Elsevier

Survey of Ophthalmology

Volume 47, Issue 4, July–August 2002, Pages 335-356
Survey of Ophthalmology

Major review
Retinal Prosthesis for the Blind

https://doi.org/10.1016/S0039-6257(02)00311-9Get rights and content

Abstract

Most of current concepts for a visual prosthesis are based on neuronal electrical stimulation at different locations along the visual pathways within the central nervous system. The different designs of visual prostheses are named according to their locations (i.e., cortical, optic nerve, subretinal, and epiretinal). Visual loss caused by outer retinal degeneration in diseases such as retinitis pigmentosa or age-related macular degeneration can be reversed by electrical stimulation of the retina or the optic nerve (retinal or optic nerve prostheses, respectively). On the other hand, visual loss caused by inner or whole thickness retinal diseases, eye loss, optic nerve diseases (tumors, ischemia, inflammatory processes etc.), or diseases of the central nervous system (not including diseases of the primary and secondary visual cortices) can be reversed by a cortical visual prosthesis. The intent of this article is to provide an overview of current and future concepts of retinal and optic nerve prostheses. This article will begin with general considerations that are related to all or most of visual prostheses and then concentrate on the retinal and optic nerve designs. The authors believe that the field has grown beyond the scope of a single article so cortical prostheses will be described only because of their direct effect on the concept and technical development of the other prostheses, and this will be done in a more general and historic perspective..

Section snippets

Psychophysical Experiments

There is a general consensus that electrical stimulation of the visual pathways via a small number of electrodes cannot be expected to provide unaided understanding of visual information. In an effort to define the minimum acceptable resolution for useful vision, several psychophysical experiments were performed. As early as 1965, it was suggested that 600 points of stimulation (pixels) would be sufficient for reading ordinary print.14 Others suggested that 80–120 points are sufficient for

Surface cortical electrodes

One of the earliest experiments included three blind patients, two of whom were able to locate a light source by scanning the visual field with a photocell. The photocell output electrically stimulated the cortex via electrodes in a wire passing through the scalp and skull and penetrating the visual cortex.25

Brindley and Lewin performed key experiments in this field by implanting devices consisting of 80 electrodes on the visual cortex of blind patients (Fig. 1). Wires through a burr hole

Retinal Prostheses

During the early seventies it became clear that blind humans can also perceive electrically elicited phosphenes in response to ocular stimulation, with a contact lens as a stimulating electrode.107, 108, 109 When obtainable, these electrically elicited responses indicated the presence of at least some functioning inner retinal cells. Because a number of blinding retinal diseases are due predominantly to outer retinal (in particular photoreceptor) degeneration,72, 127, 142 the idea of

Optic Nerve Prostheses

Investigators have also stimulated the optic nerve.133, 134, 153 The optic nerve is a compact compartment of ganglion cell axons running from the retina and synapse on the lateral geniculate body. This condensed cable can be reached surgically, and theoretically has a good location for implanting a surface or penetrating stimulation electrode array. However, the high density of the axons (1.2 million within a 2 mm-diameter cylindrical structure) could make it difficult to achieve focal

Sensory Substitution Devices

As an alternative to direct stimulation of the visual system neurons, several other approaches have attempted to convert visual information into vibro-tactile or auditory signals (i.e., sensory substitution devices12, 115). The distinct advantage of these approaches is that the device is wearable and not implantable. However, these devices have never reached widespread acceptance because they do not restore the sensation of vision, have low resolution, occupy another sensory modality, can evoke

Summary

The three levels of hierarchy in the sensory systems (i.e., receptor organ, sensory pathways, and perception) suggest a similar architecture for artificial and prosthetic sensory systems. Accordingly, artificial systems should include a transducer corresponding to the receptor organ, an encoder corresponding to the sensory processing system, and finally an interpreter corresponding to perceptual functions. In other words, the visual environment will be captured and processed by a photosensing

Method of Literature Search

A literature search of the PubMed data was performed (1966–present). The following key words were used: artificial vision, blindness, cortical prosthesis, electrical stimulation electronic implants, macular degeneration, optic nerve, optic nerve prosthesis, retina, retinal prosthesis, retinitis pigmentosa, visual cortex and visual prosthesis. In addtion, some abstracts from relevant recent conferences and annual meetings were reviewed. The search was not limited to English language, but only

Outline

I. General considerations

A. Efficacy of a visual prosthesis

1. Psychophysical experiments

2. Neuronal electrical excitation

a. Threshold parameters for electrical stimulation

3. Electrodes

4. Power supply

B. Safety of electrical stimulation

1. Damage caused by electrical current

2. Infection and inflammation

3. Heat damage

4. Hermetic sealing of the electronics

II. Cortical prosthesis

A. Surface cortical electrodes

B. Intracortical microstimulation

III. Retinal prostheses

A. Epiretinal prostheses

1. In vitro

Acknowledgements

The manuscript was supported in part by grants from the National Science Foundation #BES9810914, National Eye Institute #R209EY11888, Second Sight/NIH-NEI #R24EY12893-01, Foundation Fighting Blindness, Defense Advanced Research Projects Agency, Office of Naval Research: Tissue Based Biosensors Program, The Whitaker Foundation, and The Alfred E. Mann Fund at the Applied Physics Laboratory. The authors wish to thank Rhonda Grebe, Terry Shelley, Salvatore A. D'Anna, and Devon C. Ginther, for their

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