4.1 Article

A Multi-Center Diabetes Eye Screening Study in Community Settings: Study Design and Methodology

Journal

OPHTHALMIC EPIDEMIOLOGY
Volume 23, Issue 2, Pages 109-115

Publisher

TAYLOR & FRANCIS INC
DOI: 10.3109/09286586.2015.1099682

Keywords

study design; Diabetes; methodology; tele-ophthalmology; eye screening

Categories

Funding

  1. Centers for Disease Control and Prevention
  2. Johns Hopkins University [5U58DP002653]
  3. University of Alabama at Birmingham [5U58DP002651]
  4. University of Miami [5U58DP002652]
  5. Wills Eye Hospital [5U58DP002655]
  6. Johns Hopkins University: Alcon Research Institute award
  7. University of Alabama at Birmingham: EyeSight Foundation of Alabama
  8. Research to Prevent Blindness Inc.
  9. Buck Trust

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Purpose: Diabetes is the leading cause of new cases of blindness among adults aged 20-74 years within the United States. The Innovative Network for Sight Research group (INSIGHT) designed the Diabetic Eye Screening Study (DESS) to examine the feasibility and short-term effectiveness of non-mydriatic diabetic retinopathy (DR) screening for adults with diabetes in community-based settings. Methods: Study enrollment began in December 2011 at four sites: an internal medicine clinic at a county hospital in Birmingham, Alabama; a Federally-qualified community healthcare center in Miami-Dade County, Florida; a university-affiliated outpatient pharmacy in Philadelphia, Pennsylvania; and a medical home in Winston-Salem, North Carolina. People 18 years or older with previously diagnosed diabetes were offered free DR screening using non-mydriatic retinal photography that was preceded by a brief questionnaire addressing demographic information and previous eye care use. Visual acuity was also measured for each eye. Images were evaluated at a telemedicine reading center by trained evaluators using the National Health System DR grading classification. Participants and their physicians were sent screening report results and telephoned for a follow-up survey 3 months post-screening to determine whether participants had sought follow-up comprehensive eye care and their experiences with the screening process. Results: Target enrollment at each site was a minimum of 500 persons. Three of the four sites met this enrollment goal. Conclusion: The INSIGHT/DESS is intended to establish the feasibility and short-term effectiveness of DR screening using non-mydriatic retinal photography in persons with diabetes who seek services in community-based clinic and pharmacy settings.

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