Samenvatting
Shear-wave elastography (SWE) permits local estimation of tissue elasticity, an important imaging marker in biomedicine. This recently developed, advanced technique assesses the speed of a laterally traveling shear wave after an acoustic radiation force "push" to estimate local Young's moduli in an operator-independent fashion. In this work, we show how synthetic SWE (sSWE) images can be generated based on conventional B-mode imaging through deep learning. Using side-by-side-view B-mode/SWE images collected in 50 patients with prostate cancer, we show that sSWE images with a pixel-wise mean absolute error of 4.5 ± 0.96 kPa with regard to the original SWE can be generated. Visualization of high-level feature levels through t -distributed stochastic neighbor embedding reveals substantial overlap between data from two different scanners. Qualitatively, we examined the use of the sSWE methodology for B-mode images obtained with a scanner without SWE functionality. We also examined the use of this type of network in elasticity imaging in the thyroid. Limitations of the technique reside in the fact that networks have to be retrained for different organs, and that the method requires standardization of the imaging settings and procedure. Future research will be aimed at the development of sSWE as an elasticity-related tissue typing strategy that is solely based on B-mode ultrasound acquisition, and the examination of its clinical utility.
Originele taal-2 | Engels |
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Artikelnummer | 9046008 |
Pagina's (van-tot) | 2640-2648 |
Aantal pagina's | 9 |
Tijdschrift | IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control |
Volume | 67 |
Nummer van het tijdschrift | 12 |
Vroegere onlinedatum | 24 mrt. 2020 |
DOI's | |
Status | Gepubliceerd - dec. 2020 |
Financiering
Manuscript received January 11, 2020; accepted March 18, 2020. Date of publication March 24, 2020; date of current version November 23, 2020. This work was supported in part by the Dutch Cancer Society under Grant UVA2013-5941, in part by the European Research Council Starting Grant under Grant 280209, and in part by the framework of the IMPULS2-Program within the Eindhoven University of Technology in collaboration with Philips. (Corresponding author: R. R. Wildeboer.) R. R. Wildeboer, R. J. G. van Sloun, and M. Mischi are with the Laboratory of Biomedical Diagnostics, Department of Electrical Engineering, Eindhoven University of Technology, 5612 AZ Eindhoven, The Netherlands (e-mail: [email protected]; [email protected]).
Financiers | Financiernummer |
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Dutch Cancer Society | UVA2013-5941 |
European Union’s Horizon Europe research and innovation programme | 875067 |
Seventh Framework Programme | 280209 |
European Research Council | |
Technische Universiteit Eindhoven |