Evidence map›Paper›PMID 34902159›Full record

ArticleMedical physics2022

A GPU-accelerated framework for individualized estimation of organ doses in digital tomosynthesis.

Shobhit Sharma, Anuj Kapadia, Justin Brown, William Paul Segars, Wesley Bolch, Ehsan Samei

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Article in Medical physics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Shobhit SharmaCenter for Virtual Imaging Trials and Carl E. Ravin Advanced Imaging Laboratories, Department of Radiology, Duke University School of Medicine, Durham, North Carolina, USA.
Anuj KapadiaCenter for Virtual Imaging Trials and Carl E. Ravin Advanced Imaging Laboratories, Department of Radiology, Duke University School of Medicine, Durham, North Carolina, USA.
Justin BrownDivision of Medical Physics, Department of Radiology, College of Medicine, University of Florida, Gainesville, Florida, USA.
William Paul SegarsCenter for Virtual Imaging Trials and Carl E. Ravin Advanced Imaging Laboratories, Department of Radiology, Duke University School of Medicine, Durham, North Carolina, USA.
Wesley BolchDivision of Medical Physics, Department of Radiology, College of Medicine, University of Florida, Gainesville, Florida, USA.
Ehsan SameiCenter for Virtual Imaging Trials and Carl E. Ravin Advanced Imaging Laboratories, Department of Radiology, Duke University School of Medicine, Durham, North Carolina, USA.
Duke University · USUniversity of Florida · USAdvanced Imaging Research (United States) · US

Funding

TR&D Project 3: Virtual ReadersP41EB028744 · NIBIB · DUKE UNIVERSITY · PI Ehsan Samei · 2021 to 2026
$7.8M
Simulation Tools for Dynamic CTR01EB001838 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI SAMEI, EHSAN, SEGARS, WILLIAM P · 2005 to 2023
$6.9M
NIBIB NIH HHS P41 EB028744NIBIB NIH HHS R01 EB001838NIH HHS P41EB028744NIH HHS R01EB001838
6 · The paper itself

Abstract

purposeEstimation of organ doses in digital tomosynthesis (DT) is challenging due to the lack of existing tools that accurately and flexibly model protocol- and view-specific collimations and motion trajectories of the source and detector for a variety of exam protocols, and the computational inefficiencies of conducting MC simulations. The purpose of this study was to overcome these limitations by developing and benchmarking a GPU-accelerated MC simulation framework compatible with patient-specific computational phantoms for individualized estimation of organ doses in DT. MATERIALS AND

methodsThe framework for individualized estimation of dose in DT was developed as a two-step workflow: (1) a custom MATLAB code that accepts a patient-specific computational phantom and exam description (organ markers for defining the extremities of the anatomical region of interest, tube voltage, source-to-image distance, angular sweep range, number of projection views, and the pivot point to image distance - PPID) to compute the field of views (FOVs) for a clinical DT system, and (2) a MC tool (developed using MC-GPU) modeling the configuration of a clinical DT system to estimate organ doses based on the computed FOVs. Using this framework, we estimated organ doses for 28 radiosensitive organs in an adult reference patient model (M; 30 years) imaged using a commercial DT system (VolumeRad, GE Healthcare, Waukesha, WI). The estimates were benchmarked against values from a comparable organ dose estimation framework (reference dataset developed by the Advanced Laboratory for Radiation Dosimetry Studies at University of Florida) for a posterior-anterior chest exam. The resulting differences were quantified as percent relative errors and analyzed to identify any potential sources of bias and uncertainties. The timing performance (run duration in seconds) of the framework was also quantified for the same simulation to gauge the feasibility of the workflow for time-constrained clinical applications.

resultsThe organ dose estimates from the developed framework showed a close agreement with the reference dataset, with percent relative errors ranging from -6.9% to 5.0% and a mean absolute percent difference of 1.7% over all radiosensitive organs, with the exception of testes and eye lens, for which the percent relative errors were higher at -18.9% and -27.6%, respectively, due to their relative positioning outside the primary irradiation field, leading to fewer photons depositing energy and consequently higher errors in estimated organ doses. The run duration for the same simulation was 916.3 s, representing a substantial improvement in performance over existing nonparallelized MC tools.

conclusionsThis study successfully developed and benchmarked a GPU-accelerated framework compatible with patient-specific anthropomorphic computational phantoms for accurate individualized estimation of organ doses in DT. By enabling patient-specific estimation of organ doses, this framework can aid clinicians and researchers by providing them with tools essential for tracking the radiation burden to patients for dose monitoring purposes and identifying the trends and relationships in organ doses for a patient population to optimize existing and develop new exam protocols.

Indexed as

RadiometryTomography, X-Ray ComputedAdultHumansMonte Carlo MethodPhantoms, ImagingRadiation DosageMonte Carloradiation dosimetry and risktomosynthesis

Identifiers

PMID34902159
PMCPMC8828666
OpenAlexW4200386911

What OpenQuestion holds

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Registered trials

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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.