W11 AMD Flashcards

1
Q

Photoreceptor structure:

A

PR outer segments: Discs of pigment (opsins bound chromophore 11 cis-retinal)
Inner segments: ^mitochondria for great metabolic consumption

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2
Q

RPE functions:

A

Transport from choroid/Retina
Tight junctions prevent passive diffusion from choroid
Melanin absorbs light (protect)
Phago. Outer seg. (PR debris)
Produces FGF, PDGF, VEGF, PEDF

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3
Q

RPE outflow/influx:

A

Influx
Glucose (energy), omega 3 (OS structure), amino/ascorbic acid
Outflow
Water, ions, metabolic EP’s

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4
Q

Bruchs membrane:

A

“BrMb” 3um connective tissue between RPE/choriocapillaris (nut. Source)
ECM of elastin/collagen fibres
Regulates ion/antioxidant transport

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4
Q

Choriocapillaris (CC)

A

Capillaries posterior to bruchs membrane
Proximity allows transport for metabolic PRs (O2)

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5
Q

AMD simple patho:

A

Oxidative/age related damage to PRs/RPE/Bruch’s/Choriocapiliaries
Loss of PRRPEBrMbCC complex symbiotic relationship results in macula degeneration

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5
Q

AMD patho for bruchs dysfunction:

A

Progression > soft drusen (>67um) > ^size/confluent > thickening/calcification/degeneration of elastin/collagen layers of bruchs > hydrophobic barrier to fluid/nut. > loss between outer retina/choroid

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6
Q

AMD patho for atrophic/non-exudative:

A

RPE loss > PR/CC dysfunction > largening chorioretinal geographic atrophy
RPE-produced trophic factor (VEGF) loss > CC atrophy > altered perfusion of choroidal vessels

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6
Q

AMD patho for drusen formation:

A

Age/oxidation > dysfunctional metabolism of rod OS (^at macula) > ^metabolic by-products:
Basal laminar deposit (RPE/basement): collage (cell stress)
Basal linear deposit (inner portion of bruchs): lipid/lippofuscin/complement (soft drusen; pro-inflammatory)

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7
Q

AMD patho for RPE loss:

A

Nutrient loss/lipofuscin tox > RPE ischemia > ^dysfunction > apoptosis (seen as hypo/hyperpigmentation)

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8
Q

Exudative AMD description/causes:

A

10% cases
PR/RPE/BrMb/CC complex insulted by stenosis of choroidal BV, pro-inflammatory response from drusen (CC toxicity)
CC loss > loss of debris exocytosis > drusen formation
Serum leak via lack of tight junctions in ne BV

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8
Q

AMD patho for neovascular/exudative:

A

PR/RPE/BrMb/CC complex insulted via loss of choroidal vasculature/perfusion > RPE hypoxia > angiogenic compound production (VEGF) > BV growth stimulation in CC > neovascular membrane (CNV) breaking bruchs > serum leak > PR loss

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9
Q

Non-exudative AMD description:

A

90% cases
Initial RPE hyperpigment, large confluent drusen
Followed drusen reabsorbtion > RPE death > hypopigment
End stage of geographic atrophy

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10
Q

Causes and risk factors of AMD:

A

Age: loss of antioxidant mechanisms
UV(long wavelength): ^free radicals > phototoxicity > cell damage
Genetic: chromosome 1q32 for complement factor H (protective factor)
Smoking: double risk from free radicals
^BMI, HT (^BMI), Cat Sx, female, hyperopia

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11
Q

Dry AMD symptoms:

A

Bilateral assymetrical gradual loss of central vision
Metamorphopsia (Drusen > PR displacement)
Central scotoma (geographic atrophy)

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12
Q

Early AMD clinical presentation/signs:

A

Sub-RPE basal linear deposits
Large soft drusen
Hyper/hypopigmentation
RPE/retina atrophy (w/drusen)
Geographic atrophy > visible choroid (wo/drusen)
PED from poor fluid transport (bruchs dysfunction) filled with serous fluid/haemorrhage/drusen

13
Q

Exudative AMD clinical presentation/signs:

A

CNV: yellow central dome elevation w/PED
Haemorrhagic PED: dark sub-RPE dome > vit-haem
Fibrovascular disciform scar: healed CNV > white patch (permeant blur)

14
Q

Exudative AMD symptoms:

A

Painless blurring central vision (in days)
Metamorphopsia/scotoma
Sudden vision loss (vit. Haem.)

15
Q

Amsler grid:

A

Qualitative 20(deg) in place of 10-2
Screens mac. Oedema, drusen, CNV, hole/traction
Viewed 30cm, each 5mm square subtends 1(deg)
Note missing area (scotoma), or warping

16
Q

Carotid artery to eye:

A

Passing cavernous sinus > splits ophthalmic artery > optic canal w/ON > branches central retinal/ciliary artery
CRA pierces ON > supply ant. Retina
Ciliary artery forms 2 long / 20 short CA’s > circle of Zinn-Haller (ON/sclera/choroid)

16
Q

FFA tools:

A

Sodium fluroescein: water soluble dye, peak excitation 490nm (blue), emits 520nm (yellow/green)
Yellow/green filter (530nm) blocks blue reflection
80% dye binds serum protein (unbound > renal/hepatic met. Removed by 36h)

17
Q

OCT description:

A

Short coherence light beam split:
Sampling beam > retina
Reference beam > mirror
Wavelength/intensity difference forms image via fourier analysis

18
Q

Phases of FFA:

A

Choroidal: 10s, fluro blocked by RPE
Arterial: 1s after, arteries hyperfluro.
Arteriovenous (capillary): complete artery filling, early laminar flow (thin vein)
Venous: 25s, artery/vein fill
Late: decreaing intensity per circulation

18
Q

BRB:

A

Outer: RPE TJs
Inner: Endo. Retinal BV TJs

18
Q

OCT AMD analysis:

A

Hyper/hyporeflection: pigment/hypertrophy of RPE/scar
Drusen
Atrophy
CNV > cystic serous spaces

19
Q

Dry AMD treatment:

A

AREDS based “macu-vision plus” supps.
Amsler, OCT, Education
Cease smoking
Refer to royal society of the blind

19
Q

Exudative AMD treatment:

A

Anti-VEGF is standard
Photodynamic/photocoagulation damage retina even with laser activated drugs

19
Q

Ranibizumab:

A

Monoclonal antibody segment against VEGF-A, binds and inhibits VEGFR of all VEGF isoforms
ANCHOR study > ^letter gain over PDT

20
Q

Anti-VEGF drugs:

A

Ranibizumab (Lucentis)
Bevacizumab (Avastin)
Aflibercept (Eylea)
Faricimab (Abysmo)

20
Q

Bevacizumab:

A

Monoclonal antibody against VEGF-A, originally systemic treatment
No significant difference in clinical efficiancy
Australia Lucentis is cheaper now (under PBS)