July 2018
Volume 59, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2018
Risk assessment in retinopathy of prematurity: improvement of clinical models using automated image analysis
Author Affiliations & Notes
  • Jayashree Kalpathy-Cramer
    Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, Massachusetts, United States
    Center for Clinical Data Science, Massachusetts General Hospital & Brigham and Women's Hospital, Boston, Massachusetts, United States
  • James M Brown
    Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, Massachusetts, United States
  • J. Peter Campbell
    Ophthalmology, Oregon Health & Science University, Boston, Massachusetts, United States
  • Susan Ostmo
    Ophthalmology, Oregon Health & Science University, Boston, Massachusetts, United States
  • Peng Tian
    Electrical and Computer Engineering, Northeastern University, Boston, Massachusetts, United States
  • Veysi Yildiz
    Electrical and Computer Engineering, Northeastern University, Boston, Massachusetts, United States
  • Sang Jin Kim
    Ophthalmology, Oregon Health & Science University, Boston, Massachusetts, United States
    Ophthalmology, Samsung Medical Center, Seoul, Korea (the Republic of)
  • Robison Vernon Paul Chan
    Ophthalmology, University of Illinois at Chicago, Chicago, Illinois, United States
  • Jennifer Dy
    Electrical and Computer Engineering, Northeastern University, Boston, Massachusetts, United States
  • Deniz Erdogmus
    Electrical and Computer Engineering, Northeastern University, Boston, Massachusetts, United States
  • Stratis Ioannidis
    Electrical and Computer Engineering, Northeastern University, Boston, Massachusetts, United States
  • Michael F Chiang
    Ophthalmology and Medical Informatics, Oregon Health & Science University, Portland, Oregon, United States
  • Footnotes
    Commercial Relationships   Jayashree Kalpathy-Cramer, INFOTECH Soft, Inc. (C); James Brown, None; J. Peter Campbell, None; Susan Ostmo, None; Peng Tian, None; Veysi Yildiz, None; Sang Kim, None; Robison Chan, Allergan (C), Bausch and Lomb (C), Visunex (C); Jennifer Dy, None; Deniz Erdogmus, None; Stratis Ioannidis, None; Michael Chiang, Clarity Medical Systems (S), National Eye Institute (F), Novartis (C)
  • Footnotes
    Support  Supported by NIH (R01EY019474, P30EY10572, P41EB015896), NSF (SCH-1622542 at MGH; SCH-1622536 at Northeastern; SCH-1622679 at OHSU), and by unrestricted departmental funding from Research to Prevent Blindness (OHSU).
Investigative Ophthalmology & Visual Science July 2018, Vol.59, 2767. doi:
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    • Get Citation

      Jayashree Kalpathy-Cramer, James M Brown, J. Peter Campbell, Susan Ostmo, Peng Tian, Veysi Yildiz, Sang Jin Kim, Robison Vernon Paul Chan, Jennifer Dy, Deniz Erdogmus, Stratis Ioannidis, Michael F Chiang; Risk assessment in retinopathy of prematurity: improvement of clinical models using automated image analysis. Invest. Ophthalmol. Vis. Sci. 2018;59(9):2767.

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

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Abstract

Purpose : ROP risk is traditionally predicted using clinical parameters such as birth weight, gestational age, and systemic illness. We propose that risk models for predicting treatment-requiring (Type 1) ROP may be improved with the inclusion of image severity scores derived from a deep learning algorithm.

Methods : A multi-institutional dataset of posterior retinal photographs was collected as part of the ongoing “Imaging and Informatics in ROP” (i-ROP) study. A reference standard diagnosis (RSD) for treatment-requiring ROP was assigned to each image using previously published methods. An i-ROP image severity score for plus disease (i-ROP-SS) was automatically computed using a deep convolutional neural network, which grades images on a scale from 1.0 - 9.0. The change in severity between first and second sessions (Δi-ROP-SS) was also calculated, per subject. Clinical parameters included birth weight, gestational age, target oxygen saturation, chronic lung disease, intraventricular hemorrhage grade, and sepsis. Five logistic regression models were constructed and compared to predict whether an infant would require treatment: (1) clinical parameters only, (2) clinical parameters, i-ROP-SS at baseline, (3) clinical parameters, i-ROP-SS at baseline, Δi-ROP-SS at follow-up, (4) i-ROP-SS at baseline, Δi-ROP-SS at follow-up, (5) birth weight, gestational age, i-ROP-SS at baseline, Δi-ROP-SS at follow-up. All models were evaluated using five-fold stratified cross-validation.

Results : Mean ± standard deviation areas under the receiver operating curve (AUCs) were (1) 0.85±0.05, (2) 0.89±0.06, (3) 0.93±0.05, (4) 0.84±0.15 and (5) 0.91±0.06. Both the mean sensitivity and specificity of risk model (3) were 89%. The high specificity is favorable compared with previous models such WINROP (95.7% specificity, 24% sensitivity), CO-ROP (96.4% sensitivity, 33.7% specificity), CHOP-ROP (98% sensitivity, 53% specificity).

Conclusions : Inclusion of a deep learning-based image severity score in risk models improves their power in predicting treatment-requiring ROP. This may have implications for clinical ROP management.

This is an abstract that was submitted for the 2018 ARVO Annual Meeting, held in Honolulu, Hawaii, April 29 - May 3, 2018.

 

Table summarizing data and AUCs in each of the logistic regression risk models.

Table summarizing data and AUCs in each of the logistic regression risk models.

 

Areas under the ROC curve (mean + standard deviation) for risk models (1) clinical only, and (3) clinical parameters, i-ROP-SS at baseline, Δi-ROP-SS at follow-up.

Areas under the ROC curve (mean + standard deviation) for risk models (1) clinical only, and (3) clinical parameters, i-ROP-SS at baseline, Δi-ROP-SS at follow-up.

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