DukeSim: A Realistic, Rapid, and Scanner-Specific Simulation Framework in Computed Tomography.


Journal Article

The purpose of this study was to develop a CT simulation platform that is: 1) compatible with voxel-based computational phantoms; 2) capable of modeling the geometry and physics of commercial CT scanners; and 3) computationally efficient. Such a simulation platform is designed to enable the virtual evaluation and optimization of CT protocols and parameters for achieving a targeted image quality while reducing radiation dose. Given a voxelized computational phantom and a parameter file describing the desired scanner and protocol, the developed platform DukeSim calculates projection images using a combination of ray-tracing and Monte Carlo techniques. DukeSim includes detailed models for the detector quantum efficiency, quantum and electronic noise, detector crosstalk, subsampling of the detector and focal spot areas, focal spot wobbling, and the bowtie filter. DukeSim was accelerated using GPU computing. The platform was validated using physical and computational versions of a phantom (Mercury phantom). Clinical and simulated CT scans of the phantom were acquired at multiple dose levels using a commercial CT scanner (Somatom Definition Flash; Siemens Healthcare). The real and simulated images were compared in terms of image contrast, noise magnitude, noise texture, and spatial resolution. The relative error between the clinical and simulated images was less than 1.4%, 0.5%, 2.6%, and 3%, for image contrast, noise magnitude, noise texture, and spatial resolution, respectively, demonstrating the high realism of DukeSim. The runtime, dependent on the imaging task and the hardware, was approximately 2-3 minutes per rotation in our study using a computer with 4 GPUs. DukeSim, when combined with realistic human phantoms, provides the necessary toolset with which to perform large-scale and realistic virtual clinical trials in a patient and scanner-specific manner.

Full Text

Duke Authors

Cited Authors

  • Abadi, E; Harrawood, B; Sharma, S; Kapadia, A; Segars, WP; Samei, E

Published Date

  • June 2019

Published In

Volume / Issue

  • 38 / 6

Start / End Page

  • 1457 - 1465

PubMed ID

  • 30561344

Pubmed Central ID

  • 30561344

Electronic International Standard Serial Number (EISSN)

  • 1558-254X

Digital Object Identifier (DOI)

  • 10.1109/TMI.2018.2886530


  • eng

Conference Location

  • United States