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Bionics: Seeing into the Future

By Joshua Nicholls

While the Bionic Eye might seem like a technology of the far future, exciting advancements are being made in the field of visual prostheses. This piece points a keen eye at emerging treatments for some of the most prominent diseases, along with their possible bionic treatments.

Issue 1: September 24, 2021

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Illustration by Friday Kennedy

Visual prostheses, colloquially known as bionic eyes, are a set of experimental devices designed to restore — or partially restore — vision to those with varying levels of blindness (1). While once viewed as “science fiction”, these technologies are becoming a reality for thousands of Australians with visual impairments. Since its inception in 1956 by the Australian inventor Graham Tassicker (2), the idea of restoring vision using electronics has undergone several developments, ranging from rudimentary cortical stimulation to modern advancements in state-of-the-art retinal implants.

As of 2018, it was estimated that over 13 million Australians have some form of visual impairment. Of these 13 million, 411,000 have cataracts or the clouding of the lens; 244,00 have macular degeneration, which degrades fine detail vision; and 133,000 are either partially or entirely blind (3,4).

The economic burden of blindness in Australia is substantial. In 2009, it was estimated that the total cost of vision loss per person aged 40 and over was $28,905 — a nationwide total of 16.6 billion AUD (5).

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Figure 1: Categorisation of Total Economic Cost of Vision Loss in 2009 (5)

Age-related macular degeneration (AMD) is one condition for which visual prosthetics may be applicable. AMD refers to the irreversible loss of high-acuity, colour-sensitive cone cells in the centre field of vision. This structure of the retina is responsible for reading, recognising faces, driving, and other visual tasks that require sharp focal vision. In fact, you are using these cells to read this article right now. Its typical onset is later in life, affecting 12% of people aged 80 or over (6). As the leading chronic eye condition for elderly Australians (7), it accounts for 48% of all cases of blindness nationwide (8). According to AIHW4, there is also a higher prevalence amongst females than in males — between 4.9%–6.8% and 3.6–5.1%, respectively.

Macular degeneration exists in two forms: dry and wet. Dry macular degeneration is caused by thinning of the macula; it is the most common form of the disease and progresses slowly over many years. Wet macular degeneration is a potentially more severe variation of the disease which is caused by the sudden development of leaky blood vessels around the macula (9). With no known cure — and most treatments being directed towards prevention and delaying progression — interventions relying on prosthetics may be the best hope for the restoration of lost eyesight (10).

Graham Tassicker was the first to realise the potential utility of cortical stimulation in restoring sight to those with vision loss. In 1956, Tassicker developed a photosensitive selenium cell which, when placed behind the retina, resulted in phosphene visualisation — the phenomenon of seeing light without light actually entering the eye (2). This was the first evidence of non-cortical stimulation to elicit visual experience. It was in the 1990s that visual prostheses took a radical development; sophisticated retinal surgeries and the creation of biomaterials led to a surge of novel inventions, including cortical implant miniaturisation and artificial retinas — the latter of which is the most advanced to date. 

There is currently a state-of-the-art retinal bionic system that has recently undergone clinical trial research: the Argus II Retinal Stimulation System. The Argus is an epiretinal (above the retina) implant which has been designed by SecondSight; as of 2013, it was FDA approved for retinitis pigmentosa (RP) but has potential utility for dry AMD. It consists of a device that is implanted in the patient’s eye and an external processing unit worn by the user. The system consists of sixty electrodes, each of which is two-hundred-micrometres in diameter. Images that have been captured by a small camera on glasses are converted into electrical impulses to stimulate surviving ganglion cells on the retina. It is currently the most widely used retinal prosthetic system in the world, with more than 350 RP patients being treated to date. The cost of this device is 150,000 USD — a price that excludes surgery and post-operative training (11).

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Figure 2: The design of the Argus II (12)

In 2015, a case study was performed by the Argus II study group on the impact the implant would have on restoring visual function to subjects who had complete blindness from RP. The results from this study were quite promising; it showed that of the 30 patients who received the Argus II system, all significantly performed better on a white square test than they did without the prosthesis. (None of the subjects scored any points with the device absent.) The Argus also showed reliability for 29 subjects, all of whom still had functioning devices after three years (13).

In 2020, a clinical trial of this device for dry AMD was completed. The study, which consisted of five patients, assessed the safety and feasibility of the device. According to Mills et al. (14), no patients reported confusion when operating the Argus alongside their healthy peripheral vision. Adverse events occurred in two patients who experienced proliferative vitreoretinopathy — or tractional retinal detachment.

However, due to recent events surrounding the COVID-19 pandemic, the company declared that they would be performing “an orderly wind-down of the company’s operations”. SecondSight is now focusing on a new device: The Orion. This device is designed to stimulate the visual cortex of the brain — a return to the original conception of visual prosthetics. The Orion is planned to expand the pool of patients who are eligible for visual prosthetics. It will essentially bypass the requirement for healthy ganglion cells and a functioning optic nerve, which retinal prosthetics require. The only forms of blindness not encompassed by this technique are congenital forms of blindness or people who are ‘cortically blind’ from suffering damage to the visual cortex area V1. The Orion is modelled after the Argus II with its 60 cortical-stimulating electrodes receiving input from a camera on the user’s glasses. Under the Breakthrough Device Pathway, the FDA approved Orion for an early feasibility study. Six human subjects have been fitted with the device — one woman and five men between the ages of 29 and 57. Of these six, one had endophthalmitis, two had glaucoma, and three suffered trauma. After one year of wearing the device, four of the patients could accurately discern the location of a palm-sized white square on a computer screen, and five could locate its movement in space. The Orion has shown a good safety profile after 12 months of use, and follow-ups on its progress will occur for five years (15).

Visual prostheses have a promising and bright future of development ahead of them. While it is still in its infancy, the results of ongoing clinical trials show promise for sight restoration. With multiple models and modes of intervention available, artificial vision is slowly becoming a reality for the visually impaired, but further developments in the field are still required. It would be promising to see advancements from mere two-dimensional grey-scale images to the rich, three-dimensional, and full-colour experience that we take for granted as normal vision. For now, two essential factors need to be improved for the full realisation of artificial vision: cost and electrode density. The Argus costs 150,000 USD — an expense that excludes surgery and training. This figure may be unfeasible for the thousands of Australians who would benefit from such a device. If the current trend of Moore’s Law continues, electrode density will increase whilst the cost of the device will decrease — a trend analogous to the increase in power and improved price of computers in the last century. This pixel density will hopefully improve to the point of achieving near-normal visual acuity. The 60 pixels, while helpful in regaining some functionality, cannot compare to the some 96 million photoreceptor cells in the retina — 5 million of which are located in the cone-dense macula. Nevertheless, artificial vision is an exciting and innovative technology currently under development. While much research is still needed, further advancements in bionics will one day make visual prosthetics a ubiquitous and affordable technology to those in need.

About the writer: Joshua Nicholls was the 2021 winner of the Let's Torque competition. 

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Joshua: I am a 5th-year neuroscience and biochemistry student at the Swinburne University of Technology. I finished my Health Science degree a few years ago, majoring in neuroscience. I am now completing my final few subjects in my Bachelor of Science, with biochemistry as my major.

For the state-wide Let’s torque competition, I changed my pitch to artificial vision, hence its title, Bionics: Seeing into the Future—a catchy pun, if I do say so myself. I made the rather complex topic of visual prosthetics approachable and understandable to the general audience by, as stated previously, conveying a story.

I asked my audience to consider losing vision, if not completely, at least partially. Considering this, I then asked them to imagine what life must be like for the some 13 million Australians of whom suffer from some form of visual impairment. This exercise brought home the very real phenomenon of visual impairment, which many of us have—or will—be impacted.

​The solution for currently untreatable vision loss is already underway: The Bionic Eye, as it is colloquially known. While it may sound like science fiction, bionics (or prosthetics) are nothing new; artificial hearing through the cochlear implant and artificial limbs are becoming rather ubiquitous. I briefly detailed a few diseases for which visual prosthetics may be appropriate, such as age-related macular degeneration and retinitis pigmentosa, and spoke about past and current clinical trials demonstrating their efficacy.

​To end my pitch, I talked about the lasting impact these devices will have on people’s lives and the future developments required. In doing so, I relayed the past, present, and future of the bionic eye, which detailed a coherent and relatable story to my audience. I was successful in my pitch and won first place among the state! It was an absolute privilege even to have been a part of this competition; coming first place was an added honour and will remain one of the highlights of my life.

​I believe this experience will serve as a footstone toward my career in science and science communication. If anyone has any desires to get their foot in the door of this field, get your name and face out there and just go for it!

References:

  1. Ong, J. M., & da Cruz, L. (2012). The bionic eye: a review. Clinical & experimental ophthalmology, 40(1), 6-17. 

  2. Tassicker, G. (1956). Preliminary report on a retinal stimulator. The British journal of physiological optics, 13(2), 102-105.

  3. Australian Bureau of Statistics. (2018). National Health Survey: First Results, 2017–18. Canberra: ABS Retrieved from https://www.abs.gov.au/statistics/health/health-conditions-and-risks/national-health-survey-first-results/latest-release

  4. Australian Institute of Health and Welfare. (2021). Eye health. Canberra: AIHW Retrieved from https://www.aihw.gov.au/reports/eye-health/eye-health 

  5. Taylor, P., Bilgrami, A., & Pezzullo, L. (2010). Clear focus: The economic impact of vision loss in Australia in 2009. Vision2020. Retrieved from https://www.vision2020australia.org.au/wp-content/uploads/2019/06/Access_Economics_Clear_Focus_Full_Report.pdf

  6. Mehta, S. (2015). Age-related macular degeneration. Primary Care: Clinics in Office Practice, 42(3), 377-391. 

  7. Foreman, J., Xie, J., Keel, S., van Wijngaarden, P., Sandhu, S. S., Ang, G. S., . . . Taylor, H. R. (2017). The prevalence and causes of vision loss in Indigenous and non-Indigenous Australians: the National eye health survey. Ophthalmology, 124(12), 1743-1752. 

  8. Taylor, H. R., Keeffe, J. E., Vu, H. T. V., Wang, J. J., Rochtchina, E., Mitchell, P., & Pezzullo, M. L. (2005). Vision loss in Australia. Med J Aust, 182(11), 565-568. doi:10.5694/j.1326-5377.2005.tb06815.x

  9. Calabrese, A., Bernard, J.-B., Hoffart, L., Faure, G., Barouch, F., Conrath, J., & Castet, E. (2011). Wet versus dry age-related macular degeneration in patients with central field loss: different effects on maximum reading speed. Investigative ophthalmology & visual science, 52(5), 2417-2424.

  10. Cheung, L. K., & Eaton, A. (2013). Age‐related macular degeneration. Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, 33(8), 838-855. 

  11. Luo, Y. H.-L., & Da Cruz, L. (2016). The Argus® II retinal prosthesis system. Progress in retinal and eye research, 50, 89-107. 

  12. SecondSight. (2021). SecondSight: Life in a New Light. Retrieved from https://secondsight.com/

  13. Ho, A. C., Humayun, M. S., Dorn, J. D., Da Cruz, L., Dagnelie, G., Handa, J., . . . Hafezi, F. (2015). Long-term results from an epiretinal prosthesis to restore sight to the blind. Ophthalmology, 122(8), 1547-1554. 

  14. Mills, J., Jalil, A., & Stanga, P. (2017). Electronic retinal implants and artificial vision: journey and present. Eye, 31(10), 1383-1398.

  15. Pouratian N., Yoshor D., & Greenberg R. (2019). Orion Visual Cortical Prosthesis System Early Feasibility Study: Interim Results. Paper presented at American Academy of Ophthalmology Annual Meeting.

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