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Improved myocardial scar visualization with fast free-breathing motion-compensated black-blood T1-rho-prepared late gadolinium enhancement MRI - 29/11/22

Doi : 10.1016/j.diii.2022.07.003 
Soumaya Sridi a, , Marta Nuñez-Garcia b, Maxime Sermesant b, c, Aurélien Maillot b, Dounia El Hamrani b, Julie Magat b, Jérôme Naulin b, François Laurent a, Michel Montaudon a, Pierre Jaïs b, d, Matthias Stuber b, e, f, Hubert Cochet a, b, Aurélien Bustin a, b, e
a Department of Cardiovascular Imaging, Groupe Hospitalier Sud, CHU Bordeaux, 33000, Pessac, France 
b IHU LIRYC, Electrophysiology and Heart Modeling Institute, Université de Bordeaux, INSERM U1045, 33600, Pessac, France 
c INRIA, Université Côte d'Azur, Sophia Antipolis, 06902, Valbonne, France 
d Department of Cardiac Electrophysiologhy, Hôpital Cardiologique du Haut-Lévêque, CHU de Bordeaux, 33600, Pessac, France 
e Department of Diagnostic and Interventional Radiology, Lausanne University Hospital and University of Lausanne, 1011, Lausanne, Switzerland 
f Center for Biomedical Imaging (CIBM), 1015, Lausanne, Switzerland 

Corresponding author.

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Highlights

Free-breathing black-blood late gadolinium enhancement cardiac MR images can be acquired in less than 2 min.
Non-rigid motion-compensated reconstruction enables free-breathing black-blood late gadolinium enhancement cardiac MR imaging.
Free-breathing black-blood late gadolinium enhancement cardiac MR imaging allows for improved detection of myocardial injuries.

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Abstract

Purpose

Clinical guidelines recommend the use of bright-blood late gadolinium enhancement (BR-LGE) for the detection and quantification of regional myocardial fibrosis and scar. This technique, however, may suffer from poor contrast at the blood-scar interface, particularly in patients with subendocardial myocardial infarction. The purpose of this study was to assess the clinical performance of a two-dimensional black-blood LGE (BL-LGE) sequence, which combines free-breathing T1-rho-prepared single-shot acquisitions with an advanced non-rigid motion-compensated patch-based reconstruction.

Materials and methods

Extended phase graph simulations and phantom experiments were performed to investigate the performance of the motion-correction algorithm and to assess the black-blood properties of the proposed sequence. Fifty-one patients (37 men, 14 women; mean age, 55 ± 15 [SD] years; age range: 19–81 years) with known or suspected cardiac disease prospectively underwent free-breathing T1-rho-prepared BL-LGE imaging with inline non-rigid motion-compensated patch-based reconstruction at 1.5T. Conventional breath-held BR-LGE images were acquired for comparison purposes. Acquisition times were recorded. Two readers graded the image quality and relative contrasts were calculated. Presence, location, and extent of LGE were evaluated.

Results

BL-LGE images were acquired with full ventricular coverage in 115 ± 25 (SD) sec (range: 64–160 sec). Image quality was significantly higher on free-breathing BL-LGE imaging than on its breath-held BR-LGE counterpart (3.6 ± 0.7 [SD] [range: 2–4] vs. 3.9 ± 0.2 [SD] [range: 3–4]) (P <0.01) and was graded as diagnostic for 44/51 (86%) patients. The mean scar-to-myocardium and scar-to-blood relative contrasts were significantly higher on BL-LGE images (P < 0.01 for both). The extent of LGE was larger on BL-LGE (median, 5 segments [IQR: 2, 7 segments] vs. median, 4 segments [IQR: 1, 6 segments]) (P < 0.01), the method being particularly sensitive in segments with LGE involving the subendocardium or papillary muscles. In eight patients (16%), BL-LGE could ascertain or rule out a diagnosis otherwise inconclusive on BR-LGE.

Conclusion

Free-breathing T1-rho-prepared BL-LGE imaging with inline motion compensated reconstruction offers a promising diagnostic technology for the non-invasive assessment of myocardial injuries.

Il testo completo di questo articolo è disponibile in PDF.

Keywords : Gadolinium enhancement, Heart, Magnetic resonance imaging, Myocardial infarction, Motion

Abbreviations : 2D, 3D, ADMM, BR-LGE, BL-LGE, bSSFP, CMR, ECG, FIDDLE, FSL, GMD, IQR, NGS, ROI, SD, SI, SL, T1ρ, TI, TSL


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© 2022  The Author(s). Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 103 - N° 12

P. 607-617 - dicembre 2022 Ritorno al numero
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