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Validation of cardiac diffusion tensor imaging sequences: A multicentre test-retest phantom study.

Irvin TehWilliam A Romero RJordan BoyleJaume Coll-FontErica Dall'ArmellinaDaniel B EnnisPedro F FerreiraPrateek KalraArunark KolipakaSebastian KozerkeDavid LohrFrançois-Pierre MongeonKevin MoulinChristopher T NguyenSonia Nielles-VallespinBrian RatermanLaura Maria SchreiberAndrew D ScottDavid E SosnovikChristian T StoeckCyril TousElizabeth M TunnicliffeAndreas Max WengPierre CroisilleMagalie ViallonJurgen E Schneider
Published in: NMR in biomedicine (2022)
Cardiac diffusion tensor imaging (DTI) is an emerging technique for the in vivo characterisation of myocardial microstructure, and there is a growing need for its validation and standardisation. We sought to establish the accuracy, precision, repeatability and reproducibility of state-of-the-art pulse sequences for cardiac DTI among 10 centres internationally. Phantoms comprising 0%-20% polyvinylpyrrolidone (PVP) were scanned with DTI using a product pulsed gradient spin echo (PGSE; N = 10 sites) sequence, and a custom motion-compensated spin echo (SE; N = 5) or stimulated echo acquisition mode (STEAM; N = 5) sequence suitable for cardiac DTI in vivo. A second identical scan was performed 1-9 days later, and the data were analysed centrally. The average mean diffusivities (MDs) in 0% PVP were (1.124, 1.130, 1.113) x 10 -3  mm 2 /s for PGSE, SE and STEAM, respectively, and accurate to within 1.5% of reference data from the literature. The coefficients of variation in MDs across sites were 2.6%, 3.1% and 2.1% for PGSE, SE and STEAM, respectively, and were similar to previous studies using only PGSE. Reproducibility in MD was excellent, with mean differences in PGSE, SE and STEAM of (0.3 ± 2.3, 0.24 ± 0.95, 0.52 ± 0.58) x 10 -5  mm 2 /s (mean ± 1.96 SD). We show that custom sequences for cardiac DTI provide accurate, precise, repeatable and reproducible measurements. Further work in anisotropic and/or deforming phantoms is warranted.
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