AI Article Synopsis

  • Recent research focuses on improving the localization of targets like vessels and tumors in photoacoustic (PA) images, which requires high signal-to-noise ratios (SNR).
  • To solve issues caused by optical scattering in deep tissues, a new deep learning method with a shared encoder and two decoders is proposed to enhance noise robustness and accurately extract target coordinates.
  • The effectiveness of this method is validated through training on simulated datasets and outperforming existing approaches in both simulated and clinical experimental PA data.

Article Abstract

A significant research problem of recent interest is the localization of targets like vessels, surgical needles, and tumors in photoacoustic (PA) images.To achieve accurate localization, a high photoacoustic signal-to-noise ratio (SNR) is required. However, this is not guaranteed for deep targets, as optical scattering causes an exponential decay in optical fluence with respect to tissue depth. To address this, we develop a novel deep learning method designed to explicitly exhibit robustness to noise present in photoacoustic radio-frequency (RF) data. More precisely, we describe and evaluate a deep neural network architecture consisting of a shared encoder and two parallel decoders. One decoder extracts the target coordinates from the input RF data while the other boosts the SNR and estimates clean RF data. The joint optimization of the shared encoder and dual decoders lends significant noise robustness to the features extracted by the encoder, which in turn enables the network to contain detailed information about deep targets that may be obscured by noise. Additional custom layers and newly proposed regularizers in the training loss function (designed based on observed RF data signal and noise behavior) serve to increase the SNR in the cleaned RF output and improve model performance. To account for depth-dependent strong optical scattering, our network was trained with simulated photoacoustic datasets of targets embedded at different depths inside tissue media of different scattering levels. The network trained on this novel dataset accurately locates targets in experimental PA data that is clinically relevant with respect to the localization of vessels, needles, or brachytherapy seeds. We verify the merits of the proposed architecture by outperforming the state of the art on both simulated and experimental datasets.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526152PMC
http://dx.doi.org/10.1109/TMI.2021.3077187DOI Listing

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