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Three dimensional first-pass myocardial perfusion imaging at 3T: feasibility study
BACKGROUND: In patients with ischemic heart disease, accurate assessment of the extent of myocardial perfusion deficit may be important in predicting prognosis of clinical cardiac outcomes. The aim of this study was to compare the ability of three dimensional (3D) and of two dimensional (2D) multi-s...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614420/ https://www.ncbi.nlm.nih.gov/pubmed/19077220 http://dx.doi.org/10.1186/1532-429X-10-57 |
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author | Shin, Taehoon Hu, Houchun H Pohost, Gerald M Nayak, Krishna S |
author_facet | Shin, Taehoon Hu, Houchun H Pohost, Gerald M Nayak, Krishna S |
author_sort | Shin, Taehoon |
collection | PubMed |
description | BACKGROUND: In patients with ischemic heart disease, accurate assessment of the extent of myocardial perfusion deficit may be important in predicting prognosis of clinical cardiac outcomes. The aim of this study was to compare the ability of three dimensional (3D) and of two dimensional (2D) multi-slice myocardial perfusion imaging (MPI) using cardiovascular magnetic resonance (CMR) in determining the size of defects, and to demonstrate the feasibility of 3D MPI in healthy volunteers at 3 Tesla. METHODS: A heart phantom was used to compare the accuracy of 3D and 2D multi-slice MPI in estimating the volume fraction of seven rubber insets which simulated transmural myocardial perfusion defects. Three sets of cross-sectional planes were acquired for 2D multi-slice imaging, where each set was shifted along the partition encoding direction by ± 10 mm. 3D first-pass contrast-enhanced (0.1 mmol/kg Gd-DTPA) MPI was performed in three volunteers with sensitivity encoding for six-fold acceleration. The upslope of the myocardial time-intensity-curve and peak SNR/CNR values were calculated. RESULTS: Mean/standard deviation of errors in estimating the volume fraction across the seven defects were -0.44/1.49%, 2.23/2.97%, and 2.59/3.18% in 3D, 2D 4-slice, and 2D 3-slice imaging, respectively. 3D MPI performed in healthy volunteers produced excellent quality images with whole left ventricular (LV) coverage. Peak SNR/CNR was 57.6 ± 22.0/37.5 ± 19.7 over all segments in the first eight slices. CONCLUSION: 3D performed better than 2D multi-slice MPI in estimating the size of perfusion defects in phantoms. Highly accelerated 3D MPI at 3T was feasible in volunteers, allowing whole LV coverage with excellent image quality and high SNR/CNR. |
format | Text |
id | pubmed-2614420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26144202009-01-07 Three dimensional first-pass myocardial perfusion imaging at 3T: feasibility study Shin, Taehoon Hu, Houchun H Pohost, Gerald M Nayak, Krishna S J Cardiovasc Magn Reson Technical Notes BACKGROUND: In patients with ischemic heart disease, accurate assessment of the extent of myocardial perfusion deficit may be important in predicting prognosis of clinical cardiac outcomes. The aim of this study was to compare the ability of three dimensional (3D) and of two dimensional (2D) multi-slice myocardial perfusion imaging (MPI) using cardiovascular magnetic resonance (CMR) in determining the size of defects, and to demonstrate the feasibility of 3D MPI in healthy volunteers at 3 Tesla. METHODS: A heart phantom was used to compare the accuracy of 3D and 2D multi-slice MPI in estimating the volume fraction of seven rubber insets which simulated transmural myocardial perfusion defects. Three sets of cross-sectional planes were acquired for 2D multi-slice imaging, where each set was shifted along the partition encoding direction by ± 10 mm. 3D first-pass contrast-enhanced (0.1 mmol/kg Gd-DTPA) MPI was performed in three volunteers with sensitivity encoding for six-fold acceleration. The upslope of the myocardial time-intensity-curve and peak SNR/CNR values were calculated. RESULTS: Mean/standard deviation of errors in estimating the volume fraction across the seven defects were -0.44/1.49%, 2.23/2.97%, and 2.59/3.18% in 3D, 2D 4-slice, and 2D 3-slice imaging, respectively. 3D MPI performed in healthy volunteers produced excellent quality images with whole left ventricular (LV) coverage. Peak SNR/CNR was 57.6 ± 22.0/37.5 ± 19.7 over all segments in the first eight slices. CONCLUSION: 3D performed better than 2D multi-slice MPI in estimating the size of perfusion defects in phantoms. Highly accelerated 3D MPI at 3T was feasible in volunteers, allowing whole LV coverage with excellent image quality and high SNR/CNR. BioMed Central 2008-12-11 /pmc/articles/PMC2614420/ /pubmed/19077220 http://dx.doi.org/10.1186/1532-429X-10-57 Text en Copyright © 2008 Shin et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Technical Notes Shin, Taehoon Hu, Houchun H Pohost, Gerald M Nayak, Krishna S Three dimensional first-pass myocardial perfusion imaging at 3T: feasibility study |
title | Three dimensional first-pass myocardial perfusion imaging at 3T: feasibility study |
title_full | Three dimensional first-pass myocardial perfusion imaging at 3T: feasibility study |
title_fullStr | Three dimensional first-pass myocardial perfusion imaging at 3T: feasibility study |
title_full_unstemmed | Three dimensional first-pass myocardial perfusion imaging at 3T: feasibility study |
title_short | Three dimensional first-pass myocardial perfusion imaging at 3T: feasibility study |
title_sort | three dimensional first-pass myocardial perfusion imaging at 3t: feasibility study |
topic | Technical Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614420/ https://www.ncbi.nlm.nih.gov/pubmed/19077220 http://dx.doi.org/10.1186/1532-429X-10-57 |
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