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Analyzing Relative Flow Speeds in Diabetic Retinopathy Using Variable Interscan Time Analysis OCT Angiography
Malvika Arya1, Marco Bonini Filho2, Carl B Rebhun1
1New England Eye Center, Tufts Medical Center, Boston, Massachusetts.
Ophthalmology. Retina
|June 26, 2020
Summary
The VISTA algorithm visualizes blood flow in diabetic retinopathy (DR), revealing that microvascular changes like microaneurysms and neovascularization correlate with slower flow speeds, aiding DR progression understanding.
Area of Science:
- Ophthalmology
- Medical Imaging
- Vascular Biology
Background:
- Diabetic retinopathy (DR) is a leading cause of vision loss.
- Understanding microvascular changes in DR is crucial for effective treatment.
- Current OCT angiography (OCTA) methods have limitations in assessing blood flow dynamics.
Purpose of the Study:
- To analyze relative blood flow speeds in the microvascular changes associated with diabetic retinopathy (DR) using the VISTA algorithm.
- To explore the potential of VISTA as an extension of OCTA for assessing DR.
- To correlate blood flow characteristics with DR severity and specific vascular abnormalities.
Main Methods:
- A cross-sectional study involving 13 patients with varying DR severity.
- OCT angiography images of the fovea were acquired using a swept-source OCT device.
- The Variable Interscan Time Analysis (VISTA) algorithm was applied to visualize relative blood flow speeds.
Main Results:
- Microaneurysms, IRMAs, and neovascularization were linked to slower blood flow.
- Different DR features exhibited distinct flow patterns: slow for microaneurysms, turbulent for IRMAs, and variable for neovascularization.
- Increased DR severity correlated with globally slower flow speeds, particularly around the foveal avascular zone.
Conclusions:
- The VISTA algorithm provides valuable insights into DR pathogenesis by visualizing blood flow.
- VISTA overcomes limitations of standard OCTA, offering a potential tool for improved DR assessment.
- These findings enhance understanding of the pathogenic microvascular changes in diabetic retinopathy.

