Advertisement

Evaluation of a System for Automatic Detection of Diabetic Retinopathy From Color Fundus Photographs in a Large Population of Patients With Diabetes

  1. Michael D. Abràmoff, MD, PHD123,
  2. Meindert Niemeijer, PHD34,
  3. Maria S.A. Suttorp-Schulten, MD, PHD5,
  4. Max A. Viergever, PHD4,
  5. Stephen R. Russell, MD12 and
  6. Bram van Ginneken, PHD4
  1. 1Retina Service, Department of Ophthalmology and Visual Sciences, University of Iowa Hospitals and Clinics, Iowa City, Iowa
  2. 2Department of Veterans Affairs, Iowa City VA Medical Center, Iowa City, Iowa
  3. 3Department of Electrical and Computer Engineering, University of Iowa, Iowa City, Iowa
  4. 4Image Sciences Institute, University Medical Center Utrecht, Utrecht, the Netherlands
  5. 5Ophthalmology Service, OLVG Hospital, Amsterdam, the Netherlands
  1. Address correspondence and reprint requests to Michael D. Abràmoff, University of Iowa, Ophthalmology & Visual Sciences, 200 Hawkins Dr., Room 11180Q, Iowa City, Iowa 52242. E-mail: michael-abramoff{at}uiowa.edu

Abstract

OBJECTIVE—To evaluate the performance of a system for automated detection of diabetic retinopathy in digital retinal photographs, built from published algorithms, in a large, representative, screening population.

RESEARCH DESIGN AND METHODS—We conducted a retrospective analysis of 10,000 consecutive patient visits, specifically exams (four retinal photographs, two left and two right) from 5,692 unique patients from the EyeCheck diabetic retinopathy screening project imaged with three types of cameras at 10 centers. Inclusion criteria included no previous diagnosis of diabetic retinopathy, no previous visit to ophthalmologist for dilated eye exam, and both eyes photographed. One of three retinal specialists evaluated each exam as unacceptable quality, no referable retinopathy, or referable retinopathy. We then selected exams with sufficient image quality and determined presence or absence of referable retinopathy. Outcome measures included area under the receiver operating characteristic curve (number needed to miss one case [NNM]) and type of false negative.

RESULTS—Total area under the receiver operating characteristic curve was 0.84, and NNM was 80 at a sensitivity of 0.84 and a specificity of 0.64. At this point, 7,689 of 10,000 exams had sufficient image quality, 4,648 of 7,689 (60%) were true negatives, 59 of 7,689 (0.8%) were false negatives, 319 of 7,689 (4%) were true positives, and 2,581 of 7,689 (33%) were false positives. Twenty-seven percent of false negatives contained large hemorrhages and/or neovascularizations.

CONCLUSIONS—Automated detection of diabetic retinopathy using published algorithms cannot yet be recommended for clinical practice. However, performance is such that evaluation on validated, publicly available datasets should be pursued. If algorithms can be improved, such a system may in the future lead to improved prevention of blindness and vision loss in patients with diabetes.

Footnotes

  • Published ahead of print at http://care.diabetesjournals.org on 16 November 2007. DOI: 10.2337/dc07-1312.

    M.D.A. is a director and shareholder of iOptics.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C Section 1734 solely to indicate this fact.

    • Accepted November 8, 2007.
    • Received September 3, 2007.
| Table of Contents

This Article

  1. Diabetes Care February 2008 vol. 31 no. 2 193-198
  1. All Versions of this Article:
    1. dc07-1312v1
    2. 31/2/193 most recent
Advertisement