A Second-Generation (44-Channel) Suprachoroidal Retinal Prosthesis: A Single-Arm Clinical Trial of Feasibility

被引:3
|
作者
Petoe, Matthew A. [1 ]
Abbott, Carla J. [2 ,3 ,4 ]
Titchener, Samuel A. [1 ]
Kolic, Maria [3 ]
Kentler, William G. [5 ]
Nayagam, David A. X. [1 ,3 ,6 ]
Baglin, Elizabeth K. [3 ]
Kvansakul, Jessica [1 ]
Barnes, Nick [7 ]
Walker, Janine G. [7 ,8 ]
Karapanos, Lewis [3 ,4 ,9 ]
McGuinness, Myra B. [3 ,4 ]
Ayton, Lauren N. [3 ,4 ]
Luu, Chi D. [3 ,4 ]
Allen, Penelope J. [3 ,4 ,10 ]
机构
[1] Bion Inst, Melbourne, Vic, Australia
[2] Univ Melbourne, Med Dept Bion, Melbourne, Vic, Australia
[3] Royal Victorian Eye & Ear Hosp, Ctr Eye Res Australia, Melbourne, Vic, Australia
[4] Univ Melbourne, Dept Surg, Ophthalmol, Melbourne, Vic, Australia
[5] Univ Melbourne, Dept Biomed Engn, Melbourne, Vic, Australia
[6] Univ Melbourne, St Vincents Hosp, Dept Pathol, Melbourne, Vic, Australia
[7] Australian Natl Univ, Res Sch Engn, Canberra, ACT, Australia
[8] CSIRO, Hlth & Biosecur, Canberra, ACT, Australia
[9] Univ Melbourne, Dept Optometry & Vis Sci, Melbourne, Australia
[10] Royal Victorian Eye & Ear Hosp, Vitreoretinal Unit, Melbourne, Australia
来源
OPHTHALMOLOGY SCIENCE | 2025年 / 5卷 / 01期
基金
英国医学研究理事会;
关键词
Suprachoroidal retinal prosthesis; Functional vision; Bionic eye; Retinitis; pigmentosa; QUALITY-OF-LIFE; FUNCTIONAL VISION; BLIND SUBJECTS; VISUAL PERFORMANCE; SYSTEM; PART;
D O I
10.1016/j.xops.2024.100525
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To assess the feasibility of a second-generation (44-channel) suprachoroidal retinal prosthesis for provision of functional vision in recipients with end-stage retinitis pigmentosa (RP) over 2.7 years. Design: Prospective, single-arm, unmasked interventional clinical trial. Participants: Four participants, with advanced RP and bare-light perception vision. Methods: The 44-channel suprachoroidal retinal prosthesis was implanted in the worse-seeing eye. Device stability, functionality, and adverse events were investigated at approximately 12-week intervals up to 140 weeks (2.7 years) postdevice activation. Main Outcome Measures: Serious adverse event (SAE) reporting, visual response outcomes, functional vision outcomes, and quality-of-life outcomes. Results: All 4 participants (aged 39-66 years, 3 males) were successfully implanted in 2018, and there were no device-related SAEs over the duration of the study. A mild postoperative subretinal hemorrhage was detected in 2 recipients, which cleared spontaneously within 2 weeks. OCT confirmed device stability and position under the macula. Improvements in localization abilities were demonstrated for all 4 participants in screen-based, tabletop, and orientation and mobility tasks. In addition, 3 of 4 participants recorded improvements in motion discrimination and 2 of 4 participants recorded substantial improvements in spatial discrimination and identification of tabletop objects. Participants reported their unsupervised use of the device included exploring new environments, detecting people, and safely navigating around obstacles. A positive effect of the implant on participants' daily lives in their local environments was confirmed by an orientation and mobility assessor and participant self-report. Emotional well-being was not impacted by device implantation or usage. Conclusions: The completed clinical study demonstrates that the suprachoroidal prosthesis raises no safety concerns and provides improvements in functional vision, activities of daily living, and observer-rated quality of life. (c) 2024 by the American Academy of Ophthalmology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
引用
收藏
页数:17
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