Argus II, is the first FDA-approved retinal implant that helps people who have lost their vision due to a blinding genetic disease.
Retinitis pigmentosa is a group of genetic disorders that affect the retina's ability to respond to light.
The disease causes slow loss of vision, beginning with decreased night vision and loss of peripheral vision and eventually leads to blindness. There is currently no cure for retinitis pigmentosa.
The Argus II retinal prosthesis is a system in which a miniature video camera is housed in the subject's glasses and sends information to a patient-worn video processing unit where the image captured by the camera is processed into instructions which are then transmitted wirelessly to a retinal implant fitted with 60 electrodes.
In the study, eight patients wearing the retinal prosthesis were asked to identify white or metallic objects against a dark background, then were asked to identify the same objects with enhanced outlines.
The tests were done in three ways - with the retinal prosthesis turned on in a standard mode, in a scrambled mode as a positive control, and turned off as a negative control.
The results for solid object identification rose from 12.5 per cent correct with the device switched off to 32.8 per cent with the device on with 26.2 per cent correct identification when the device was scrambled.
"Despite the small sample size, statistically the results have achieved significance due to the magnitude of change in the performance of the use of the device within each subject," said Yvonne Luo, from London's Moorfields Eye Hospital NHS Foundation Trust and lead researcher on the study.
"Moreover, these subjects represent people with the most severe form of the disease," Luo said.
The Argus II is the only device currently on the market in the US and is one of several devices intended to help people suffering from this disease.
The research was presented at the Annual Meeting of the American Academy of Ophthalmology in New Orleans.
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