Methods for robust diffusion weighted body magnetic resonance imaging

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Abstract/Contents

Abstract
Diffusion weighted (DW) imaging is an increasingly common Magnetic Resonance Imaging (MRI) contrast in the clinic. There are several clinical applications that do not yet benefit from diffusion weighted imaging, owing to image artifacts encountered by conventional diffusion acquisitions. DW Fast Spin Echo (FSE) sequences are robust to field non-uniformities, but the non Carr-Purcell-Meiboom-Gill (CPMG) artifact must be addressed. Two different novel imaging reconstructions that can be applied to address the non CPMG artifact, were developed. The first reconstruction leverages calibrationless imaging and compressed sensing ideals to reduce the effect of T2 blur using shot locally low rank regularization. Combined with a diffusion prepared stimulated echo FSE sequence, it is shown to have reduced image distortion compared to conventional multi-shot DW-EPI techniques, and improved apparent resolution compared to vendor provided distortionless DW-FSE PROPELLER. The second reconstruction is a joint linear reconstruction for multi-shot quadratic phase increment data that can be acquired without a signal penalty. This reconstruction corrects ghosting artifacts from both shot-to-shot phase and intra-shot signal oscillations. A thorough analysis on the condition number of the proposed linear system shows that the conditioning is the same as applying parallel imaging to each shot, in the worst case, and the same as a standard multi-shot reconstruction in the best case. A clinically feasible sequence that achieves DW imaging near metal with moderate b-values and volumetric coverage in clinically feasible scan times, using diffusion-prepared FSE, was developed. Application of root-flipped Shinnar-Le Roux refocusing pulses permits preparation of a high spectral bandwidth, which improves imaging times by reducing the number of excitations required to cover the desired spectral range. B1 sensitivity is reduced by employing an excitation that satisfies the CPMG condition in the preparation. The gradient waveform used for ADC quantification was shown theoretically and experimentally to be insensitive to background gradients. Application in vivo demonstrates complementary contrast to conventional multispectral acquisitions and improved visualization compared to DW-EPI. Finally, a computationally efficient tool for optimizing the Cramér-Rao Lower Bound (CRLB) of quantitative sequences without using approximations or an analytical expression of the signal was developed. Automatic differentiation was applied to Bloch simulations and used to optimize several quantitative sequences without the need for approximations or an analytical expression. The results were validated with in vivo measurements and comparisons to prior art. The CRLB of the Magnetic Resonance Fingerprinting (MRF) sequence, which has a complicated analytical formulation, was optimized using automatic differentiation.

Description

Type of resource text
Form electronic resource; remote; computer; online resource
Extent 1 online resource.
Place California
Place [Stanford, California]
Publisher [Stanford University]
Copyright date 2022; ©2022
Publication date 2022; 2022
Issuance monographic
Language English

Creators/Contributors

Author Lee, Philip Kenneth
Degree supervisor Hargreaves, Brian Andrew
Thesis advisor Hargreaves, Brian Andrew
Thesis advisor Nishimura, Dwight George
Thesis advisor Pauly, John (John M.)
Degree committee member Nishimura, Dwight George
Degree committee member Pauly, John (John M.)
Associated with Stanford University, Department of Electrical Engineering

Subjects

Genre Theses
Genre Text

Bibliographic information

Statement of responsibility Philip Kenneth Lee.
Note Submitted to the Department of Electrical Engineering.
Thesis Thesis Ph.D. Stanford University 2022.
Location https://purl.stanford.edu/cw045gq7614

Access conditions

Copyright
© 2022 by Philip Kenneth Lee
License
This work is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported license (CC BY-NC).

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