Abstract
Purpose of Review
The goal is providing an update to the latest research surrounding optoelectronic devices, highlighting key studies and benefits and limitations of each device.
Recent Findings
The Argus II demonstrated long-term safety after a 5-year follow-up. Due to lack of tack fixation, subretinal implants appear to displace over time. PRIMA’s completed primate trial showed initial safety and potential for improved vision, resulting in ongoing clinical trials; Bionic Vision Australia developed a new 44-electrode suprachoroidal device currently in a clinical trial. Orion (cortical stimulation) is currently undergoing a clinical trial to demonstrate safety.
Summary
Devices using external camera for images are unaffected by corneal or lens opacities but disconnect eye movements from image perception, while the opposite is true for implants directly detecting light. Visual acuity provided by devices is more complicated than implant electrode density, and new devices aim to target this with innovative approaches.
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Funding
This research is funded in part by NIH Center Core Grants P30 EY001319 (Bethesda, Maryland), Research to Prevent Blindness Unrestricted Grant (New York, New York).
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Victor Wang declares no potential conflicts of interest.
Ajay E. Kuriyan reports a grant from Second Sight for a clinical trial, a grant from Genentech, and personal fees from Allergen, Genentech, Regeneron, Bausch Health, and Alimera Sciences.
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Wang, V., Kuriyan, A.E. Optoelectronic Devices for Vision Restoration. Curr Ophthalmol Rep 8, 69–77 (2020). https://doi.org/10.1007/s40135-020-00232-2
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DOI: https://doi.org/10.1007/s40135-020-00232-2