Lecture 1/2 - Diagnostics Flashcards

1
Q

What is red light/filter used for?

A

travels the furthest - pigmentary disturbances, choroidal ruptures, choroidal nevi, choroidal melanomas

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2
Q

What is blue light/filter used for?

A

NFL, ILM, ERM, retinal folds, cysts

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3
Q

What is green light/filter used for?

A

retinal vasculature, hemorrhages, drusen, exudates

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4
Q

what are the 4 parts to the early phase in FA?

A

choroidal flush, arterial phase, arteriovenous phase, and venous phase

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5
Q

when is the choroidal flush?

A

10-15 seconds after injection, dye in choriocapillaries

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6
Q

when is the arterial phase?

A

1-2 seconds after choroid - about 12 seconds

a delay may indicate injection or circulatory problems = heart or peripheral disease

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7
Q

when is the venous phase?

A

about 30 seconds after injection - maximum vessel filing

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8
Q

what are the 3 main phases of FA?

A

early phase, mid phase (recirculation phase) and late phase

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9
Q

when does the mid phase occur?

A

2-4 minutes - veins and arteries remain roughly equal in brightness

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10
Q

when does the late phase occur?

A

7-15 minutes - gradual elimination of dye from retinal and choroidal vasculature (late staining of optic disc is normal)

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11
Q

what are the 2 main causes of hypofluorescence?

A

vascular filling defect or blockage

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12
Q

if you use a red-free filter to view a dark spot on the retina and it disappears, what was it?

A

choroidal nevus (CHRPE will remain with red-free)

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13
Q

what 2 conditions can cause autofluorescence (or preinjection fluorescence)?

A

optic nerve drusen and optic nerve hemartoma

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14
Q

what causes pseudofluorescence?

A

poorly matched filters

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15
Q

what can cause early hyperflorescence in the retina?

A

abnormal vessels = tortuosity, dilation, anastomosis, neo, aneurysms, telangiectasia, tumor vessels

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16
Q

what can cause early hyperflorescence in the choroid?

A

PE window defect = atrophy or congenital

Abnormal vessels = subretinal neo, inflammation, tumor vessels

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17
Q

what can cause late hyperflorescence in the vitreous?

A

neo, inflammation, tumors

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18
Q

what can cause late hyperflorescence in the retina?

A

cystoid edema or non-cystic edema

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19
Q

what can cause late hyperflorescence in the choroid?

A

pooling or staining

20
Q

what is leakage hyperfluorescence?

A

seepage of NaFl, increases in intensity and margins blur in late phase (Ex: CNVM, DME, Neo)

21
Q

what is staining hyperfluorescence?

A

dye enters tissue and it retains it - intensity increases during transit but then stays the same, margins are distinct (Ex: scar, drusen, optic nerve tissue or sclera)

22
Q

what is pooling hyperfluorescence?

A

accumulation of dye in a fluid-filled space in the retina or choroid, margins are distinct (Ex: RPE detachment in CSR)

23
Q

what is transmission/window defect hyperfluorescence?

A

increased normal choroidal fluorescence through RPE defects or loss of pigment - dye stays in choroid, does not enter retina (Ex: macular hole or RPE loss)

24
Q

how is ICG different than NaFl?

A

higher molecular weight, remains in larger blood vessels (cannot pass through choriocapillaris fenestrations) and is not blocked by melanin/xanthophyll

25
what are the contraindications for ICG?
caution with history of iodine or shellfish allergy and contraindicated in liver disease or DM on Metformin
26
what is OCT used for?
lamellar vs. pseudo/full thickness macular holes, VMT, DME, CSR, AMD
27
what structures in the eye normally autofluoresce?
corneal epithelium/endothelium, lens, macular and RPE pigments
28
why is autofluorescence useful in Bests Disease?
RPE cells are eating up dye and appear hyper (lipofuscin) and RPE cells are dead are hypo
29
what is near infrared reflectance imaging used for?
better resolution of outer retina - RPE, bruch's, and choroidal vessels are more detectable (uses melanin)
30
what is adaptive optics?
uses very high transverse resolution (2um) and capable of visualizing rod photoreceptors
31
what frequency B-scan do we normally use in clinic?
7-10 MHZ (medium) = retina, vitreous, optic nerve
32
when do you use increase gain on a B-scan?
increased tissue penetration and sensitivity but decreased resolution = hemorrhage, syneresis, posterior hyaloid, inflammatory cells
33
when do you use low gain on a B-scan?
good resolution but poor sensitivity = layers or membranes, hyaloid, retina, choroid, retinal break/tear, tumor, macular edema, holes
34
what is an electroretinogram (ERG) and what are the 3 waves?
mass response evoked from the entire retina = A wave is late receptor potential, B wave is on-bipolar potential and C wave is inner retinal potentials
35
when are the inner retinal potentials/C wave (oscillatory potentials) reduced in an ERG?
retinal ischemic states and in some forms of congenital stationary night blindness
36
what do focal and multifocal ERG test?
foveal or parafoveal cones (topographic ERG map of the retina is produced) = plaquenil toxicity
37
what does a bright flash ERG test?
performed pre-op for severely traumatized globes with a brighter than usual stimulus - un-recordable response is a poor prognosis (moderate signal suggests some salvageable retina)
38
what is a pattern ERG?
alternating checkerboard presented to central retina - integrity of optic nerve, ganglion cells and their retinal interactions (early recognition of glaucoma)
39
what conditions have an abnormal ERG?
foveal disease, RP, CRAO
40
what is an elector-oculogram (EOG)?
measures a response from the RPE (+ corneal end and - retinal end)
41
what disease is the EOG severely reduced?
Best disease
42
what is a visually evoked cortical potential (VEP)?
electrical signals generated by occipital visual cortex in response to stimulation of the retina
43
what does the VEP response look like?
2 (N) negative and 2 (P) positive peaks
44
when is VEP used?
assessing misprojection, estimating VA, detecting/localizing VF defects, visual potential, amblyopia/optic neuritis prognosis
45
what is a sub-normal, severely abnormal and nearly extinguished Arden ratio in EOG?
less than 1.86 and less than 1.30