Robust phase unwrapping for MR temperature imaging using a magnitude-sorted list, multi-clustering algorithm

Purpose Several methods in MRI use the phase information of the complex signal and require phase unwrapping (e.g., B0 field mapping, chemical shift imaging, and velocity measurements). In this work, an algorithm was developed focusing on the needs and requirements of MR temperature imaging applicati...

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Published in:Magnetic resonance in medicine Vol. 73; no. 4; pp. 1662 - 1668
Main Authors: Maier, Florian, Fuentes, David, Weinberg, Jeffrey S., Hazle, John D., Stafford, R. Jason
Format: Journal Article
Language:English
Published: United States Blackwell Publishing Ltd 01-04-2015
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Summary:Purpose Several methods in MRI use the phase information of the complex signal and require phase unwrapping (e.g., B0 field mapping, chemical shift imaging, and velocity measurements). In this work, an algorithm was developed focusing on the needs and requirements of MR temperature imaging applications. Methods The proposed method performs fully automatic unwrapping using a list of all pixels sorted by magnitude in descending order and creates and merges clusters of unwrapped pixels until the entire image is unwrapped. The algorithm was evaluated using simulated phantom data and in vivo clinical temperature imaging data. Results The evaluation of the phantom data demonstrated no errors in regions with signal‐to‐noise ratios of at least 4.5. For the in vivo data, the algorithm did not fail at an average of more than one pixel for signal‐to‐noise ratios greater than 6.3. Processing times less than 30 ms per image were achieved by unwrapping pixels inside a region of interest (53 × 53 pixels) used for referenceless MR temperature imaging. Conclusions The algorithm has been demonstrated to operate robustly with clinical in vivo data in this study. The processing time for common regions of interest in referenceless MR temperature imaging allows for online updates of temperature maps without noticeable delay. Magn Reson Med 73:1662–1668, 2015. © 2014 Wiley Periodicals, Inc.
Bibliography:ArticleID:MRM25279
ark:/67375/WNG-3WBXBKFR-B
istex:46740E62AEDCA79F3E1E95E8DE3F4D31F4FA9353
NIH - No. CA79282; No. CA016672; No. 5T32CA119930-03; No. 1R21EB010196-01
Parts of this work were presented at the Annual Meeting of the ISMRM in 2013.
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ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.25279