Black-blood native T mapping: Blood signal suppression for reduced partial voluming in the myocardium.

Magn Reson Med

Computer Assisted Clinical Medicine, University Medical Center Mannheim, Heidelberg University, Mannheim, Germany.

Published: August 2017

Purpose: To study the feasibility of black-blood contrast in native T mapping for reduction of partial voluming at the blood-myocardium interface.

Methods: A saturation pulse prepared heart-rate-independent inversion recovery (SAPPHIRE) T mapping sequence was combined with motion-sensitized driven-equilibrium (MSDE) blood suppression for black-blood T mapping at 3 Tesla. Phantom scans were performed to assess the T time accuracy. In vivo black-blood and conventional SAPPHIRE T mapping was performed in eight healthy subjects and analyzed for T times, precision, and inter- and intraobserver variability. Furthermore, manually drawn regions of interest (ROIs) in all T maps were dilated and eroded to analyze the dependence of septal T times on the ROI thickness.

Results: Phantom results and in vivo myocardial T times show comparable accuracy with black-blood compared to conventional SAPPHIRE (in vivo: black-blood: 1562 ± 56 ms vs. conventional: 1583 ± 58 ms, P = 0.20); Using black-blood SAPPHIRE precision was significantly lower (standard deviation: 133.9 ± 24.6 ms vs. 63.1 ± 6.4 ms, P < .0001), and blood T time measurement was not possible. Significantly increased interobserver interclass correlation coefficient (ICC) (0.996 vs. 0.967, P = 0.011) and similar intraobserver ICC (0.979 vs. 0.939, P = 0.11) was obtained with the black-blood sequence. Conventional SAPPHIRE showed strong dependence on the ROI thickness (R = 0.99). No such trend was observed using the black-blood approach (R = 0.29).

Conclusion: Black-blood SAPPHIRE successfully eliminates partial voluming at the blood pool in native myocardial T mapping while providing accurate T times, albeit at a reduced precision. Magn Reson Med 78:484-493, 2017. © 2016 International Society for Magnetic Resonance in Medicine.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562488PMC
http://dx.doi.org/10.1002/mrm.26378DOI Listing

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