Optomed Aurora with AEYE-DS is the only FDA-cleared handheld AI fundus camera. Recent clinical trials demonstrated that the Optomed Aurora AEYE handheld camera exhibits diagnostic sensitivity was in the range of 92%-93% and specificity was in the range of 89%-94%. In both studies, over 99% of patients received a diagnostic result. Its non-mydriatic and single image per eye operation offers quick and accurate screening. Its high-contrast optical design is engineered to detect small early-phase retinal changes with a 50-degree field-of-view. The ease-of-use is further increased by autofocus and auto exposure functions. It has the capability to capture digital images that can easily be sent to eye care providers.
Nearly 50% of the 38.4 million Americans who have diabetes skip their annual eye exams, leaving them vulnerable to diabetic retinopathy and blindness. Autonomous screening in primary care can improve clinic adherence to HEDIS measurements, is reimbursable, and ultimately can prevent blindness in diabetics at risk for vision loss.
“The Optomed Aurora AEYE gives primary care providers the opportunity to bridge the diabetic retinopathy gap in the US with immediate, on-the-spot detection of diabetic retinopathy with results in about 60 seconds,” said David Frasch, Managing Director. “This technology removes the guesswork out of when it is necessary to refer a patient to an eye care provider. Results with the Optomed Aurora AEYE are simple: red means you refer to an eye care specialist, and green means you screen again in 12 months.”
