AI diagnostic company IDx revealed on Tuesday that it has developed the clinically-aligned autonomous algorithms IDx-DR to identify and detect diabetic retinopathy using artificial intelligence in a growing number of diabetic patient across the US .
The company said IDx-DR, an US FDA-cleared AI system that detects diabetic retinopathy, a leading cause of blindness, now does not require a physician to interpret the images or results. the device allows patients who are at high risk for this blinding eye disease to be tested in non-eye care settings.
More than 30 million Americans have diabetes and an estimated 24,000 lose vision each year from diabetic retinopathy, a complication of diabetes. If caught in its early stages, vision loss and blindness are almost entirely preventable, yet only about half of people with diabetes get regular eye exams.
Recently, a diabetes education centre at a hospital in New Orleans, LA has adopted the company's IDx-DR to enhance their existing diabetic retinopathy detection programme. Their goal is to increase the number of patients they are able to test from 10-13 to over 20 a day.
Additionally, Madhu Mohan, MD, an endocrinologist at Riverside Medical Associates in Riverdale, MD, is now using IDx-DR to test his patients during their regularly scheduled visits, concluded the company.
Antin to acquire clinical trial equipment provider Emsere
Hyphens Pharma licenses Cerapro skin cream to Louis Widmer for six European markets
Profusa signs French distributor to expand Lumee Oxygen rollout in Europe
BrioHealth Solutions enrols 100th participant in BrioVAD System trial
Abbott's Amplatzer Piccolo Delivery System receives US FDA clearance and CE Mark
Amphix Bio announces initial closing of USD12.5m seed financing round
Bioretec wins FDA breakthrough status for biodegradable orthopaedic DrillPin
Amferia raises EUR3.5m to advance antimicrobial wound-care platform
BioCryst wins FDA approval for oral HAE prophylaxis in young children
ALR Technologies announces GluCurve Pet CGM relaunch in Canada
Galderma secures EU MDR certification for Sculptra, expanding use to multiple body areas
Clinical Laserthermia Systems applies for CE marking of ClearPoint Prism neuro laser system
Bonesupport shifts CERAMENT V review to FDA's De Novo pathway