http://www.livemint.com/Opinion/ZRPkkwyacH5Tnq1QFE7EMK/The-now-and-the-next-of-Argus-II.html
bionic ocular technology seems new, its development has been under way
for over two decades. Research and experimentation on a bionic eye
began in the early 1990s at Johns Hopkins University. By 1998, this
work had demonstrated that a retinal prosthesis could use electricity
to stimulate the retina and produce spots of light visible to blind
patients. This created the potential for restoring sight in patients
with advanced retinitis pigmentosa, a rare genetic disorder afflicting
an estimated 1.5 million people worldwide. Second Sight Medical
Products Inc. was founded in California to develop this prosthesis.

The technology from which Argus II developed was a natural extension
of cochlear implant technology, though the building of miniature
electrodes in greater numbers needed to be developed from the ground
up. The research benefited from the development of cell phones and the
miniaturization of computers and cameras.

The first clinical trial began in 2002 with Argus I, a 16-electrode
implant based on an established cochlear implant platform. After
successful studies, a trial for Argus II, a 60-electrode device
designed to be smaller and easier to implant, began in 2007. The
trials were successful and Argus II has since been approved by the
Food and Drug Administration (FDA).

Argus II is approved for commercial utilization in both the US and
outside. Outside of the US, the Argus II is indicated for individuals
with severe to profound vision loss due to outer retinal degeneration.
In the US, the product label restricts the use for patients with bare
light perception or no light perception, caused specifically by the
outer retinal degenerative disease of retinitis pigmentosa.
Additionally, candidates must be aphakic, meaning they cannot have
their natural lens in place. If their natural lens has not been
previously removed in a prior cataract surgery, lens removal at the
time of implantation is required.

Argus II consists of three components; an implant that is surgically
placed on the retina, a pair of glasses with an attached camera and a
portable video processing unit (VPU). Images are captured by the
camera, processed by the VPU and then transmitted wirelessly to the
implant, which comprises an array of 60 electrodes.

The implant converts the information into a series of small electrical
pulses. The patient “sees” greyscale images—similar to how images
appear on a digital scoreboard—which they learn to interpret. An
extensive fitting period after implantation tailors the device to the
optimal level for each individual. With Argus II, users can detect
objects in their paths, or things such as doorways or the lines of a
crosswalk. Movement and objects with greater light contrast tend to be
easier to detect.

From a patient’s perspective, the device can provide a greater degree
of mobility. While they might not have “normal” sight, patients fitted
with the Argus II have demonstrated the ability to track sidewalks,
avoid obstacles, follow high-contrast lines on the ground, which in
general helps them feel safer and more confident. For many, obstacles
such as doorways and furniture no longer pose a problem and handling
objects like glasses and utensils becomes less complicated. Some
patients have even reported that activities such as archery or
basketball become possible with the aid of lights strung on the
targets.

While Argus II does not restore “normal” vision, many patients
describe looking into the night sky and locating the moon, or enjoying
Christmas lights, fireworks and even sports on television as they can
detect the movement on the screen. For many patients, regaining some
form of sight is significant because it allows them greater social
interaction, especially in being able to determine where people are
around them. Blindness can be very isolating. For those who have been
blind for many years, they get a great deal of enjoyment in
discovering what they can do with the system.

This technology is always being improved. Just like a phone or a
computer, Argus II can be updated with software upgrades to improve
the operating system. Such software developments will include
combining computer vision, independent manipulation and a user
interface to help decipher visual information, which will create a
more natural experience.

Efforts are also underway to reduce the cost of the device. Software
improvements will aid in reduced costs. This therapy may also be
expanded to include patients suffering from other forms of blindness,
firstly patients with AMD (age-related macular degeneration), the
leading cause of blindness in the western world which is estimated to
affect 20 to 25 million people worldwide.

More advances are potentially on the horizon, including the
development of the Orion Cortical Prosthesis, an implant which will
bypass the optic nerve and stimulate the visual part of brain,
allowing treatment of almost all forms of blindness.


Robert Greenberg, an expert in retinal prosthetics, is MD from John
Hopkins School of Medicine, and was formerly the lead reviewer of
medical devices for the US FDA. He is the president and CEO of Second
Sight Medical Products, which developed Argus II.


-- 
Avinash Shahi
Doctoral student at Centre for Law and Governance JNU



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