The strong sensitivity of Carr-Purcell-Meiboom-Gill (CPMG) fast spin-echo (FSE) sequences, such as rapid acquisition with relaxation enhancement (RARE), to the phase of the prepared transverse magnetization means that artifact-free single-shot diffusion-weighted images can currently only be obtained
Single-shot diffusion MRI of human brain on a conventional clinical instrument
✍ Scribed by Guoying Liu; Peter Van Gelderen; Jeff Duyn; Chrit T. W. Moonen
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 789 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A single‐shot diffusion MRI technique on a standard clinical 1.5T scanner is presented. The method incorporates the following elements: (a) an inversion RF pulse followed by a delay of 1.3 s to null cerebral spinal fluid (CSF) signal, (b) a stimulated echo sequence (TE=56 ms, TM=100 ms) to obtain strong diffusion weighting, (c) a single‐shot gradient‐ and spin‐echo (GRASE) sequence for imaging with a modified k‐space trajectory and Carr‐Purcell Meiboom‐Gill (CPMG)‐phase cycle. The trace of the diffusion coefficient obtained with this approach is in good agreement with values reported for animal brain, and for recent human studies. It is demonstrated that single‐shot diffusion imaging of human brain is feasible on an unmodified standard instrument without high‐gradient slew rate or extreme field homogeneity.
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