Keys Flashcards

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1
Q

What are the clinical features of Von Hippel Lindau Syndrome?

A

(1) Retinal capillary haemangiomas (multiple, bilateral) – proliferating endothelial cells forming primitive capillary networks
(2) CNS haemangioblastoma
(3) Phaeochromocytoma
(4) Renal cell carcinoma
(5) Cysts of kidneys, liver, pancreas, epididymis, ovaries, lungs

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2
Q

What are the features and likely sources for different retinal emboli?

A

(1) Cholesterol (Hollenhorst): carotid artery ICA/CCA, located in branching points, golden/refractile
(2) Platelet-fibrin: large vessel atherosclerosis, multiple, dull grey
(3) Calcific: diseased cardiac valves, single, close to disc, chalky white

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3
Q

List causes of cotton wool spots.

A

GCA; DM; HT; CRAO; CRVO; Radiation; HIV; HepC; SLE; Wegerner’s; PAN; Lyme; Toxo; Mucormycosis

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4
Q

List causes of Roth Spots.

A

Leukaemia; Septic chorioretinitis; DM; Pernicious anaemia; SLE; scurvy; sickle cell

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5
Q

List causes of NVI.

A

DM; CRVO; CRAO; OIS; Chronic RRD; Chronic Uveitis; Radiation; Tumour (Rb); Trauma (surgery);

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6
Q

List causes for nyctolopia.

A

Refractive error (myopia); glaucoma; small pupil; RP; CSNB; phenothiazines; Vit A deficiency; choroideremia

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7
Q

What are the clinical features of Refsum Disease and how is it treated?

A

FEATURES: RP; ichtyosis; anosmia; deafness; neuropathy/ataxia; mental retardation; cerebellar ataxia
TREATMENT: Restricting phytanic acid (found in animal fats/milk)

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8
Q

Outline the clinical findings for hypertensive eye disease.

A

(1) Retinopathy
(2) Choroidopathy (Elschnig spots, Siegrist streak, exudative RD)
(3) Papillopathy (Disc swelling)
(4) Ancillary (Macroaneurysm, AION, motor palsies, RVO)

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9
Q

Compare Choroidaemia to Gyrate Atrophy.

A

(1) Choroideremia - XLR – CHM gene; degeneration of choroid, RPE and photoreceptors
(2) Gyrate Atrophy - AR – ornithine aminotransferase deficiency; (↑ ornithine levels) scalloped atrophic areas

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10
Q

List causes for Choroidal folds.

A

Idiopathic, hypermetropia, retrobulbar mass, choroidal mass, posterior scleritis, uveitis, IOIS, TED, Hypotony, papilloedema, meds: Diamox, topiramate.

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11
Q

What are the causes for toxic retinopathy?

A

(1) Chloroquine >3.5mg/kg/D, Hydroxychloro >6.5mg/kg/D. Screen pre-Rx, yrly vs 5yrs (near VA; red on black Amsler; 10-2; mfERG)
(2) Vigabatrin- binasal defects, normal retina. Baseline, then r/v 6/12 1st 3 years, then yearly
(3) Thioridazine (>1g/day toxic, usual 2g/day toxic usual retina
(6) Tamoxifen (toxic>180mg/day for 1 year, usual<40mg/day)→crystalline maculopathy, vortex, CMO, optic neuritis.
Other crystalline (canthaxanthine, methoxyflurane→oxalosis, nitrofurantoin)

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12
Q

What are the causes of a crystalline retinopathy?

A
  • Talc, Canthaxanthine, Tamoxifen; Oxalosis, Methoxyflurane; Bietti’s crystalline dystrophy, calcified drusen, AD crystalline dystrophy
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13
Q

What are the causes of a bull’s eye maculopathy?

A

COMMON: Chloroquine, Clofazimine, Stargardt’s, Cone-Rod Dystrophy,
LESS COMMON: Benign Concentric Annular dystrophy; LCA; Bardet-Biedl; AD cerebroataxia; lipofuscinosis (Battens)

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14
Q

What are the tests for thrombophilia?

A

APTT; Fibrinogen; Factor V; Protein C & S; Antithrombin III; Anticardiolipin; Lupus Anticoagulant; Homocysteine; plasminogen

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15
Q

What are the intravitreal doses of Avastin, Lucentis and IVTA?

A

Avastin - 1.25 mg in 0.15ml
Lucentis - 0.3mg in 0.3ml
IVTA - 4mg in 0.1ml

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16
Q

Outline your screening regimens for DR?

A
None: At least 2 yearly
Minimal NPDR: At least yearly
Moderate NPDR: At least 6 monthly
Severe NPDR: At least 2-4 monthly
PDR: Prompt PRP
17
Q

When would you consider PRP for severe NPDR?

A

(1) Poor follow-up compliance (particularly if T2DM)
(2) Severe disease in the other eye
(3) Impending cataract surgery
(4) Evidence of retinopathy progression
(5) Renal disease
(6) Pregnancy

18
Q

What are the Laser settings for PRP?

A

(!) 500 μm retinal spot size

(2) 0.2s
(3) Power: start 200mW with moderate burn (4) Green laser
(5) 1200-1600 burns; half burn width apart; from posterior pole to equator, 2DD from fovea to equator
(6) Over 3 session spacing 1-2/52 in between
(7) Review 2-4/12 post
(8) Gonio for NVA/NVI

19
Q

What are the laser settings for treating Diabetic Macular Oedema?

A

(1) 50-100 μm
(2) Focal/grid macular laser to areas of focal leak(thickening) & capillary non-perfusion.
(3) 0.1 s or less
(4) Power: start 50 mW and go up: whitening/ darkening of MA, light burn for grid/barely visible; green (red an option)
(5) Lens: A. centralis or Goldmann
(6) Avoid confluent Rx 700 μm from centre - more conservative now
(7) Review within 3/12 retreat in 4/12
STUDIES:
• ETDRS Macular Laser: 500 μm from centre, 300 μm if VA worse than 6/12, FAZ intact,
• ETDRS Focal treatment: Direct treatment of all leaking MA between 500-3000μm from the centre
• ETDRS Grid pattern: Treat areas of diffuse leakage and/or capillary drop-out more than 500 μm from centre

20
Q

How do you increase the burn intensity?

A
  • ↑ power
  • ↑ duration (least likely of the three factors to rupture Bruchs’, but most painful)
  • ↓ spot size (concentrates laser dose)
21
Q

List some indications for PDT?

A
  1. Choroidal haemangioma; 2. Polypoidal Disease; 3. Amelanotic melanoma; 4. Multifocal CSR; 5. Inflammatory CNV