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High resolution diffusion‐weighted imaging using readout‐segmented echo‐planar imaging, parallel imaging and a two‐dimensional navigator‐based reacquisition
Author(s) -
Porter David A.,
Heidemann Robin M.
Publication year - 2009
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.22024
Subject(s) - echo planar imaging , artifact (error) , computer science , artificial intelligence , computer vision , single shot , diffusion mri , diffusion imaging , signal (programming language) , phase (matter) , sensitivity (control systems) , magnetic resonance imaging , physics , radiology , medicine , optics , quantum mechanics , electronic engineering , programming language , engineering
Single‐shot echo‐planar imaging (EPI) is well established as the method of choice for clinical, diffusion‐weighted imaging with MRI because of its low sensitivity to the motion‐induced phase errors that occur during diffusion sensitization of the MR signal. However, the method is prone to artifacts due to susceptibility changes at tissue interfaces and has a limited spatial resolution. The introduction of parallel imaging techniques, such as GRAPPA (GeneRalized Autocalibrating Partially Parallel Acquisitions), has reduced these problems, but there are still significant limitations, particularly at higher field strengths, such as 3 Tesla (T), which are increasingly being used for routine clinical imaging. This study describes how the combination of readout‐segmented EPI and parallel imaging can be used to address these issues by generating high‐resolution, diffusion‐weighted images at 1.5T and 3T with a significant reduction in susceptibility artifact compared with the single‐shot case. The technique uses data from a 2D navigator acquisition to perform a nonlinear phase correction and to control the real‐time reacquisition of unusable data that cannot be corrected. Measurements on healthy volunteers demonstrate that this approach provides a robust correction for motion‐induced phase artifact and allows scan times that are suitable for routine clinical application. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.