July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
Evaluation of a screening algorithm for detection of diabetic retinopathy based on quantitation of retinal pathological elements
Author Affiliations & Notes
  • Stine Byberg
    Steno Diabetes Center Copenhagen, Gentofte, Denmark
  • Dorte Vistisen
    Steno Diabetes Center Copenhagen, Gentofte, Denmark
  • Marit Eika Jørgsensen
    Steno Diabetes Center Copenhagen, Gentofte, Denmark
  • Marianne Valerius
    Steno Diabetes Center Copenhagen, Gentofte, Denmark
    Dept. of Ophthalmology, University Hospital Glostrup, Glostrup, Denmark
  • Javad Nouri Hajari
    Steno Diabetes Center Copenhagen, Gentofte, Denmark
    Dept. of Ophthalmology, University Hospital Glostrup, Glostrup, Denmark
  • Henrik Lund-Andersen
    Steno Diabetes Center Copenhagen, Gentofte, Denmark
    Dept. of Ophthalmology, University Hospital Glostrup, Glostrup, Denmark
  • Footnotes
    Commercial Relationships   Stine Byberg, None; Dorte Vistisen, None; Marit Jørgsensen, None; Marianne Valerius, None; Javad Hajari, None; Henrik Lund-Andersen, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 4798. doi:
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      Stine Byberg, Dorte Vistisen, Marit Eika Jørgsensen, Marianne Valerius, Javad Nouri Hajari, Henrik Lund-Andersen; Evaluation of a screening algorithm for detection of diabetic retinopathy based on quantitation of retinal pathological elements. Invest. Ophthalmol. Vis. Sci. 2019;60(9):4798.

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

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Abstract

Purpose : Diabetic retinopathy (DR) screening is generally recommended once yearly. However, among diabetes patients with glycemic dysregulation, it is recommended to reduce the interval length. At Steno Diabetes Center Copenhagen (SDCC), a diabetes clinic in Denmark, screening intervals are based on quantitation of pathological findings in both the macula and peripheral retina, resulting in individualized screening intervals, not necessarily following the recommended guidelines. We followed 6000 patients between 1/1-2003 – 1/5-2017 at SDCC and assessed whether the individualized screening interval lengths were adequate for optimal patient outcomes.

Methods : All screening intervals with planned interval lengths ≥12 months were assessed for occurrence of adverse events, defined as;
1)DR progression requiring treatment, at the following screening date
2)DR-related hospital contact or photocoagulation treatment within the planned interval
According to guidelines, patients were considered dysregulated if they had HbA1c levels ≥53 mmol/mol and/or hypertension (>130/80 mmHg) before the beginning of an interval.

Results : The average interval length was longer than recommended; 19.9 (SD 7.6) months among well-regulated patients and 19.4 (SD 7.1) months among dysregulated patients. Out of 20,251 screening intervals, 17,534 (87%) followed the planned interval. Among screenings following the planned interval, only 0.5% (n=88) resulted in an adverse event. Dysregulated patient intervals (82% of all intervals) experienced a significantly higher proportion of adverse events compared with intervals of well-regulated patients (0.55% vs. 0.28%, p<0.05). Adverse events were more frequent among type 2 diabetes compared with type 1 diabetes (0.71% vs. 0.40%, p<0.05), if screened within the planned interval. 1.62% experienced an adverse event if screened beyond the planned interval.

Conclusions : The present study supports the validity of the SDCC algorithm, introducing individualized screening intervals for patients with no to moderate DR, even though this resulted in longer than recommended screening intervals for both well-regulated and dysregulated patients. Although intervals among dysregulated patients more frequently resulted in an adverse event, the proportion of adverse events was still less than 1%. Further analyses will assess the optimal screening interval for the individual patient

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

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