Evidence map›Paper›PMID 29622855›Full record

ArticleProceedings of SPIE--the International Society for Optical Engineering2018

Prospective Image Quality Analysis and Control for Prior-Image-Based Reconstruction of Low-Dose CT.

Hao Zhang, Grace J Gang, Hao Dang, Marc S Sussman, Cheng Ting Lin, Jeffrey H Siewerdsen, J Webster Stayman

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In one paragraph

Article in Proceedings of SPIE--the International Society for Optical Engineering, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hao ZhangDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21205, USA.
Grace J GangDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21205, USA.
Hao DangDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21205, USA.
Marc S SussmanDepartment of Surgery, Johns Hopkins University, Baltimore, MD 21205, USA.
Cheng Ting LinDepartment of Radiology and Radiologic Science, Johns Hopkins University, Baltimore, MD 21205, USA.
Jeffrey H SiewerdsenDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21205, USA.
J Webster StaymanDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21205, USA.

Funding

Prior-image-based CT reconstruction for low-dose lung cancer screeningR21CA219608 · NCI · JOHNS HOPKINS UNIVERSITY · PI STAYMAN, JOSEPH WEBSTER · 2017 to 2018
$391k
NCI NIH HHS R21 CA219608
6 · The paper itself

Abstract

purposePrior-image-based reconstruction (PIBR) is a powerful tool for low-dose CT, however, the nonlinear behavior of such approaches are generally difficult to predict and control. Similarly, traditional image quality metrics do not capture potential biases exhibited in PIBR images. In this work, we identify a new bias metric and construct an analytical framework for prospectively predicting and controlling the relationship between prior image regularization strength and this bias in a reliable and quantitative fashion.

methodsBias associated with prior image regularization in PIBR can be described as the fraction of actual contrast change (between the prior image and current anatomy) that appears in the reconstruction. Using local approximation of the nonlinear PIBR objective, we develop an analytical relationship between local regularization, fractional contrast reconstructed, and true contrast change. This analytic tool allows prediction bias properties in a reconstructed PIBR image and includes the dependencies on the data acquisition, patient anatomy and change, and reconstruction parameters. Predictions are leveraged to provide reliable and repeatable image properties for varying data fidelity in simulation and physical cadaver experiments.

resultsThe proposed analytical approach permits accurate prediction of reconstructed contrast relative to a gold standard based on exhaustive search based on numerous iterative reconstructions. The framework is used to control regularization parameters to enforce consistent change reconstructions over varying fluence levels and varying numbers of projection angles - enabling bias properties that are less location- and acquisition-dependent.

conclusionsWhile PIBR methods have demonstrated a substantial ability for dose reduction, image properties associated with those images have been difficult to express and quantify using traditional metrics. The novel framework presented in this work not only quantifies this bias in an intuitive fashion, but it gives a way to predict and control the bias. Reliable and predictable reconstruction methods are a requirement for clinical imaging systems and the proposed framework is an important step translating PIBR methods to clinical application.

Identifiers

PMID29622855
PMCPMC5881925

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.