Week 1.07 AMD Flashcards

1
Q

What are the structures within the macula

A

Macula - widest possible region
Fovea - similar size to optic nerve head
Foveola- photoreceptor cells
Umbo - light reflex in opthalmoscope

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2
Q

What is the size of the macula

A

Approx 5.5mm

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3
Q

Why is the macula darker than the rest of the retina

A

RPE cells taller and contain more pigment here than elsewhere

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4
Q

What are the yellow hue pigments in the macula

A
  • Lutein & zeaxanthin concentration greatest here – thought to play a protective role – highly metabolic active tissue so really susceptible to damage
  • Absorb short light
  • Protection from UV damage
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5
Q

What is the fovea

A

• 1.5mm diameter
• Highest conc of cones
• Shrinking down and thinning of the retina in this region
• Depression created by sweeping of neurons
• Floor of this depression = foveola
• Cones only in central 0.57mm
• Bordered by para-fovea region then peri-fovea

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6
Q

What is the function of the RPE

A

Transportation of nutrients to the PR & phagocytosis of PR outer segment

o Lipofusion is produced during this process – really important aging pigment, build up of lipofusion tells you which areas on the back of the eye are affected
• Loss of RPE causes death of photoreceptors and loss of vision

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7
Q

Burch’s membrane

A

2 to 4 micrometres thick
Thickens with age - waste products usually transported across so if gets thick that stops it from doing this

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8
Q

How does the retina age

A

• Bruchs membrane thickens
• RPE metabolism becomes inefficient
• allowing waste products build up in RPE cells – lipofusion
• Collagen / lipid deposit on bruchs membrane
= drusen – yellow dots on back of eye in macula diseases

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9
Q

What’s the main reason drusen forms

A

Thickening of bruchs membrane so drusen forms between RPE and bruchs membrane

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10
Q

What are the 2 types of drusen

A

Soft - typically bigger
Hard - typically smaller

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11
Q

Hard drusen

A

Small scattered
Yellow
Round
Well defined
Normal ageing process

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12
Q

Soft drusen

A

Larger and less well defined
Overlying RPE changes soften appearance - RPE detachment

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13
Q

Confluent drusen

A

Soft drusen that gradually coalesces
Increases risk of AMD

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14
Q

How to differentiate between exudates and drusen

A

Exudate is more brighter and easier to see, more superficial in the retina. Closer to the optom

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15
Q

What’s the difference between exudates and hard drusen

A

Exudates are intraretinal and hard drusen is subretinal
Exudates are ring patterns, hard drusen random pattern
Exudates - vascular changes (microaneurysms, dot and blot haemorrhage, cotton wool spots)
hard drusen - no vascular changes

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16
Q

Two main types of AMD

A

Dry - 90% of cases - 10% cases causing blindness
Wet - 10% of cases - 90% cause blindness

Dry - untreatable
Wet - treatable if URGENT referral

Dry is slowly progressing
Wet quickly progressing

17
Q

Dry AMD

A

Geographic atrophy - Choroidal blood vessels are visible. Very few or no photoreceptors in this area

18
Q

What happens in wet amd

A
  • Things start in the same way as the dry type
  • Brunch’s membrane thickens
  • Drusen forms
  • RPE detachment occurs
  • New vessels grow out from the choroid
  • Leakage and haemorrhage occur – causes blood to leak into the retina
  • Scarring without treatment
19
Q

What is Choroidal neovascularisation

A

New blood vessels growing up from choroid through spilts in bruchs membrane into the retina. Start to leak and disrupt photoreceptors.

Also known as choroidal neovascularisation – new blood vessels from choroid although there can be other causes of this such as high myopia, other conditions where u get splits in the retina.

20
Q

What are the risk factors for AMD

A

Older age
Presence of AMD in the other eye
FH of AMD
Smoking
Hypertension
High BMI
Diet low in omega 3 and 6, vitamins
Edit high in fat
Lack of exercise

21
Q

How to investigate AMD

A

Case hx - sxs
VA
Amsler grid
Volk
Maddox rod
Photo stress recovery test
OCT
FFA (hospital)

22
Q

What might a person with AMD say in case hx

A

Distortion especially centrally
Reduced reading vision
Shimmering
Difficulty recognising faces
Central scotoma
Family history
AMD in other eye

23
Q

Amsler chart

A
  • Chart at 30cms
  • Wearing appropriate reading spectacles (+3.25 add)
  • Occlude each eye individually
  • Full room illumination
  • Covers central 20 degrees – 10 degrees either side of fixation
24
Q

Maddox rod

A

Px may report breaks or distortion in the image

25
Q

Photo stress recovery test

A

Basically bleaching vision and then checking how long it takes for vision to come back

Measure DV VA
Occlude one eye
Look light 10 secs
Replace specs back on
Direct px to line above VA
Ask them to read line immediately the after image disappears
Time how long it takes for px top read 2/3rd of line correctly
Repeat for other eye if necessary

Normal recovery 0-30 seconds
30-60 seconds possible maculopathy not definite
>60 seconds maculopathy

26
Q

What is shown in late AMD

A

Scare tissue

27
Q

How to manage dry amd

A

Monitor and be aware wet could develop
Counsel
Advice
Refer

Eat foods that contain more leutein and zeaxanthin - kale, sweetcorn, orange, peppers, eggs

28
Q

How to manage wet AMD

A

Urgent referral from primary care within 2 weeks
Anti-VEGF injections
Smoking advice
Registration - blind

29
Q

What is the NICE guidelines for referral of amd

A

In order for eye to be treated:
- Best corrected VA between 6/12 and 6/96
- no permanent structural damage to central fovea
- lesion size is less than or equal to 12 disc areas in greatest linear dimension