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Photon-counting computed tomography versus energy-integrating computed tomography for detection of small liver lesions: comparison using a virtual framework imaging.

Publication ,  Journal Article
Felice, N; Wildman-Tobriner, B; Segars, WP; Bashir, MR; Marin, D; Samei, E; Abadi, E
Published in: J Med Imaging (Bellingham)
September 2024

PURPOSE: Photon-counting computed tomography (PCCT) has the potential to provide superior image quality to energy-integrating CT (EICT). We objectively compare PCCT to EICT for liver lesion detection. APPROACH: Fifty anthropomorphic, computational phantoms with inserted liver lesions were generated. Contrast-enhanced scans of each phantom were simulated at the portal venous phase. The acquisitions were done using DukeSim, a validated CT simulation platform. Scans were simulated at two dose levels ( CTDI vol 1.5 to 6.0 mGy) modeling PCCT (NAEOTOM Alpha, Siemens, Erlangen, Germany) and EICT (SOMATOM Flash, Siemens). Images were reconstructed with varying levels of kernel sharpness (soft, medium, sharp). To provide a quantitative estimate of image quality, the modulation transfer function (MTF), frequency at 50% of the MTF ( f 50 ), noise magnitude, contrast-to-noise ratio (CNR, per lesion), and detectability index ( d ' , per lesion) were measured. RESULTS: Across all studied conditions, the best detection performance, measured by d ' , was for PCCT images with the highest dose level and softest kernel. With soft kernel reconstruction, PCCT demonstrated improved lesion CNR and d ' compared with EICT, with a mean increase in CNR of 35.0% ( p < 0.001 ) and 21% ( p < 0.001 ) and a mean increase in d ' of 41.0% ( p < 0.001 ) and 23.3% ( p = 0.007 ) for the 1.5 and 6.0 mGy acquisitions, respectively. The improvements were greatest for larger phantoms, low-contrast lesions, and low-dose scans. CONCLUSIONS: PCCT demonstrated objective improvement in liver lesion detection and image quality metrics compared with EICT. These advances may lead to earlier and more accurate liver lesion detection, thus improving patient care.

Duke Scholars

Published In

J Med Imaging (Bellingham)

DOI

ISSN

2329-4302

Publication Date

September 2024

Volume

11

Issue

5

Start / End Page

053502

Location

United States

Related Subject Headings

  • 4003 Biomedical engineering
  • 3202 Clinical sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Felice, N., Wildman-Tobriner, B., Segars, W. P., Bashir, M. R., Marin, D., Samei, E., & Abadi, E. (2024). Photon-counting computed tomography versus energy-integrating computed tomography for detection of small liver lesions: comparison using a virtual framework imaging. J Med Imaging (Bellingham), 11(5), 053502. https://doi.org/10.1117/1.JMI.11.5.053502
Felice, Nicholas, Benjamin Wildman-Tobriner, William Paul Segars, Mustafa R. Bashir, Daniele Marin, Ehsan Samei, and Ehsan Abadi. “Photon-counting computed tomography versus energy-integrating computed tomography for detection of small liver lesions: comparison using a virtual framework imaging.J Med Imaging (Bellingham) 11, no. 5 (September 2024): 053502. https://doi.org/10.1117/1.JMI.11.5.053502.
Felice N, Wildman-Tobriner B, Segars WP, Bashir MR, Marin D, Samei E, et al. Photon-counting computed tomography versus energy-integrating computed tomography for detection of small liver lesions: comparison using a virtual framework imaging. J Med Imaging (Bellingham). 2024 Sep;11(5):053502.
Felice, Nicholas, et al. “Photon-counting computed tomography versus energy-integrating computed tomography for detection of small liver lesions: comparison using a virtual framework imaging.J Med Imaging (Bellingham), vol. 11, no. 5, Sept. 2024, p. 053502. Pubmed, doi:10.1117/1.JMI.11.5.053502.
Felice N, Wildman-Tobriner B, Segars WP, Bashir MR, Marin D, Samei E, Abadi E. Photon-counting computed tomography versus energy-integrating computed tomography for detection of small liver lesions: comparison using a virtual framework imaging. J Med Imaging (Bellingham). 2024 Sep;11(5):053502.

Published In

J Med Imaging (Bellingham)

DOI

ISSN

2329-4302

Publication Date

September 2024

Volume

11

Issue

5

Start / End Page

053502

Location

United States

Related Subject Headings

  • 4003 Biomedical engineering
  • 3202 Clinical sciences