July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
Development of AI Deep Learning Algorithms for the Quantification of Retinopathy of Prematurity
Author Affiliations & Notes
  • Phanith Touch
    School of Medicine, University of Washington, Seattle, Washington, United States
  • Yue Wu
    Department of Ophthalmology, University of Washington, Seattle, Washington, United States
  • Yuka Kihara
    Department of Ophthalmology, University of Washington, Seattle, Washington, United States
  • Emily Marie Zepeda
    Department of Ophthalmology, University of Washington, Seattle, Washington, United States
  • Thomas Bradford Gillette
    Department of Ophthalmology, Seattle Children's Hospital, Seattle, Washington, United States
  • Michelle Trager Cabrera
    Department of Ophthalmology, Seattle Children's Hospital, Seattle, Washington, United States
    Department of Ophthalmology, University of Washington, Seattle, Washington, United States
  • Aaron Lee
    Department of Ophthalmology, University of Washington, Seattle, Washington, United States
    Department of Ophthalmology, Puget Sound Veteran Affairs, Seattle, Washington, United States
  • Footnotes
    Commercial Relationships   Phanith Touch, None; Yue Wu, None; Yuka Kihara, None; Emily Zepeda, None; Thomas Gillette, None; Michelle Cabrera, None; Aaron Lee, Carl-Zeiss Meditec Inc (F), Microsoft Corporation (F), Novartis Pharmaceuticals (F), NVIDIA Corporation (F), Topcon Corporation (R)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 1530. doi:
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    • Get Citation

      Phanith Touch, Yue Wu, Yuka Kihara, Emily Marie Zepeda, Thomas Bradford Gillette, Michelle Trager Cabrera, Aaron Lee; Development of AI Deep Learning Algorithms for the Quantification of Retinopathy of Prematurity. Invest. Ophthalmol. Vis. Sci. 2019;60(9):1530.

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

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Abstract

Purpose : Retinopathy of prematurity (ROP) remains a leading cause of childhood blindness worldwide. Recently, handheld spectral-domain optical coherence tomography (SD-OCT) has become more widely used in neonates because it allows for non-invasive, quick in vivo imaging of the retinal structures offering more detail than clinical examination. However, objective quantification of SD-OCT images are difficult because they require time-consuming human expert interpretation. We sought to create a fully automated algorithm to identify and quantify the ROP clinical features in SD-OCT images from neonates.

Methods : 4,687 SD-OCT images from 54 neonates were collected. A fully automated pipeline was created 1) to segment the border between the vitreous and internal limiting membrane and 2) detection of vitreous punctate hyperreflective opacities (VHO) using deep learning and Gaussian convolutions, respectively. The data was partitioned by neonate into training, validation, and test sets. A total of 4 independent expert graders created the ground truth for each image in the test set, which were used to validate the models. We tested the performance of the automated pipeline using Dice coefficient and F1 score.

Results : The mean Dice coefficients for the human interrater reliability and the models for the vitreous border segmentation were 0.95 (SD=0.12) and 0.90 (SD=0.21), respectively (Wilcoxon p<0.05). The mean F1 scores for the human interrater reliability and the models for VHO detection were 0.75 (SD=0.25) and 0.68 (SD=0.33), respectively (Wilcoxon p=0.60).

Conclusions : Deep learning models can achieve high accuracy in identifying and detecting certain clinical features of ROP. Features with subjective manual quantification such as VHO may eventually be screened using fully automated algorithms. Further studies are needed to extend the pipeline to include other clinical features such as cystoid macular edema and vitreous bands.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

 

Figure 1. Deep learning model schematic. Modified U-Net architecture for vitreous and internal limiting membrane segmentation.

Figure 1. Deep learning model schematic. Modified U-Net architecture for vitreous and internal limiting membrane segmentation.

 

Figure 2. Example segmentations of the vitreous border (top) and punctate hyperreflective opacities (bottom). The left column shows the original image, the middle column shows expert segmentation, and the far right column shows segmentation by the models. Insets are zoomed images of opacities.

Figure 2. Example segmentations of the vitreous border (top) and punctate hyperreflective opacities (bottom). The left column shows the original image, the middle column shows expert segmentation, and the far right column shows segmentation by the models. Insets are zoomed images of opacities.

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