Degeneration of Fundus Flashcards

1
Q

Myopic Macular Degeneration signs

A

Tessellated fundus, Diffused/patchy choroidal atrophy, lacquer cracks, choroidal neovascularisation, macular atrophy, scleral crescent, fuchs spot is raised

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2
Q

Myopic Macular Degeneration complications

A

Posterior staphylomas, foveal retinoschisis, cataract, glaucoma, rhegmatogenous RD

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3
Q

Myopic Macular Degeneration Management

A

Monitor progression and complications, refer to an ophthalmologist for any sight-threatening complications

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4
Q

Risk factors of AMD

A

Age >50, females, Caucasians, positive family history, smoking, obesity, hypertension, prolonged UV exposure

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5
Q

Formation of drusens

A

Accumulation of lipofuscin between Bruch’s membrane and RPE, depigmentation, and hyperpigmentation of RPE

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6
Q

Dry AMD signs and symptoms

A

Signs: Focal hyperpigmentation or atrophy of the RPE with drusen
Sharply circumscribed, areas of RPE atrophy associated with loss of choriocapillaries
Enlargement of atrophic areas

Symptoms: Gradual impairment of vision

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7
Q

Dry AMD management

A

Treatment not possible, high dose of multivitamins and antioxidant supplements, eat a nutritious diet, protect against UV, self-monitor with Amsler grid

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8
Q

Wet AMD Pathogenesis

A

Wet AMD is caused by choroidal neovascularisation which grows through defects in Bruch’s membrane. CNV is due to the imbalance between vascular endothelial growth factors and pigment epithelial derived factor. initial visual loss is due to leakage of blood and serum under neurosensory retina. Accumulation of fluid results in loss of photoreceptors and form a scar and permanent vision loss

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9
Q

Wet AMD signs and symptoms

A

Si: Hard exudates, cystoid macular oedema, intra and sub retinal haemorrhages
S: Metamorphopsia, positive scotoma, rapid blurring of central vision

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10
Q

Wet AMD signs in chronological order

A

Haemorrhagic pigment epitheliul detachment, vitreous haemorrhage, subretinal scarring, massive subretinal exudation

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11
Q

Wet AMD management

A

Refer to ophthalmologist for laser photocoagulation, photodynamic therapy, intravitreal anti-VEGF agents

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12
Q

Macular Hole pathogenesis

A

Abnormal vitreo-foveolar traction

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13
Q

Macular Hole stages

A

Stage 1a: flattening of foveal depression with xanopthyll
Stage 1b: Yellow ring with metamorphopsia and VA drop
Stage 2: small full-thickness hole less then <400um
Stage 3: full size macular hole more than >400um
Stage 4: Presence of Weiss Ring is a sign of PVD

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14
Q

Macular Hole diagnostic test and management

A

Watze-Allen test and OCT

M: refer to ophthalmologist where surgery is indicated for stage 2 and above with VA worse than 6/9

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15
Q

Central Serous Retinopathy pathogenesis

A

Disorder of the blood-retinal barrier with a localised detachment of the neurosensory retina at the macula secondary to focal RPE changes

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16
Q

Central Serous Retinopathy signs

A

Accumulation of fluid in the subretinal space, round or oval detachment of the neurosensory retina at macula

17
Q

Central Serous Retinopathy management

A

Refer for monitoring, laser photocoagulation

18
Q

Cystoid Macular Oedema pathogenesis

A

Accumulation of fluid between outer plexiform layer and inner nuclear layersw/ formation of fluid filled cyst liked changes

19
Q

Cystoid Macular Oedema signs

A

Loss of foveal depression, retinal thickening, multiple cystoid areas

20
Q

Cystoid Macular Oedema management

A

Refer to ophthalmologist for steroids and NSAIDS

21
Q

Epiretinal Membrane pathogenesis

A

Proliferation of glial cells that have gained access of the retinal surface through breaks in the inner limiting membrane

22
Q

Epiretinal Membrane signs

A

Irregular light reflex, sheen at macula, epiretinal membrane is translucent, macula pucker

23
Q

Epiretinal Membrane management

A

No treatment if VA <6/12, refer to ophthalmologist for vitrectomy and membrane peeling