April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Low Cost Retinal Imaging for Diabetic Retinopathy Screening
Author Affiliations & Notes
  • M. S. Muller
    School of Optometry, Indiana University, Bloomington, Indiana
  • A. E. Elsner
    School of Optometry, Indiana University, Bloomington, Indiana
  • D. A. VanNasdale
    School of Optometry, Indiana University, Bloomington, Indiana
  • B. P. Haggerty
    School of Optometry, Indiana University, Bloomington, Indiana
  • T. D. Peabody
    School of Optometry, Indiana University, Bloomington, Indiana
  • R. C. Gustus
    School of Optometry, Indiana University, Bloomington, Indiana
  • B. L. Petrig
    School of Optometry, Indiana University, Bloomington, Indiana
  • Footnotes
    Commercial Relationships  M.S. Muller, Aeon Imaging LLC, E; IURTC, P; A.E. Elsner, Aeon Imaging LLC, I; IURTC, P; D.A. VanNasdale, None; B.P. Haggerty, None; T.D. Peabody, None; R.C. Gustus, None; B.L. Petrig, Aeon Imaging LLC, E; IURTC, P.
  • Footnotes
    Support  NIH Grants EB002346 (to AEE) and EY018772 (to BLP)
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 3305. doi:
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    • Get Citation

      M. S. Muller, A. E. Elsner, D. A. VanNasdale, B. P. Haggerty, T. D. Peabody, R. C. Gustus, B. L. Petrig; Low Cost Retinal Imaging for Diabetic Retinopathy Screening. Invest. Ophthalmol. Vis. Sci. 2009;50(13):3305.

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

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Abstract

Purpose: : To provide low-cost, nonmydriatic screening for diabetic retinopathy (DR) with our novel retinal imaging system, the laser scanning digital camera (LSDC). To provide a level of contrast of retinal vessels that is sufficient to monitor pathological changes and to provide a high sensitivity of referral.

Methods: : Our LSDC prototype is a confocal slit-scanning ophthalmoscope that uses a small pupil entrance / exit diameter of 2.5 mm to perform nonmydriatic, near infrared retinal imaging at 5.6 frames per second. A wide 36° imaging field of view and a working distance of 28 mm has been achieved. A single focusing knob permits easy adjustment over a wide range of visual acuity (+6 to -8 diopters). Pupil alignment is assisted in real-time with a second anterior segment camera, which also allows determination of pupil size and iris pigmentation in post-processing.An initial feasibility study of 61 participants aged 24 to 79 has been performed. This group includes 18 patients with mild to moderate DR and age-, gender- and race-matched controls. LSDC image quality was assessed by calculating the Michelson contrast over a major retinal artery or vein 2.5 optic disc diameters from the center of the optic nerve head. For each participant, a series of twenty images were acquired at different confocal aperture sizes for both fovea- and optic nerve head-centered views. The mean and standard deviation of the Michelson contrast were calculated from up to ten images per patient for the optic nerve head-centered datasets.

Results: : Images with a Michelson contrast of retinal vessels >0.15 are typical in our sample. There is no systematic loss of image quality observed between diabetic patients, their respective matched control subjects, or participants with darkly pigmented eyes. A repeatability study in 5 normal subjects, tested weekly over 4 weeks, resulted in an average coefficient of variation of <10% at each aperture size.

Conclusions: : Initial feasibility results have shown excellent potential for the LSDC to be used as a low-cost screening device for diabetic retinopathy.

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