Optimized Spatial-Spectral CT for Multi-Material Decomposition.


Journal

Proceedings of SPIE--the International Society for Optical Engineering
ISSN: 0277-786X
Titre abrégé: Proc SPIE Int Soc Opt Eng
Pays: United States
ID NLM: 101524122

Informations de publication

Date de publication:
Jun 2019
Historique:
entrez: 12 11 2020
pubmed: 1 6 2019
medline: 1 6 2019
Statut: ppublish

Résumé

Spectral CT is an emerging modality that uses a data acquisition scheme with varied spectral responses to provide enhanced material discrimination in addition to the structural information of conventional CT. Existing clinical and preclinical designs with this capability include kV-switching, split-filtration, and dual-layer detector systems to provide two spectral channels of projection data. In this work, we examine an alternate design based on a spatial-spectral filter. This source-side filter is made up a linear array of materials that divide the incident x-ray beam into spectrally varied beamlets. This design allows for any number of spectral channels; however, each individual channel is sparse in the projection domain. Model-based iterative reconstruction methods can accommodate such sparse spatial-spectral sampling patterns and allow for the incorporation of advanced regularization. With the goal of an optimized physical design, we characterize the effects of design parameters including filter tile order and filter tile width and their impact on material decomposition performance. We present results of numerical simulations that characterize the impact of each design parameter using a realistic CT geometry and noise model to demonstrate feasibility. Results for filter tile order show little change indicating that filter order is a low-priority design consideration. We observe improved performance for narrower filter widths; however, the performance drop-off is relatively flat indicating that wider filter widths are also feasible designs.

Identifiants

pubmed: 33177785
doi: 10.1117/12.2534333
pmc: PMC7654953
mid: NIHMS1640731
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NIBIB NIH HHS
ID : F31 EB023783
Pays : United States
Organisme : NIBIB NIH HHS
ID : R21 EB026849
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007057
Pays : United States

Références

Phys Med Biol. 2010 Nov 21;55(22):6575-99
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pubmed: 31105376
Med Phys. 2017 Oct;44(10):5120-5127
pubmed: 28444761
Med Phys. 2009 Apr;36(4):1359-69
pubmed: 19472643
Radiology. 2015 Sep;276(3):637-53
pubmed: 26302388

Auteurs

Matthew Tivnan (M)

Department of Biomedical Engineering, Johns Hopkins University, 720 Rutland Ave., Baltimore MD 21205.

Wenying Wang (W)

Department of Biomedical Engineering, Johns Hopkins University, 720 Rutland Ave., Baltimore MD 21205.

Steven Tilley (S)

Department of Biomedical Engineering, Johns Hopkins University, 720 Rutland Ave., Baltimore MD 21205.

Jeffrey H Siewerdsen (JH)

Department of Biomedical Engineering, Johns Hopkins University, 720 Rutland Ave., Baltimore MD 21205.

J Webster Stayman (JW)

Department of Biomedical Engineering, Johns Hopkins University, 720 Rutland Ave., Baltimore MD 21205.

Classifications MeSH