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Advances in Retinal Prosthetic Research: A Systematic Review of Engineering and Clinical Characteristics of Current Prosthetic Initiatives

机译:视网膜假肢研究进展:对当前假肢举措的工程和临床特征进行系统审查

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Purpose: To date, reviews of retinal prostheses have focused primarily on devices undergoing human trials in the Western Hemisphere and fail to capture significant advances in materials and engineering research in countries such as Japan and Korea, as well as projects in early stages of development. To address these gaps, this systematic review examines worldwide advances in retinal prosthetic research, evaluates engineering characteristics and clinical progress of contemporary device initiatives, and identifies potential directions for future research in the field of retinal prosthetics.Methods: A literature search using PubMed, Google Scholar, and IEEExplore was conducted following the PRISMA Guidelines for Systematic Review. Inclusion criteria were peer-reviewed papers demonstrating progress in human or animal trials and papers discussing the prosthetic engineering design. For each initiative, a description of the device, its engineering considerations, and recent clinical results were provided.Results: Ten prosthetic initiatives met our inclusion criteria and were organized by stimulation location. Of these initiatives, four have recently completed human trials, three are undergoing multi- or single-center human trials, and three are undergoing preclinical animal testing. Only the Argus II (FDA 2013, CE 2011) has obtained FDA approval for use in the United States; the Alpha-IMS (CE 2013) has achieved the highest visual acuity using a Landolt-C test to date and is the only device presently undergoing a multicenter clinical trial.Conclusion: Several distinct approaches to retinal stimulation have been successful in eliciting visual precepts in animals and/or humans. However, many clinical needs are still not met and engineering challenges must be addressed before a retinal prosthesis with the capability to fully and safely restore functional vision can be realized.
机译:目的:迄今为止,视网膜假肢的评论主要集中在西半球正在进行的人类试验的设备上,未能捕获日本和韩国等国家的材料和工程研究的重大进展,以及早期发展的项目。为了解决这些差距,这种系统审查审查了视网膜假肢研究的全球进步,评估了当代设备倡议的工程特征和临床进步,并确定了视网膜假药领域的未来研究的潜在方向。方法:使用PubMed的文献搜索,谷歌学者和Iee Explore按照普遍的系统审查指南进行。纳入标准是同行评审的论文,证明了讨论假肢工程设计的人或动物试验和论文的进展。对于每次倡议,提供了对设备的描述,其工程考虑和最近的临床结果。结果:十个假肢举措达到了我们的纳入标准,并通过刺激位置组织。在这些举措中,四个最近完成了人类试验,三次正在进行多或单中心的人类试验,并且三个正在进行临床前的动物测试。只有Argus II(FDA 2013,CE11)已获得美国FDA批准在美国使用; α-IMS(CE 2013)使用Landolt-C测试达到了最高的视力,并且是目前正在进行多中心临床试验的唯一设备。结论:几种不同的视网膜刺激方法都是成功的,以引发视觉戒指动物和/或人类。然而,许多临床需求仍然没有满足,并且在视网膜假体之前,必须实现完全安全恢复功能视觉的视网膜假体之前必须解决工程挑战。

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