Evidence map›Paper›PMID 38923538›Full record

ArticleMedical physics2024

Estimation of threshold thickness of residual normal tissue in lung dysfunction detectable by dynamic chest radiography: A virtual imaging trial.

Shunya Yamaguchi, Rie Tanaka, Isao Matsumoto, Noriyuki Ohkura, William Paul Segars, Ehsan Abadi, Ehsan Samei

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Article in Medical physics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Shunya YamaguchiGraduate School of Health Sciences, Kanazawa University, Kanazawa, Ishikawa, Japan.
Rie TanakaCollege of Medical, Pharmaceutical & Health Sciences, Kanazawa University, Kanazawa, Ishikawa, Japan.
Isao MatsumotoDepartment of Thoracic Surgery, Kanazawa University, Kanazawa, Ishikawa, Japan.
Noriyuki OhkuraDepartment of Respiratory Medicine, Kanazawa University Hospital, Kanazawa, Ishikawa, Japan.
William Paul SegarsCarl E Ravin Advanced Imaging Labs, Department of Radiology, Duke University, Durham, North Carolina, USA.
Ehsan AbadiCarl E Ravin Advanced Imaging Labs, Department of Radiology, Duke University, Durham, North Carolina, USA.
Ehsan SameiCarl E Ravin Advanced Imaging Labs, Department of Radiology, Duke University, Durham, North Carolina, USA.

Funding

TR&D Project 3: Virtual ReadersP41EB028744 · NIBIB · DUKE UNIVERSITY · PI Ehsan Samei · 2021 to 2026
$7.8M
JSPS KAKENHI Fostering Joint International Research 21KK0286JSPS KAKENHI Grant-in-aid for Scientific Research 21H02866NIBIB NIH HHS P41 EB028744Tateishi Science and Technology Foundationthe National Institute of Health 5P41EB028744
6 · The paper itself

Abstract

backgroundDynamic chest radiography (DCR) is a recently developed functional x-ray imaging technique that detects pulmonary ventilation impairment as a decrease in changes in lung density during respiration. However, the diagnostic performance of DCR is uncertain owing to an insufficient number of clinical cases. One solution is virtual imaging trials (VITs), which is an emerging alternative method for efficiently evaluating medical imaging technology via computer simulation techniques. PURPOSE: This study aimed to estimate the typical threshold thickness of residual normal tissue below which the presence of emphysema may be detected by DCR via VITs using virtual patients with different physiques and a user-defined ground truth.

methodsTwenty extended cardiac-torso (XCAT) phantoms that exhibited changes in lung density during respiration were generated to simulate virtual patients. To simulate a locally collapsed lung, an air sphere was inserted into each lung regions in the phantom. The XCAT phantom was virtually projected using an x-ray simulator. The respiratory changes in pixel value (ΔPV) were measured on the projected air spheres (simulated lesions) to calculate the percentage of decrease (ΔPV%) relative to ΔPV

resultsFor each lung region in all body sizes, the ΔPV% decreased as the amount of residual normal tissue decreased and could be defined as a function of the amount of residual normal tissue in front of and behind the simulated lesions with high R

conclusionsThe performance of DCR-based pulmonary impairment assessment depends on the amount of residual normal tissue in front of and behind the lesion rather than on the lesion size. The performance curve can be defined as a function of the amount of residual normal tissue in each lung region with a specific threshold of normal tissue remaining where lesions become detectable, shown as a decrease in ΔPV. The results of VITs are expected to accelerate future clinical trials for DCR-based pulmonary function assessment.

Indexed as

LungPhantoms, ImagingRadiography, ThoracicComputer SimulationHumansImage Processing, Computer-AssistedRespirationUser-Computer Interfacedynamic chest radiographypulmonary ventilationvirtual imaging trial

Identifiers

PMID38923538
PMCPMC11489022

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