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Poster Sessions<br />

1627. A Novel Robust Algorithm to Correct for Eddy Current Distortions in High B-Value Diffusion MRI<br />

Henrik Hansson 1 , Jimmy Lätt, 12 , Freddy Ståhlberg 1,3 , Markus Nilsson 1<br />

1 Department of Medical Radiation Physics, Lund University, Lund, Sweden; 2 Center for Medical Imaging and Physiology, Lund<br />

University Hospital, Lund, Sweden; 3 Department of Diagnostic Radiology, Lund University, Lund, Sweden<br />

Eddy currents distort diffusion-weighted images, which give rise to artefacts in the estimated apparent diffusion coefficient and the diffusion kurtosis.<br />

Current correction methods are not effective for b-values greater than 1000 s/mm2. We have developed a correction algorithm based on comparison of all<br />

images in an image set, instead of separate volumes. This allows model based distortion correction by maximizing the local correlation of the entire image<br />

set.<br />

1628. Rapid Automated QA for Diffusion MRI<br />

Adriaan L. Moerland 1 , Elizabeth A. Moore 2<br />

1 Advanced Development, Philips Healthcare BV, Best, Netherlands; 2 MR Clinical Science, Philips Healthcare BV, Best, Netherlands<br />

Diffusion MRI is increasingly important in clinical radiology, however the technique is very sensitive to system defects in the gradient chain. A new method<br />

has been developed for easy QA in diffusion MRI. The acquisition is 3 fast DTI scans on a spherical aqueous phantom, taking less than 3 minutes. Analysis<br />

is fully automated and derives measures of deformation of the circular phantom image as well as apparent diffusion coefficient ADC and fractional<br />

anisotropy FA values. Two of the deformation measures were found to be highly sensitive to gradient defects such as eddy current (mis)calibration.<br />

1629. Optimizing Accuracy and Precision in High Resolution Diffusion Tensor Imaging of the Ex Vivo Rat<br />

Heart<br />

Patrick William Hales 1 , Rebecca Burton 2 , Christian Bollensdorff 2 , Jurgen E. Schneider 1<br />

1 Cardiovascular Medicine, Oxford University, Oxford, Oxon, United Kingdom; 2 Physiology, Anatomy & Genetics, Oxford<br />

University, Oxford, Oxon, United Kingdom<br />

The influence of both SNR and diffusion gradient sampling scheme on the precision and accuracy of high resolution (203 μm) DTI data acquired in the ex<br />

vivo rat heart has been investigated. We demonstrate how the use of reduced encoding of diffusion weighted images using the approximate generalized<br />

series reconstruction technique can increase SNR without increasing scan time, and how this can be employed to reduce the overall error in the primary<br />

eigenvector orientation.<br />

1630. About the Origins of Diffusion-Weighting Due to the Non-Linear Phase Dispersion Induced by<br />

Frequency-Swept Pulses<br />

Julien Valette 1,2 , Denis Le Bihan 2 , Franck Lethimonnier 2<br />

1 CEA-MIRCen, Fontenay-aux-Roses, France; 2 CEA-NeuroSpin, Gif-sur-Yvette, France<br />

It has been recognized in the past that the non-linear phase induced by frequency-swept pulses may cause diffusion-weighting. In the present work, the<br />

origins of the non-linear phase dispersion induced by frequency-swept pulses are revisited, in order to assess whether the phase variation of the B1 field<br />

during the sweep should be explicitly considered when calculating diffusion weighting. Following this analysis, an analytical expression is derived for<br />

diffusion-weighting induced by a pair of slice selective hyperbolic secant pulses, and confronted to numerical simulation of the Bloch equations including<br />

diffusion.<br />

1631. On the Accuracy of Diffusion Models for Fast Low-Angle Short-TR SSFP-Echo (FLASH-DW SSFP)<br />

Oliver Bieri 1 , Carl Ganter 2 , Klaus Scheffler 1<br />

1 Radiological Physics, University of Basel Hospital, Basel, Switzerland; 2 Department of Diagnostic Radiology, Technical University<br />

Munich, Munich, Germany<br />

Several models have been developed for the description of diffusion in steady-state free precession (SSFP) sequences. For clinical practice, high SNR and<br />

short acquisition times are desirable with DW-SSFP. In this work, a new approach for quantitative diffusion imaging is proposed using a fast low-angle<br />

short-TR (FLASH) diffusion-weighted (DW) SSFP sequence. The accuracy of diffusion models is assed in-vitro and the feasibility of high resolution<br />

quantitative diffusion mapping is demonstrated in-vivo for human articular cartilage.<br />

1632. Simultaneously Measuring Axonal Diameter Distribution and Direction of Rat Brain Using Q-Space<br />

Diffusion Tensor Magnetic Resonance Imaging<br />

Jun-Cheng Weng 1<br />

1 Department of Medical Imaging and Radiological Sciences, Chung Shan Medical University, Taichung, Taiwan<br />

Fundamental relationships between diffusion tensor imaging (DTI) and q-space imaging can be derived which establish conditions when these two<br />

complementary MR methods are equivalent. When the 3D displacement distribution is measured by q-space imaging with large displacement and small q<br />

vector, the result is similar to 3D Gaussian assumed in DTI. Combing displacement information from q-space imaging and fiber direction from DTI,<br />

distribution of axonal diameters and directions could be derived at the same time. The study proposed a novel technique, q-space diffusion tensor imaging<br />

(qDTI), combined with two image reconstruction methods based on the assumption to simultaneously map axonal diameter distribution and direction of rat<br />

brain. One was tensor-based method. The 3D Gaussian displacement distribution could be obtained directly by the displacement tensor. The other was<br />

displacement projection method. The effective axonal diameter was defined as the average of several displacements projected to the direction of the fiber<br />

section. They provided MR images in which physical parameters of water diffusion such as the mean displacement and maximum diffusivity of water<br />

molecules were used as image contrast. Our results demonstrated that two qDTI methods both produced reasonable distribution of effective axonal diameters<br />

and directions in rat brain.

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