.74ms and
τ1=0.16ms.
The slew rate and PNS were compared, based on their maximum
allowed limit, by simulating the equations (1 and 2) into the gradient
activation timeline with and without optimization.
Two volunteers were imaged at 3T (Prisma) with free-running
bSSFP and GRE sequences with and without CVX optimization. Table 1
presents the acquisition parameters for these sequences, where TR represents the cumulative TR from all the minTR at each phase encoding steps. For non-optimized
sequences, the “normal" gradient mode (34mT/m) was selected. For optimized sequences,
the CVX gradients in the entire sequence were
designed to account for maximum gradient amplitude (80mT/m*95%), slew
rate available (80/(80*5.3)*1000*95%= 179 mT/m/ms) and raster time (10us). PNS threshold was 1. A 95% factor
was included to allow gradients to start. Finally, we aim to quantify the gain in TE,
TR and TA for each sequence and qualitatively assess image differences.RESULTS
For GRE, we were able to decrease the TE, TR, and TA by 25.1%, 6.7% and 6.5%, respectively
(TE=1.25ms, TR=77.2ms, TA=2:39min). In bSSFP,
we were able to decrease the TE, TR, and TA by 14.0%, 5.7% and 5.4%, respectively (TE=1.41ms, TR=100.5ms, TA=3:27min). During ramp time in
the GRE sequence (Figure 1), the slew rate and PNS clipped to the
maximum allowed limit using CVX. Without CVX all the gradients were derated if
one of them reached the limit. Although CVX showed a TE and TR decrease by 25.14% and 6.65%, it did not allow to improve blood to myocardium contrast on GRE images(Figure
2). Despite a 14% gain in TE and a 5.7% improvement in TR for bSSFP after CVX(Figure 3), the tradeoff between the required high RF excitation angle of
70° for SNR in bSSFP led to
incompatible SAR, which forced the TR to increase to 250ms. As a result, bSSFP showed severe
banding artefacts (images not shown). The acquisitions were slab-selective
resulting in increased eddy current response on the Gz axis(Figure 4).Discussion
After
CVX, TE was reduced by 25% in GRE and inhomogeneities were reduced.
The absence of changes in blood to myocardium contrast on GRE CVX
images is attributable to the Ernst angle (FA=4° at T1=1471ms and T2=45ms at 3T) that
maximizes SNR but not CNR. TE could be
further reduced by 0.7ms(70% shorter) using the mpVERSE pulse [2], which would lead to reduced T2*dephasing and SNR gain. Further
improvements could be made by nulling eddy current at a desired
time constant (during readout). TR and TA were also reduced to some extent (6%),which may reduce motion artefacts, and could be advantageous for long scan time
such as in 5D flow imaging.Conclusion
Convex optimization of the gradients with integrated GrOpt toolbox
directly implemented in the free-running sequence allows to fully exploit the
MRI gradient hardware, thereby reducing
the effect of field inhomogeneities,motion,and eddy currents. It helps
decrease scan time while respecting safety constraints.Acknowledgements
No acknowledgement found.References
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