Sample Qs 3 Flashcards

1
Q

What is ERG

What is the method?

A

ERF records mass electrical activity from retina stimulated by flash of light

Full field simulation
Electrodes corneal contact/bulbar conj

Rod response in DA eyes (after 30 mins in dark) with dim white flash below cone sensitvity and b wave only

Maximal ERG - DA eyes using bright white flash - mixed rod and cone repsonse

Photopic response - background that surpresses rod acctivity and single flash cone response in light adapted eyes (after 10 mins in light(

Cone derived flicker using 30Hz white light flicker

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2
Q

Where to ERG a waves come from? b waves? Oscillatory potentials

A

a - photoreceptors
b - bipolar and Mullar cells
OP - amacrine cells

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3
Q

How do ischaemic and non-ischaemic CRVO differentiated on ERG

A

b wave affected by large areas of ischaemia
Reduced b amplitude
Reduced b:a wave ratio
Prolonged b wave implicit time

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4
Q

What is the ERG change in achromatopsia

A

Abnormal photopic and normal scotopic ERG
Absent flicker

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5
Q

What is the ERG change in CSNB

A

Normal a wave, reduced scotopic b wave

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6
Q

What conditions have reduced a and b waves on ERG

A

Rod/cone dystrophy
Total RD
Metallosis
Drug toxicity
Autoimmune retinoapthy
CAR
Ophtahlmic artery occlusion

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7
Q

What conditions have normal a and reduced scotpic b waves on ERG

A

CSNB
XL retinoschiasis
CRAO CRVO
Myotonic dystrophy
Melanoma associated retinopathy
Quinine tox

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8
Q

What gives reduced oscillatory potentials on ERG

A

Drug tox - vigabatrin

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9
Q

What is achromatopsia

A

Rod monochromatism

Autosomal recessive

Lack of cone function of all 3 subtypes

Poor VA and CV from birth
Pendular nystagmus
Photophobia

Normal fundus

ERG: reduced photopic, normal scotopis -

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10
Q

What is CSNB

A

Early non progressive nyctalopia

Associated with reduced VA, refractive error (myopia commonly), nystagmus, strabismus

Normal fundus vs abnomral fundus

Mutations in NYX GRM6 TPRM1

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11
Q

What ERG abnormalities in CSNB

A

Complete CSNB - no dtectable rod ERG, electronegative bright flash response - reduced b wave to a wave ratio - inner retinal dysfunction

incomplete CSNB - detectable rod specifc ERG and negative bright flash response
cones more abnormal than in cCSNB

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12
Q

What are risk factors for ROP

A

Low gestational age (<32 weeks)
Low birth weight (<1500g)
High or variable oxygen tension

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13
Q

What are ROP Stages ICROP

A

Stage 1 - demarcation line - flat white line separating vascular from avascular zones

Stage 2 - ridge - line becomes elevated and thickened, may become pinkish with neovascular tufts posterior to ridge

Stage 3 - ridge with extraretinal fibrovascular proliferation - vascular tissue grows from posterior margin on to retina or into vitreous

Stage 4 subtotal retinal deteachment - extrafoveal 4A or foveal 4B

Stage 5 - total RD

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14
Q

What is plus disease

A

Significant venous dilatation and arteriolar tortuosity
(compared with standard photo)
of the posterior retinal vessels in two or more quadrants

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15
Q

What is pre-plus disease

A

There is more venous dilatation and arteriolar tortuosity than normal but insufficient to be plus disease

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16
Q

What are zones of ROP

A

Zone I - circle centered on disc with radius twice the distance from the centre of the disc to the fovea

Zone II - ring centered on the disc, extending from zone 1 to the ora nasally and the equator temporally

Zone III - remaining temporal crescent

17
Q

What is threshold disease?

A

Stage 3 ROP WITH
Plus disease in zone I or II
AND OF
5 continuous or 8 non-continuous hours of disease

18
Q

What babies must be screened for ROP

A

<31 week gestational age
<1251g birthweight

19
Q

When is the first screening examination

A

Babies born <27wks - 30-31 wk post-menstrual age

Babies born between 27 and 32 weeks
4-5 week postnatal age

> > 32 wk gestational age but < 1501g weight
4-5 wk postnatal age

20
Q

How frequently to screen if vessels end in zone 1 or posterior zone 2

21
Q

How frequent to screen plus or pre-plus or stage 3 disease

22
Q

When can you terminate screening in babies with no ROP

A

Vascularization has extended into zone III - 36 completed weeks post-menstrual age

23
Q

When can you terminate screening in babies with ROP no requiring treatment

A

2 successive exams showing:
Lack of increase in severity
Partial resolution
Change in colour in ridge from salmon pink to white
Transgression of vessels through the demarcation line
Commencement of the process of replacement of active ROP lesions by scar tissue

24
Q

What ROP to treat

A

Zone 1 , any ROP with plus disease

zone 1, stage 3 without plus disease

zone 2 stage 3 with plus disease

Consider treateing zone II stage 2 with plus disease

25
What is treatment of ROP
Transpupillary diode laser to give near confluent (0.5-1 burn width) laser burn spacing to the entire avascular retina
26
What is follow up post treatment?
5-7d post treatment Then weekly looking for signs of reduced activity and regression If failure to regress after 10-14d - retreatment
27
What condition do patients have avascular temporal retina?
Familial exudative vitreoretinoapthy FEVR Abrupt cessation of peripheral retinal vessels at the equator and vitreous bands in the periphery leading to retinal ischaemia, fibrovascular proliferation, reitnal folds, RD, subretinal exudation AD (Chr11q) XR (NDP)
28
What is Coar's disease?
Telangiectasia Men, young But can rpesen in adults (asymptomatic til 30s) Unilateral
29
CF of Coats
Asymptomatic Reduced vA Strabismus Lecuocoria Telangiectatic vessels, light bulb aneurysms, capillary dropout, exudation, scarring Complciations: ERD, VH, rubeosis, glaucoma, cataract
30
What does FFA show in Coat's
Abnormal vessels, leakage, capillary dropout
31
What is first line treatment for Coat's
Control exudation - laser photocoagulation or cryo of leaking vessels - treat directly Consider anti-VEGF if exudation prevents laser If exudative RD - Scleral buckle with drainage of SRF
32
What is MacTel type 1
UNILATERAL retinal vascular anomaly CONGENITAL Aneurysmal dilation of retinal vasculature Confined to irregular or oval zone in temporal macula Surrounding CMO Tellowish exudates Microaneurysms TReated with direct laser photocoagulation of aneurysms to decrease exudation and improve VA
33
What is MacTel type 2
ACQUIRED BILATERAL Middle aged/older patients Reduced VA, paracentral scotomas Loss of central macular pigment
34
What is seen on FAF MacTel type 2
Loss of hypofluorescent foveal centre due to loss of central macular pigment
35
Treatment for DMO according to NICE TA274
IVI ranubizumab Central retinal thickness of 400 micrometres or more at the start of treatment The manufacturers of ranibizumab (branded or biosimilar) provide it at a discount level no lower than the discount agreed in the patient access scheme. RISE and RIDE studies - ranubizumab patients required less macular laser