W2 Bionic Eye Flashcards

1
Q

List the desires vs. challenges that needed to be balanced when considering the development of the Bionic Eye

A

Desires:

  • user expectations
  • surgical ease
  • small size
  • life-long implantable
  • fast track to regulatory compliance
  • versatility (e.g. channels)
  • strong
  • flexible
  • fast implementation

Challenges:

  • human limitations
  • multiple iterations
  • difficult fabrication
  • hermetic challenge
  • existing biomaterials with associated limitations
  • more features = larger
  • stiff materials
  • compromises to strength
  • $ + collaboration
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2
Q

What are the two leading diseases of Retinal Degeneration?

A

Retinitis pigmentosa (RP) - one of the leading causes of blindness in young people. The leading cause of inherited blindness. Affects 1 in 3500 in USA. ~1.5M affected worldwide.

Age-related macular degeneration (AMD) - a leading cause of blindness in the elderly population. The leading cause of blindness in over 55’s. By 2020, it will affect 3M people in USA.

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3
Q

What do the two leading diseases of Retinal Degeneration leave behind which has potential to be harnessed in treatment?

A

Both RP and AMD leave behind a viable optic nerve

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4
Q

What is the location (of the eye) in which a Retinal Prosthesis is located?

A

Supra-choroidal space.

Substantial thinning of the choroid leads to closer placement of stimulating electrodes to target neurons.

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5
Q

What are the layers of the eye from superficial to deep?

A
Epi-retinal
Nerve fibre layer
Retinal ganglion cells
Amacrine cells
Bipolar cells
Horizontal cells
Photoreceptors
Sub-retinal
Pigment epithelium
Choroid
Supra-choroidal
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6
Q

Which cells of the eye die in RP and AMD?

A

Photoreceptors –> rods and cones.

The cells ‘above’ survive (e.g. horizontal, bipolar, amacrine, retinal ganglion), and can be electrically stimulated

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7
Q

When was the original bionic eye patented? What did the first patient report?

A

Aug. 28, 1956, as a ‘Retinal Stimulator’, a ‘supra-choroidal’ implant.

The patient reported seeing uniform white light in the region of the implant where a “great dark patch” existed prior to the operation. The patient also reported increased confidence in mobility.

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8
Q

What are alternative points of intervention in the visual pathway of the nervous system?

A

Eye –> retina, optic nerve
Lateral Geniculate Nucleus (LGN)
Visual Cortex

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9
Q

Describe the implant method of a retinal prosthesis

A

Array sits within a stable ‘pocket’.
Significantly simplified surgical approach.
Protection of neurons from stimulation by-products due to physical separation (behind choroid).
Can co-exist with residual vision (potential for AMD therapy).

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10
Q

What is the general idea for how the bionic eye should work?

A

Small, supporting electronics affixed to the surface of the globe, inductive power and data supplied from an implant placed behind the ear

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11
Q

How does the design of the Electrode Array impact the scleral wound?

A

Appropriate physical and electrochemical size of electrodes –> minimisation of the scleral wound (currently 3.1 mm)
(appropriate robustness)

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12
Q

What are some of the beneficial features of Gregg’s Bionic Eye Microelectronics?

A
  • robust safety features
  • parallel stimulation capabilities
  • focal activation via hexapolar multiplexing
  • threshold reduction through Quasi-monopolar stimulation
  • reverse telemetry
  • high compliance voltage for stimulation from the suprachoroidal space
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