Model-Based X-Ray-Induced Acoustic Computed Tomography.


Journal

IEEE transactions on ultrasonics, ferroelectrics, and frequency control
ISSN: 1525-8955
Titre abrégé: IEEE Trans Ultrason Ferroelectr Freq Control
Pays: United States
ID NLM: 9882735

Informations de publication

Date de publication:
12 2021
Historique:
pubmed: 27 7 2021
medline: 15 12 2021
entrez: 26 7 2021
Statut: ppublish

Résumé

X-ray-induced acoustic computed tomography (XACT) provides X-ray absorption-based contrast with acoustic detection. For its clinical translation, XACT imaging often has a limited field of view. This can result in image artifacts and overall loss of quantification accuracy. In this article, we aim to demonstrate model-based XACT image reconstruction to address these problems. An efficient matrix-free implementation of the regularized LSQR (MF-LSQR)-based minimization scheme and a noniterative model back-projection (MBP) scheme for computing XACT reconstructions have been demonstrated in this article. The proposed algorithms have been numerically validated and then used to perform reconstructions from experimental measurements obtained from an XACT setup. While the commonly used back-projection (BP) algorithm produces limited-view and noisy artifacts in the region of interest (ROI), model-based LSQR minimization overcomes these issues. The model-based algorithms also reduce the ring artifacts caused due to the nonuniformity response of the multichannel data acquisition. Using the model-based reconstruction algorithms, we are able to obtain reasonable XACT reconstructions for acoustic measurements of up to 120° view. Although the MBP is more efficient than the model-based LSQR algorithm, it provides only the structural information of the ROI. Overall, it has been demonstrated that the model-based image reconstruction yields better image quality for XACT than the standard BP. Moreover, the combination of model-based image reconstruction with different regularization methods can solve the limited-view problem for XACT imaging (in many realistic cases where the full-view dataset is unavailable), and hence pave the way for future clinical translation.

Identifiants

pubmed: 34310297
doi: 10.1109/TUFFC.2021.3098501
pmc: PMC8739265
mid: NIHMS1759212
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

3560-3569

Subventions

Organisme : NCI NIH HHS
ID : P30 CA062203
Pays : United States
Organisme : NCI NIH HHS
ID : R37 CA240806
Pays : United States

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