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Updated: Sep 24, 2025

Quantitative Fundus Autofluorescence for the Evaluation of Retinal Diseases
Published on: March 11, 2016
OCTA changes following loading phase with intravitreal aflibercept for DME.
Vinay Kansal1, Kevin Colleaux2, Nigel Rawlings2
1Department of Ophthalmology, Saskatoon City Hospital and the University of Saskatchewan, Saskatoon, Sask.
Intravitreal aflibercept treatment for diabetic macular edema (DME) reduced superficial vascular plexus density in responders. However, pretreatment optical coherence tomography angiography (OCTA) parameters did not predict visual outcomes.
Area of Science:
- Ophthalmology
- Medical Imaging
- Retinal Diseases
Background:
- Diabetic macular edema (DME) is a leading cause of vision loss in diabetic patients.
- Intravitreal anti-vascular endothelial growth factor (anti-VEGF) therapy is a standard treatment for DME.
- Optical coherence tomography angiography (OCTA) allows non-invasive visualization of retinal vasculature.
Purpose of the Study:
- To quantify changes in OCTA parameters after anti-VEGF treatment for DME.
- To assess the association between baseline OCTA parameters and visual outcomes in DME patients.
Main Methods:
- Prospective cohort study of 29 patients with DME receiving aflibercept injections.
- OCTA imaging performed at baseline and 6 months to analyze foveal avascular zone (FAZ) and vessel density.
- Statistical analysis included Wilcoxon signed-rank test and multivariable regression.
Main Results:
- A significant decrease in superficial vascular plexus density was observed in central and inner Early Treatment of Diabetic Retinopathy Study (ETDRS) map regions, particularly in treatment responders.
- No significant association was found between pretreatment OCTA parameters and final visual acuity outcomes.
Conclusions:
- Intravitreal aflibercept treatment leads to reduced superficial vessel density in responders, potentially due to OCTA technology limitations.
- Pretreatment OCTA parameters are not reliable biomarkers for predicting visual outcomes in DME patients treated with anti-VEGF therapy.
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