March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Automated Foveola Localization in Three Dimensional (3D) Optical Coherence Tomography (OCT) Images with Various Macular Pathologies
Author Affiliations & Notes
  • Yu-Ying Liu
    College of Computing, Georgia Institute of Technology, Atlanta, Georgia
  • Hiroshi Ishikawa
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
    Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania
  • Mei Chen
    Intel Science and Technology Center on Embedded Computing, Carnegie Mellon University, Pittsburgh, Pennsylvania
  • Gadi Wollstein
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
  • Joel S. Schuman
    UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
    Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania
  • James M. Rehg
    College of Computing, Georgia Institute of Technology, Atlanta, Georgia
  • Footnotes
    Commercial Relationships  Yu-Ying Liu, None; Hiroshi Ishikawa, None; Mei Chen, None; Gadi Wollstein, None; Joel S. Schuman, Carl Zeiss Meditec (P); James M. Rehg, None
  • Footnotes
    Support  NIH R01-EY013178, P30-EY008098; Eye and Ear Foundation (Pittsburgh, PA); Research to Prevent Blindness; and Intel Labs, Intel Corporation (Santa Clara, CA)
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 4081. doi:
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    • Get Citation

      Yu-Ying Liu, Hiroshi Ishikawa, Mei Chen, Gadi Wollstein, Joel S. Schuman, James M. Rehg; Automated Foveola Localization in Three Dimensional (3D) Optical Coherence Tomography (OCT) Images with Various Macular Pathologies. Invest. Ophthalmol. Vis. Sci. 2012;53(14):4081.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To develop an automated method to determine the foveola location (x, y) in macular 3D spectral domain (SD-) OCT images in either healthy or pathological conditions, for facilitating further analysis around this important landmark.

Methods: : SD-OCT macular scans (Macular Cube 200x200 protocol, 6x6x2 mm; Cirrus HD-OCT; Carl Zeiss Meditec, Inc., Dublin, CA) were obtained from healthy subjects and subjects with various macular diseases (a total of 170 scans from 170 eyes/ 126 subjects; dataset for training [89 eyes from 67 subjects: 30 healthy eyes, 28 with epiretinal membrane (ERM), 37 with macular edema (ME), 16 with age-related macular degeneration (AMD), 17 with macular hole (MH)], and dataset for testing [81 eyes from 59 subjects: 35 healthy eyes, 19 ERM, 31 ME, 13 AMD, 15 MH]). Two ophthalmologists labeled the x and y location of the foveola for each scan independently by going through all x-z and y-z frames. One expert’s labeling was used as the ground truth while the difference between the two experts was used to assess the inter-expert variability. In feature construction, for each sampled location, multi-scale spatially-distributed texture features were computed within the centered context cube/window in the 3D-OCT as well as the OCT en-face image, respectively. Structural Support Vector Machine was trained to discriminatively weigh the features so that the score at each sampled position is inversely proportional to the localization distance. A coarse-to-fine sliding window approach was used to identify the position with the best score. The Euclidean distance between the computed location and the ground truth was used to assess the performance.

Results: : The automated method achieved a mean localization distance compared to the ground truth of 91±53 um (3.03±1.77 pixels) [86±44 um (2.87±1.45 pixels) for healthy and 94±59 um (3.14±1.96 pixels) for diseased eyes]. The inter-expert labeling difference was 54±42 um (1.82±1.39 pixels) [53±41 um (1.78±1.37 pixels) for healthy and 55±43 um (1.84±1.42 pixels) for diseased eyes]. The difference in mean results between the automated method and the inter-expert variability is only 38 um (1.25 pixels), though the difference is statistically significant.

Conclusions: : The proposed automated data-driven method localized the foveola position within 91 um (3.03 pixels) on average from the ground truth, which is well within the anatomical size of the foveola diameter (350um). This method may effectively identify the location of the foveola in healthy or pathological conditions in 3D-OCT scans to facilitate further analysis.

Keywords: image processing • imaging/image analysis: non-clinical • imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) 
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