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4D deep learning for real-time volumetric optical coherence elastography
PURPOSE: Elasticity of soft tissue provides valuable information to physicians during treatment and diagnosis of diseases. A number of approaches have been proposed to estimate tissue stiffness from the shear wave velocity. Optical coherence elastography offers a particularly high spatial and tempor...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822782/ https://www.ncbi.nlm.nih.gov/pubmed/32997312 http://dx.doi.org/10.1007/s11548-020-02261-5 |
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author | Neidhardt, M. Bengs, M. Latus, S. Schlüter, M. Saathoff, T. Schlaefer, A. |
author_facet | Neidhardt, M. Bengs, M. Latus, S. Schlüter, M. Saathoff, T. Schlaefer, A. |
author_sort | Neidhardt, M. |
collection | PubMed |
description | PURPOSE: Elasticity of soft tissue provides valuable information to physicians during treatment and diagnosis of diseases. A number of approaches have been proposed to estimate tissue stiffness from the shear wave velocity. Optical coherence elastography offers a particularly high spatial and temporal resolution. However, current approaches typically acquire data at different positions sequentially, making it slow and less practical for clinical application. METHODS: We propose a new approach for elastography estimations using a fast imaging device to acquire small image volumes at rates of 831 Hz. The resulting sequence of phase image volumes is fed into a 4D convolutional neural network which handles both spatial and temporal data processing. We evaluate the approach on a set of image data acquired for gelatin phantoms of known elasticity. RESULTS: Using the neural network, the gelatin concentration of unseen samples was predicted with a mean error of 0.65 ± 0.81 percentage points from 90 subsequent volumes of phase data only. We achieve a data acquisition and data processing time of under 12 ms and 22 ms, respectively. CONCLUSIONS: We demonstrate direct volumetric optical coherence elastography from phase image data. The approach does not rely on particular stimulation or sampling sequences and allows the estimation of elastic tissue properties of up to 40 Hz. |
format | Online Article Text |
id | pubmed-7822782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-78227822021-02-11 4D deep learning for real-time volumetric optical coherence elastography Neidhardt, M. Bengs, M. Latus, S. Schlüter, M. Saathoff, T. Schlaefer, A. Int J Comput Assist Radiol Surg Short Communication PURPOSE: Elasticity of soft tissue provides valuable information to physicians during treatment and diagnosis of diseases. A number of approaches have been proposed to estimate tissue stiffness from the shear wave velocity. Optical coherence elastography offers a particularly high spatial and temporal resolution. However, current approaches typically acquire data at different positions sequentially, making it slow and less practical for clinical application. METHODS: We propose a new approach for elastography estimations using a fast imaging device to acquire small image volumes at rates of 831 Hz. The resulting sequence of phase image volumes is fed into a 4D convolutional neural network which handles both spatial and temporal data processing. We evaluate the approach on a set of image data acquired for gelatin phantoms of known elasticity. RESULTS: Using the neural network, the gelatin concentration of unseen samples was predicted with a mean error of 0.65 ± 0.81 percentage points from 90 subsequent volumes of phase data only. We achieve a data acquisition and data processing time of under 12 ms and 22 ms, respectively. CONCLUSIONS: We demonstrate direct volumetric optical coherence elastography from phase image data. The approach does not rely on particular stimulation or sampling sequences and allows the estimation of elastic tissue properties of up to 40 Hz. Springer International Publishing 2020-09-30 2021 /pmc/articles/PMC7822782/ /pubmed/32997312 http://dx.doi.org/10.1007/s11548-020-02261-5 Text en © The Author(s) 2020 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/. |
spellingShingle | Short Communication Neidhardt, M. Bengs, M. Latus, S. Schlüter, M. Saathoff, T. Schlaefer, A. 4D deep learning for real-time volumetric optical coherence elastography |
title | 4D deep learning for real-time volumetric optical coherence elastography |
title_full | 4D deep learning for real-time volumetric optical coherence elastography |
title_fullStr | 4D deep learning for real-time volumetric optical coherence elastography |
title_full_unstemmed | 4D deep learning for real-time volumetric optical coherence elastography |
title_short | 4D deep learning for real-time volumetric optical coherence elastography |
title_sort | 4d deep learning for real-time volumetric optical coherence elastography |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822782/ https://www.ncbi.nlm.nih.gov/pubmed/32997312 http://dx.doi.org/10.1007/s11548-020-02261-5 |
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