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Retinal diffusion restrictions in acute branch retinal arteriolar occlusion
Leon Alexander Danyel1, M Miszczuk2, K Villringer3
1Department of Neurology, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353, Berlin, Germany. leon.danyel@charite.de.
Scientific Reports
|October 16, 2021
Summary
Retinal diffusion restrictions (RDR) are detectable in branch retinal arteriolar occlusion (BRAO) using standard stroke diffusion-weighted imaging (DWI). While sensitivity was moderate, RDR identification is feasible with DWI MRI scans.
Area of Science:
- Ophthalmology
- Radiology
- Neuroimaging
Background:
- Branch retinal arteriolar occlusion (BRAO) is a type of retinal vascular occlusion.
- Diffusion-weighted imaging (DWI) is a standard MRI technique for stroke detection.
- Retinal diffusion restrictions (RDR) have been observed in central retinal artery occlusion.
Purpose of the Study:
- To investigate the occurrence and detectability of RDR in BRAO using standard brain DWI.
- To assess the reliability of RDR detection in BRAO.
- To compare RDR detection rates based on MRI parameters.
Main Methods:
- Retrospective cohort study evaluating 89 DWI MRI scans from 85 BRAO patients.
- Two radiologists assessed scans for RDR.
- Inter- and intra-rater reliability calculated using Kappa statistics.
- Detection rates analyzed by MRI field strength, sequence type, and time from onset.
Main Results:
- Overall sensitivity for RDR in BRAO was 46.1%, with low ADC signal in 56.1%.
- RDR localization correlated with fundoscopic retinal edema in 85% of cases.
- Inter-rater agreement was substantial (κ=0.64), and intra-rater agreement was excellent (κ=0.87).
- Detection rates trended higher on 3T vs. 1.5T MRI (53.7% vs. 34.3%).
- RDR were identified up to two weeks after visual impairment onset.
Conclusions:
- Standard stroke DWI can detect RDR in a substantial proportion of BRAO cases.
- Sensitivity and inter-rater reliability for RDR in BRAO are lower than reported for central retinal artery occlusion.
- DWI is a valuable tool for diagnosing BRAO, particularly when combined with clinical findings.

