Insertion of a subretinal prosthesis system for retinitis pigmentosa

Current evidence on the safety and efficacy of insertion of a subretinal prosthesis system for retinitis pigmentosa is limited in quality and quantity. Therefore, this procedure should only be used in the context of research.

NICE encourages further research on this procedure. Outcomes should include the impact on quality of life and activities of day‑to‑day living, and durability of implants. NICE may update the guidance on publication of further evidence.