Dr Adrian Hunt authored a feature article for miVision exploring how the Fight Retinal Blindness! (FRB!) registry goes beyond data collection to produce research that directly shapes clinical decisions for retinal patients.
The article explains how real-world outcome data — entered by ophthalmologists across Australia and internationally — is used to benchmark treatment patterns, identify where practice can improve, and generate the kind of evidence that randomised trials alone cannot provide.
Read the full article on miVision →
What this means for patients: Every injection and every review appointment at Eye Surgeons Miranda contributes data to the FRB! registry. This article explains why that matters — the data doesn’t sit in a database, it informs how retinal conditions are treated across the country, and it holds clinicians accountable to their own outcomes.