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Accelerating Brain Imaging Using a Silent Spatial Encoding Axis
PURPOSE: To characterize the acceleration capabilities of a silent head insert gradient axis that operates at the inaudible frequency of 20 kHz and a maximum gradient amplitude of 40 mT/m without inducing peripheral nerve stimulation. METHODS: The silent gradient axis' acquisitions feature an o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544176/ https://www.ncbi.nlm.nih.gov/pubmed/35696540 http://dx.doi.org/10.1002/mrm.29350 |
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author | Versteeg, Edwin Klomp, Dennis W. J. Siero, Jeroen C. W. |
author_facet | Versteeg, Edwin Klomp, Dennis W. J. Siero, Jeroen C. W. |
author_sort | Versteeg, Edwin |
collection | PubMed |
description | PURPOSE: To characterize the acceleration capabilities of a silent head insert gradient axis that operates at the inaudible frequency of 20 kHz and a maximum gradient amplitude of 40 mT/m without inducing peripheral nerve stimulation. METHODS: The silent gradient axis' acquisitions feature an oscillating gradient in the phase‐encoding direction that is played out on top of a cartesian readout, similarly as done in Wave‐CAIPI. The additional spatial encoding fills k‐space in readout lanes allowing for the acquisition of fewer phase‐encoding steps without increasing aliasing artifacts. Fully sampled 2D gradient echo datasets were acquired both with and without the silent readout. All scans were retrospectively undersampled (acceleration factors R = 1 to 12) to compare conventional SENSE acceleration and acceleration using the silent gradient. The silent gradient amplitude and the readout bandwidth were varied to investigate the effect on artifacts and g‐factor. RESULTS: The silent readout reduced the g‐factor for all acceleration factors when compared to SENSE acceleration. Increasing the silent gradient amplitude from 31.5 mT/m to 40 mT/m at an acceleration factor of 10 yielded a reduction in the average g‐factor (g(avg)) from 1.3 ± 0.14 (g(max) = 1.9) to 1.1 ± 0.09 (g(max) = 1.6)(.) Furthermore, reducing the number of cycles increased the readout bandwidth and the g‐factor that reached g(avg) = 1.5 ± 0.16 for a readout bandwidth of 651 Hz/pixel and an acceleration factor of R = 8. CONCLUSION: A silent gradient axis enables high acceleration factors up to R = 10 while maintaining a g‐factor close to unity (g(avg) = 1.1 and g(max) = 1.6) and can be acquired with clinically relevant readout bandwidths. |
format | Online Article Text |
id | pubmed-9544176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95441762022-10-14 Accelerating Brain Imaging Using a Silent Spatial Encoding Axis Versteeg, Edwin Klomp, Dennis W. J. Siero, Jeroen C. W. Magn Reson Med Technical Notes–Imaging Methodology PURPOSE: To characterize the acceleration capabilities of a silent head insert gradient axis that operates at the inaudible frequency of 20 kHz and a maximum gradient amplitude of 40 mT/m without inducing peripheral nerve stimulation. METHODS: The silent gradient axis' acquisitions feature an oscillating gradient in the phase‐encoding direction that is played out on top of a cartesian readout, similarly as done in Wave‐CAIPI. The additional spatial encoding fills k‐space in readout lanes allowing for the acquisition of fewer phase‐encoding steps without increasing aliasing artifacts. Fully sampled 2D gradient echo datasets were acquired both with and without the silent readout. All scans were retrospectively undersampled (acceleration factors R = 1 to 12) to compare conventional SENSE acceleration and acceleration using the silent gradient. The silent gradient amplitude and the readout bandwidth were varied to investigate the effect on artifacts and g‐factor. RESULTS: The silent readout reduced the g‐factor for all acceleration factors when compared to SENSE acceleration. Increasing the silent gradient amplitude from 31.5 mT/m to 40 mT/m at an acceleration factor of 10 yielded a reduction in the average g‐factor (g(avg)) from 1.3 ± 0.14 (g(max) = 1.9) to 1.1 ± 0.09 (g(max) = 1.6)(.) Furthermore, reducing the number of cycles increased the readout bandwidth and the g‐factor that reached g(avg) = 1.5 ± 0.16 for a readout bandwidth of 651 Hz/pixel and an acceleration factor of R = 8. CONCLUSION: A silent gradient axis enables high acceleration factors up to R = 10 while maintaining a g‐factor close to unity (g(avg) = 1.1 and g(max) = 1.6) and can be acquired with clinically relevant readout bandwidths. John Wiley and Sons Inc. 2022-06-13 2022-10 /pmc/articles/PMC9544176/ /pubmed/35696540 http://dx.doi.org/10.1002/mrm.29350 Text en © 2022 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals LLC on behalf of International Society for Magnetic Resonance in Medicine. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Technical Notes–Imaging Methodology Versteeg, Edwin Klomp, Dennis W. J. Siero, Jeroen C. W. Accelerating Brain Imaging Using a Silent Spatial Encoding Axis |
title | Accelerating Brain Imaging Using a Silent Spatial Encoding Axis |
title_full | Accelerating Brain Imaging Using a Silent Spatial Encoding Axis |
title_fullStr | Accelerating Brain Imaging Using a Silent Spatial Encoding Axis |
title_full_unstemmed | Accelerating Brain Imaging Using a Silent Spatial Encoding Axis |
title_short | Accelerating Brain Imaging Using a Silent Spatial Encoding Axis |
title_sort | accelerating brain imaging using a silent spatial encoding axis |
topic | Technical Notes–Imaging Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544176/ https://www.ncbi.nlm.nih.gov/pubmed/35696540 http://dx.doi.org/10.1002/mrm.29350 |
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