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Three‐directional acceleration phase mapping of myocardial function

An optimized acceleration encoded phase contrast method termed “acceleration phase mapping” for the assessment of regional myocardial function is presented. Based on an efficient gradient waveform design using two‐sided encoding for in vivo three‐directional acceleration mapping, echo and repetition...

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Bibliographic Details
Published in:Magnetic resonance in medicine 2011-05, Vol.65 (5), p.1335-1345
Main Authors: Staehle, Felix, Jung, Bernd A., Bauer, Simon, Leupold, Jochen, Bock, Jelena, Lorenz, Ramona, Föll, Daniela, Markl, Michael
Format: Article
Language:English
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Summary:An optimized acceleration encoded phase contrast method termed “acceleration phase mapping” for the assessment of regional myocardial function is presented. Based on an efficient gradient waveform design using two‐sided encoding for in vivo three‐directional acceleration mapping, echo and repetition times TE = 12–14 ms and TR = 15–17 ms for low accelerations sensitivity aenc = 5–8 m/s2 were achieved. In addition to phantom validation, the technique was applied in a study with 10 healthy volunteers at 1.5T and 3T to evaluate its feasibility to assess regional myocardial acceleration at 1.5T and 3T. Results of the acceleration measurements were compared with the temporal derivative of myocardial velocities from three‐directional velocity encoded standard phase contrast MRI in the same volunteers. The feasibility to assess myocardial acceleration along the radial, circumferential, and longitudinal direction of the left ventricle was demonstrated. Despite improved signal‐to‐noise‐ratio at 3T (34% increase compared with 1.5T), image quality with respect to susceptibility artifacts was better 1.5T compared with 3T. Analysis of global and regional left ventricular acceleration showed characteristic patterns of systolic and diastolic acceleration and deceleration. Comparisons of directly measured and derived myocardial acceleration dynamics over the cardiac cycle revealed good correlation (r = 0.45–0.68, P < 0.01) between both methods. Magn Reson Med, 2011. © 2011 Wiley‐Liss, Inc.
ISSN:0740-3194
1522-2594
1522-2594
DOI:10.1002/mrm.22744