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Radiofrequency antenna concepts for human cardiac MR at 14.0 T

OBJECTIVE: To examine the feasibility of human cardiac MR (CMR) at 14.0 T using high-density radiofrequency (RF) dipole transceiver arrays in conjunction with static and dynamic parallel transmission (pTx). MATERIALS AND METHODS: RF arrays comprised of self-grounded bow-tie (SGBT) antennas, bow-tie...

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Autores principales: Nurzed, Bilguun, Kuehne, Andre, Aigner, Christoph Stefan, Schmitter, Sebastian, Niendorf, Thoralf, Eigentler, Thomas Wilhelm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140016/
https://www.ncbi.nlm.nih.gov/pubmed/36920549
http://dx.doi.org/10.1007/s10334-023-01075-1
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author Nurzed, Bilguun
Kuehne, Andre
Aigner, Christoph Stefan
Schmitter, Sebastian
Niendorf, Thoralf
Eigentler, Thomas Wilhelm
author_facet Nurzed, Bilguun
Kuehne, Andre
Aigner, Christoph Stefan
Schmitter, Sebastian
Niendorf, Thoralf
Eigentler, Thomas Wilhelm
author_sort Nurzed, Bilguun
collection PubMed
description OBJECTIVE: To examine the feasibility of human cardiac MR (CMR) at 14.0 T using high-density radiofrequency (RF) dipole transceiver arrays in conjunction with static and dynamic parallel transmission (pTx). MATERIALS AND METHODS: RF arrays comprised of self-grounded bow-tie (SGBT) antennas, bow-tie (BT) antennas, or fractionated dipole (FD) antennas were used in this simulation study. Static and dynamic pTx were applied to enhance transmission field (B(1)(+)) uniformity and efficiency in the heart of the human voxel model. B(1)(+) distribution and maximum specific absorption rate averaged over 10 g tissue (SAR(10g)) were examined at 7.0 T and 14.0 T. RESULTS: At 14.0 T static pTx revealed a minimum B(1)(+)(ROI) efficiency of 0.91 μT/√kW (SGBT), 0.73 μT/√kW (BT), and 0.56 μT/√kW (FD) and maximum SAR(10g) of 4.24 W/kg, 1.45 W/kg, and 2.04 W/kg. Dynamic pTx with 8 kT points indicate a balance between B(1)(+)(ROI) homogeneity (coefficient of variation < 14%) and efficiency (minimum B(1)(+)(ROI) > 1.11 µT/√kW) at 14.0 T with a maximum SAR(10g) < 5.25 W/kg. DISCUSSION: MRI of the human heart at 14.0 T is feasible from an electrodynamic and theoretical standpoint, provided that multi-channel high-density antennas are arranged accordingly. These findings provide a technical foundation for further explorations into CMR at 14.0 T. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10334-023-01075-1.
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spelling pubmed-101400162023-04-29 Radiofrequency antenna concepts for human cardiac MR at 14.0 T Nurzed, Bilguun Kuehne, Andre Aigner, Christoph Stefan Schmitter, Sebastian Niendorf, Thoralf Eigentler, Thomas Wilhelm MAGMA Research Article OBJECTIVE: To examine the feasibility of human cardiac MR (CMR) at 14.0 T using high-density radiofrequency (RF) dipole transceiver arrays in conjunction with static and dynamic parallel transmission (pTx). MATERIALS AND METHODS: RF arrays comprised of self-grounded bow-tie (SGBT) antennas, bow-tie (BT) antennas, or fractionated dipole (FD) antennas were used in this simulation study. Static and dynamic pTx were applied to enhance transmission field (B(1)(+)) uniformity and efficiency in the heart of the human voxel model. B(1)(+) distribution and maximum specific absorption rate averaged over 10 g tissue (SAR(10g)) were examined at 7.0 T and 14.0 T. RESULTS: At 14.0 T static pTx revealed a minimum B(1)(+)(ROI) efficiency of 0.91 μT/√kW (SGBT), 0.73 μT/√kW (BT), and 0.56 μT/√kW (FD) and maximum SAR(10g) of 4.24 W/kg, 1.45 W/kg, and 2.04 W/kg. Dynamic pTx with 8 kT points indicate a balance between B(1)(+)(ROI) homogeneity (coefficient of variation < 14%) and efficiency (minimum B(1)(+)(ROI) > 1.11 µT/√kW) at 14.0 T with a maximum SAR(10g) < 5.25 W/kg. DISCUSSION: MRI of the human heart at 14.0 T is feasible from an electrodynamic and theoretical standpoint, provided that multi-channel high-density antennas are arranged accordingly. These findings provide a technical foundation for further explorations into CMR at 14.0 T. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10334-023-01075-1. Springer International Publishing 2023-03-15 2023 /pmc/articles/PMC10140016/ /pubmed/36920549 http://dx.doi.org/10.1007/s10334-023-01075-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Nurzed, Bilguun
Kuehne, Andre
Aigner, Christoph Stefan
Schmitter, Sebastian
Niendorf, Thoralf
Eigentler, Thomas Wilhelm
Radiofrequency antenna concepts for human cardiac MR at 14.0 T
title Radiofrequency antenna concepts for human cardiac MR at 14.0 T
title_full Radiofrequency antenna concepts for human cardiac MR at 14.0 T
title_fullStr Radiofrequency antenna concepts for human cardiac MR at 14.0 T
title_full_unstemmed Radiofrequency antenna concepts for human cardiac MR at 14.0 T
title_short Radiofrequency antenna concepts for human cardiac MR at 14.0 T
title_sort radiofrequency antenna concepts for human cardiac mr at 14.0 t
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140016/
https://www.ncbi.nlm.nih.gov/pubmed/36920549
http://dx.doi.org/10.1007/s10334-023-01075-1
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