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Systematic analysis of bias and variability of morphologic features for lung lesions in computed tomography.

Publication ,  Journal Article
Hoye, J; Solomon, J; Sauer, TJ; Robins, M; Samei, E
Published in: J Med Imaging (Bellingham)
January 2019

We propose to characterize the bias and variability of quantitative morphology features of lung lesions across a range of computed tomography (CT) imaging conditions. A total of 15 lung lesions were simulated (five in each of three spiculation classes: low, medium, and high). For each lesion, a series of simulated CT images representing different imaging conditions were synthesized by applying three-dimensional blur and adding correlated noise based on the measured noise and resolution properties of five commercial multislice CT systems, representing three dose levels ( CTDI vol of 1.90, 3.75, 7.50 mGy), three slice thicknesses (0.625, 1.25, 2.5 mm), and 33 clinical reconstruction kernels from five clinical scanners. The images were segmented using three segmentation algorithms and each algorithm was evaluated by computing a Sørensen-Dice coefficient between the ground truth and the segmentation. A series of 21 shape-based morphology features were extracted from both "ground truth" (i.e., preblur without noise) and "image rendered" lesions (i.e., postblur and with noise). For each morphology feature, the bias was quantified by comparing the percentage relative error in the morphology metric between the imaged lesions and the ground-truth lesions. The variability was characterized by calculating the average coefficient of variation averaged across repeats and imaging conditions. The active contour segmentation had the highest average Dice coefficient of 0.80 followed by 0.63 for threshold, and 0.39 for fuzzy c-means. The bias of the features was segmentation algorithm and feature-dependent, with sharper kernels being less biased and smoother kernels being more biased in general. The feature variability from simulated images ranged from 0.30% to 10% for repeats of the same condition and from 0.74% to 25.3% for different lesions in the same spiculation class. In conclusion, the bias of morphology features is dependent on the acquisition protocol in combination with the segmentation algorithm used and the variability is primarily dependent on the segmentation algorithm.

Duke Scholars

Published In

J Med Imaging (Bellingham)

DOI

ISSN

2329-4302

Publication Date

January 2019

Volume

6

Issue

1

Start / End Page

013504

Location

United States

Related Subject Headings

  • 4003 Biomedical engineering
  • 3202 Clinical sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Hoye, J., Solomon, J., Sauer, T. J., Robins, M., & Samei, E. (2019). Systematic analysis of bias and variability of morphologic features for lung lesions in computed tomography. J Med Imaging (Bellingham), 6(1), 013504. https://doi.org/10.1117/1.JMI.6.1.013504
Hoye, Jocelyn, Justin Solomon, Thomas J. Sauer, Marthony Robins, and Ehsan Samei. “Systematic analysis of bias and variability of morphologic features for lung lesions in computed tomography.J Med Imaging (Bellingham) 6, no. 1 (January 2019): 013504. https://doi.org/10.1117/1.JMI.6.1.013504.
Hoye J, Solomon J, Sauer TJ, Robins M, Samei E. Systematic analysis of bias and variability of morphologic features for lung lesions in computed tomography. J Med Imaging (Bellingham). 2019 Jan;6(1):013504.
Hoye, Jocelyn, et al. “Systematic analysis of bias and variability of morphologic features for lung lesions in computed tomography.J Med Imaging (Bellingham), vol. 6, no. 1, Jan. 2019, p. 013504. Pubmed, doi:10.1117/1.JMI.6.1.013504.
Hoye J, Solomon J, Sauer TJ, Robins M, Samei E. Systematic analysis of bias and variability of morphologic features for lung lesions in computed tomography. J Med Imaging (Bellingham). 2019 Jan;6(1):013504.

Published In

J Med Imaging (Bellingham)

DOI

ISSN

2329-4302

Publication Date

January 2019

Volume

6

Issue

1

Start / End Page

013504

Location

United States

Related Subject Headings

  • 4003 Biomedical engineering
  • 3202 Clinical sciences