General VF Screening Techniques Flashcards

1
Q

non automated instruments and techniques

A
  • confrontation fields (count to full fingers, field limits confrontations, color confrontations- red cap, face confrontations)
  • tangent screen
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2
Q

sensitivity of confrontations to all types of VF loss:

A

50-60%

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3
Q

sensitivity of confrontations to ON-related VF loss:

A

20-30%

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4
Q

what type of VF loss has a high sensitivity with face confrontations?

A

central scotomas

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5
Q

sensitivity of confrontations to chaismal VF loss

A

40-50%

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6
Q

sensitivity of confrontations to post-chiasmal VF loss

A

> 75%

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7
Q

non-automated strategy that is rapid, informal, very gross, often used, and can check for extinction phenomenon

A

count fingers confrontations

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8
Q

extinction phenomenon can occur in some cases of ____ damage

A

parietal cortex damage

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9
Q

extinction phenomenon presents as what type of loss

A

homonymous hemianopsia contralateral to the lesion

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10
Q

what conditions on count fingers confrontations must be present to see the extinction phenomenon?

A

only if fingers are presented on both sides of the vertical midline simultaneously

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11
Q

non-automated strategy that only tests the absolute limits of the VF, has much variability/fluctuation in peripheral VF, has very limited usefulness

A

field-limits confrontations

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12
Q

why are field-limits confrontations much less useful than count fingers

A

few VF defects affect peripheral VF limits only

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13
Q

what can the red cap test (color confrontations) be useful in detecting?

A

very helpful in detecting mild central or centrocecal scotomas due to optic nerve disease

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14
Q

what can the red cap test (color confrontations) in quadrant comparison specifically be useful in detecting?

A

VF loss from chiasmal compression

  • pituitary adenoma
  • craniopharyngloma
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15
Q

pituitary adenoma would result in what defect on the red cap-quadrant comparison test?

A

superior temporal quadrants ou red cap is less red than superior nasal

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16
Q

craniopharyngloma would result in what defect on the red cap quadrant comparison test?

A

in inferior temporal quandrants OU, red cap is less red than in inferior nasal

17
Q

face confrontations useful in detection of:

A

central scotomas, centrocecal scotomas, altitudinal hemanopsias and metamiorphosia

18
Q

tangent screen technique is useful in diagnosis of:

A

functional vision loss such as hysterical amblyopia

19
Q

SAP automated perimetry

A

standard automated perimetry, white-on-white perimetry

20
Q

3 alternative forms of perimetry list

A
  1. SWAP
  2. FDT
  3. HEP
21
Q

SWAP alternative perimetry is:

A

short wavelength automated, blue stimulus on yellow background perimetry

22
Q

FDT alternative perimetry is:

in FDT and Matrix

A

frequency doubling testing

23
Q

HEP alternative perimetry is:

A

Heidelberg Edge Perimetry, “frequency defined form”

24
Q

2 problems in glaucoma detection with standard white-on-white perimetry (SAP)

A
  1. does not detect glaucomatous change early in many cases
  2. slow, fatiguing causes artifactuous (due to fatigue not disease) VF loss, so reliability and repeatability are often compromised
25
Q

differences in % of ganglion cell loss needed before earliest VF defect for goldman perimetry, automated threshold perimetry, and SWAP or FDT/Matrix

A

Goldman perimetry: 40-50%
Automated threshold perimetry: 30-40%
SWAP, FDT, Matrix: 20-40%

26
Q

3 reasons why standard white-on-white perimetry (SAP) doesn’t detect glaucomatous VF loss early

A
  1. if all ganglion cells are damaged (overlap in receptive fields, mass response)
  2. selective loss theory in glaucoma (certain types of ganglion cells may be damaged before others)
  3. different damage in different eyes (or different types of glaucoma have unique patterns)
27
Q

2 recent strategies to detect glaucomatous field loss earlier

A
  1. reduced redundancy strategy (test only a small % of all ganglion cells)
  2. selective loss strategy (test primarily those ganglion cells that might be selectively damaged in early glaucoma)
28
Q

the 3 ganglion cell pathways

A
  • parvocullar pathway
  • koniocellular pathway
  • magnocellular pathway
29
Q

80% of all retinal ganglion cells are in the ___ pathway

A

P-cell (Parvocellular)

30
Q

ganglion cell pathway that has thinner axons, slower conduction velocity, most responsive to high spatial frequency/ low temporal frequency

A

P parvocellular

31
Q

ganglion cell pathway that has a major role in color vision, spatial resolution, and form vision, and concentrated mostly in central VF

A

P parvocellular

32
Q

15% of all retinal ganglion cells are in the ___ pathway

A

M-cell (Magnoceullar)

33
Q

ganglion cell pathway that has thicker axons, faster conduction velocity, most responsive to low spatial frequencies/high temporal frequencies

A

M magnocellular

34
Q

ganglion cell pathway that has a major role in processing rapid locker and motion, and FDT/Matrix targets

A

M magnocellular

35
Q

K-cell pathway accounts for __% of all RGCs

A

5

36
Q

ganglion cell pathway that has a major role in b-y color opposite processing

A

K koniocellular

37
Q

ganglion cell pathway that can be tested selectively by testing with SWAP

A

K koniocellular