Sample Qs 4 Flashcards

1
Q

What is Leber’s congential amaeurosis

A

Autosomal recessive
eye poking, hypermetropia, sluggish pupil, macular dysplasia but normal fundal appearance

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2
Q

What is vitreomacular adhesion

A

Normal PVD process is complicated by incomplete separation of the vitreous from the retina combined with an abnormally strong adherence of the posterior hyaloid to the ILM

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3
Q

What are subclassifications of vitreomacular adhesion?

A

Focal (<= 1500 microns)
Broad (>1500microns)
Isolated or concurrent

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4
Q

What are subclassifications of vitreomacular traction?

A

Focal (<= 1500 microns)
Broad (>1500microns)
Isolated or concurrent

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5
Q

What are subclassifications of FTMH

A

Small ( < = 250microns)
Medium (250 - 400 microns)
Large >400microns
With or without VMT
Primary or secondary

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6
Q

Macular hole epidemiology

A

2:1 women
1/10000 per year
Onset by 65

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7
Q

Gass Stages for macular hole

A

1 - no sensory retinal defect
a: small yellow foveolar spot, loss of foveal contour
b: yellow foveolar ring

2 - small (100-400microns) full thickness sensory retinal defect

3 - larger (>401 microns) full thickness sensory retinal defect with cuff of SRF and yellow deposits in base of hole

4 - complete vitreous separation

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8
Q

What would be seen on FFA

A

Window defect

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9
Q

When can medical management be used for macular hole?

A

enzymatic vitreolysis with ocriplasmin

Can relieve VMT and close stage 1/2 holes

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10
Q

What are causes of macular holes?

A

Idiopathic
Trauma
CMO
ERM VMT
RRD
Laser injury
Pathological myopia
HTN
DR

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11
Q

What is polypoidal choroidal vaculopathy?

A

A variant of wet AMD with polypoidal dilatation fo the choroidal vasculature with serosanguinous PED

Most common in Asian or African

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12
Q

What is the management for macular hole

A

ILM peel and gas
Facedown posturing for larger holes >400microns or recurrent holes

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13
Q

What are complications of macular hole repair

A

cataract
Retinal tear/detachment
Failure of closure
Late reopening of hole
Endophthalmitis

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14
Q

Which drug for preventing post-op endophthalmitis

A

Intracameral cefuroxime

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15
Q

complication of cataract surgery in patients who have had lasik for myopia

A

Hypermetropic refractive surprise as underpowered lens is used

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16
Q

What is used for intraoperative reverse pupil block

A

Second instrument to lift iris forward and allow flow to posterior and anterior chambers

17
Q

What is Fuch’s ED

A

AD or sporadic
Women 4:1
Increasing age

Primary endothelial dysfunction with NAKATPase pump failure
Accumulation of fluid

Collagen COL8a2 gene
SLC4A11

18
Q

What are clinical features of FED

A

GRadually reducing VA
Stage 1: Corneal guttata - centrally
Hassal Henle bodies)
BEaten metal appearance
Pigement on endothelium

Stage 2: stromal oedema, DM folds, epithelial bullae

Stage 3: Recurrent corneal erosions - vascular pannus, stromal haze

19
Q

What is seen on specular microscopy in FED

A

Reduced endothelial cell count
Increased average cell diameter
Reduced hexagons
Increased variation in cell size.

Pachymetry - Increased CCT

20
Q

What is treatment for FED

A

RElieve oedema - 5% NaCL, Treat OHT, Warm air blown on eyes, BCL for Bullous change

DMEK
If scarring PK

21
Q

What is preferred if there is OHT/glaucoma in FED

A

Topical beta blocker

Topical carbonic anhydrase inhibitors may induce endothelial failure

22
Q

what is CHED

A

Congenital hereditary endothelial dystrophy

Bilateral corneal oedema in healthy term neonates

AR CHED2 is more severe, severe reduced VA, amblyopia, nystagmus

AD form CHED1 - mild

Treated with PK

23
Q

What is PPCD

A

Posterior polymorphous corneal dystrophy

AD

Asymptomatic

Clusters of lines of vesicles
Diffuse haze of posterio cornea

Iridocorneal adhesion
corectopia
Glaucoma

24
Q

What is the most common conditions associated with PUK

A

Rheumatoid arthritis

25
What are features of PUK
Variable pain and redness Uni/bilateral peripheral corneal ulceration with ED and stromal thinning Associated inflammation at the limbus Sectoral/diffuse scleritis
26
What are corneal complications of RA
Marginal furrow - peripheral thinning without inflammation or loss of epithelium PUK - peripheral inflammation, epithelial loss , infiltrate and stromal loss, may perf Acute stromal keraittis Sclerosing keraittis - gradual justalimabl opacification of corneal storma bordering area of scleritis Keratolysis - stromal thinning
27
What is treatment for PIL
Lubicants Exclude infection Systemic immunosuppression - coricosteroids, methotrexate, ciclospotin Severe may require pulsed oral/IV cyclophosphamide with IVMP followed by steroid sparing agent and oral steorids Doxycyline and oral vitamin C to promote healing stromal environment Topical immunosuppression
28
What is mooren's ulcer
Rare autoimmune form of PIL Associated with hpeaittis C Elderly caucasian with unilatearl disease Aggressive bilateral disease in young Africans Peripehral ulceration Leading edge undermines the epithelium Grey infiltrate at margin Underlying stromal melt Advnaces central and circumferential No perilimbal clear zone and no associated scleritis Topical steroids Systemic immunosuppresion IFN if hep C Antibiotics, cycloplegia, globe protection, BCL and glue,