Acquisition Strategies: Improving the Old & Exploring the New
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Wednesday May 11th
Room 513A-D |
10:30 - 12:30 |
Moderators: |
Michael Garwood and
Peter Jakob |
10:30 |
378. |
The "Central Signal
Singularity" Phenomenon in Balanced SSFP
R. Reeve Ingle1, and Dwight G. Nishimura1
1Electrical Engineering, Stanford University,
Stanford, California, United States
We investigate a phenomenon whereby small, alternating
perturbations of parameters (such as RF flip angles or
phases) in a balanced SSFP sequence can cause large,
localized deviations in the steady-state magnetization
profile. These deviations can be very severe (e.g.,
sharp notches or spikes in the magnetization profile)
but localized to a narrow range of off-resonant
frequencies, with the rest of the profile being
essentially identical to the unperturbed bSSFP profile.
We develop mathematical and physical explanations of
this phenomenon, demonstrate via Bloch simulations,
present phantom results, and describe potential
applications for positive-contrast imaging and fMRI.
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10:42 |
379. |
Desperately Seeking:
Non-Balanced Steady State Free Precession Fluid Signal
Oliver Bieri1, Carl Ganter2, and
Klaus Scheffler1
1Department of Medical Radiology,
Radiological Physics, University of Basel Hospital,
Basel, Switzerland, 2Institut
für Radiologie, Klinikum rechts der Isar, Technische
Universität München
Musculoskeletal (MSK) imaging benefits from increased
resolution at higher fields, as this may improve
diagnostic accuracy and confidence. Especially 3D double
echo steady state (DESS) sequences, offering a high
contrast between cartilage and joint fluid, have gained
increased interest for high resolution MSK imaging.
Here, we resolve the reason for a prominent loss of
contrast between fluid and tissues, as observed with
high resolution DESS imaging, but being inherent in all
non-balanced SSFP sequences. We will show that for
anisotropic scans the contrast between fluids and
tissues can be almost completely restored using an
alternative dephasing concept for non-balanced SSFP.
|
10:54 |
380. |
Fast Quantitative Double
Echo Steady State Diffusion Imaging
Oliver Bieri1, Carl Ganter2, and
Klaus Scheffler1
1Department of Medical Radiology,
Radiological Physics, University of Basel Hospital,
Basel, Switzerland, 2Institut
für Radiologie, Klinikum rechts der Isar, Technische
Universität München, Munich, Germany
In this work, a new and truly diffusion-weighted (i.e.,
relaxation time independent) SSFP technique is
introduced using a double-echo steady state approach
(true-dwDESS). As a result, quantitative SSFP DWI can be
performed in the very-rapid-pulsing regime which offers
substantially increased SNR and scanning efficiency.
Finally, high-resolution quantitative DWI is
demonstrated for human articular cartilage in the knee
joint at 3.0T.
|
11:06 |
381. |
Isotropic Mapping of T1,
T2, and M0 with
MP-DESS and Phase-Graph Data Fitting
Tony Stoecker1, Kaveh Vahedipour1,
Eberhard Pracht1, Daniel Brenner1,
and N. Jon Shah1,2
1Institute of Neuroscience and Medicine - 4,
Forschungszentrum Juelich, Juelich, Germany, 2Department
of Neurology, Faculty of Medicine, JARA, RWTH Aachen
University, Aachen, Germany
Mapping of relaxation times and proton density with high
isotropic resolution is best performed with a 3D
acquisition and, thus, short TR. As refocusing of
transverse magnetization is unavoidable in such
approaches, accurate quantification needs a signal
equation accounting for T2. Here, the DESS
sequence was chosen, where every Nth pulse was replaced
by a 180° magnetization preparation pulse (MP-DESS). The
echoes between two MP-pulses are segmented into several
images along the recovery. A proper signal equation is
given by the extended phase graph. The resulting
least-squares fit yields accurate T1, T2,
and M0 maps
in vivo.
|
11:18 |
382. |
Continuous SWIFT
Djaudat Idiyatullin1, Steven Suddarth2,
Curt Corum1, Gregor Adriany1, and
Michael Garwood1
1CMRR, Radiology, University of Minnesota,
Minneapolis, MN, United States, 2Agilent
Technologies, Santa Clara, CA, United States
This work describes the first attempt to implement SWIFT
(SWeep Imaging with Fourier Transform) in a continuous
mode for imaging and spectroscopy. We connected a
standard quadrature hybrid with quad coils and acquired
NMR signal during continuous radiofrequency excitation.
We utilized a chirped radiofrequency to minimize the
radiofrequency field for excitation of the spin system
for the target flip angle and bandwidth. Due to the
complete absence of “dead time” continuous SWIFT extends
the application of MRI and spectroscopy to studying spin
systems having extremely fast relaxation or broad
chemical shift distribution beyond that of the gapped
SWIFT sequence.
|
11:30 |
383. |
Interferometric Techniques
for Magnetic Resonance Imaging
Kenneth Otho Johnson1, and Craig H Meyer1
1Biomedical Engineering, University of
Virginia, Charlottesville, VA, United States
Interferometric techniques are developed for MR imaging.
Cross correlation of spectroscopic readouts provides
enhanced resolution to CSI, and may require fewer
readouts. A preliminary study illustrates the enhanced
resolution. The application of interferometric
techniques may have a broader impact on the MRI
community.
|
11:42 |
384. |
Self-Navigated Kinematic
Imaging of the Knee
Liheng Guo1, Antonio J Machado Segundo2,
John A Derbyshire3, John A Carrino2,
and Daniel A Herzka4
1Biomedical Engineering, Johns Hopkins
University, Baltimore, MD, United States, 2Department
of Radiology and Radiological Science, Johns Hopkins
School of Medicine,3Translational Medicine
Branch, DIR, NHLBI, National Institutes of Health,
Bethesda, MD, 41Department
of Biomedical Engineering, Johns Hopkins School of
Medicine
We propose a self-gated imaging method using navigator
projections acquired at high spatiotemporal resolution
and gated retrospective reconstruction, with the aim to
provide high-quality kinematic joint imaging with
minimal patient setup and no mechanical apparatus.
Preliminary 2D imaging results of the knee in 3T have
shown that the joint in motion can be clearly visualized
from the automatically reconstructed cine.
|
11:54 |
385. |
Spatial Selection Through
Multi-Coil Magnetic Field Shaping
Christoph Juchem1, Terence W Nixon1,
Peter B Brown1, Scott McIntyre1,
Douglas L Rothman1, and Robin A de Graaf1
1MR Research Center, Yale University, New
Haven, CT, United States
Magnetic field modeling with the multi-coil approach has
been used to generate anatomy-matched magnetic field
shapes that are spatially specific enough for the
selective excitation of individual regions in
2-dimensional slices with single frequency-selective RF
pulses. The low SAR method is demonstrated for brain
extraction and outer-volume-suppression (i.e. excitation
of everything but the brain) in the mouse at 9.4 Tesla.
|
12:06 |
386. |
SNR-Optimized Accelerated
Phase-Sensitive Dual-Acquisition Signle-Slab 3D Turbo Spin
Echo Imaging
Hyunyeol Lee1, Jin-Seok Seo1,2,
and Jaeseok Park2
1Department of Medical Science, Yonsei
University, Seoul, Korea, Republic of, 2Department
of Radiology, Yonsei University, Seoul, Korea, Republic
of
The proposed SNR optimized, accelerated,
phase-sensitive, dual-acquisition, single-slab, 3D,
turbo/fast spin echo imaging method simultaneously
enhances SNR and imaging efficiency by an optimal design
of variable refocusing flip angles in the second
acquisition period and elliptical incoherent sampling
patterns, while simultaneously generating high
resolution, isotropic, T2-weighted and CSF-suppressed
images within clinically acceptable imaging time
(~7mins).
|
12:18 |
387. |
3D radial bUTE
Clemens Diwoky1, and Rudolf Stollberger1
1Institute of Medical Engineering, Graz
University of Technology, Graz, Austria
Fully balanced steady state free precession (bSSFP)
acquisitions are known as the most efficient pulse
sequences in the perspective of SNR per time. For
high-field systems with higher resonance offsets and for
imaging parameters resulting in longer repetition times
the applicability of bSSFP is limited by banding
artefacts. To overcome or improve this limitation we
propose a balanced 3D-radial UTE sequence. The power of
this new approach could be shown with in-vivo high
resolution 3D imaging with 0.2 mm isotropic voxels on a
clinical 3T system in 7min.
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