D - Visual Field Assessment in Glaucoma - Week 1 Flashcards

1
Q

Why is visual field assessment essential for glaucoma? (4)

A

disease detection
disease monitoring
assessing impact on tasks of daily living
fitness to drive

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2
Q

In VF testing, what should the false positive rate be less than for the test to be reliable?

A

20%

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3
Q

What could be one potential reason for high fixation losses in an otherwise normal patient? (i.e. not malingering, no motility problems, etc.)

A

Blindspot in unique position. Test/machine assumes blindspot in average position, resulting in apparent fixation losses

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4
Q

What is total deviation? What is it good for?

A

the dB value you are away from age-matched normals (e.g. +5dB = 5dB better than normals)

good to see if outside normal limits (i.e. 95% CI)

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5
Q

What do pattern deviation maps look for?

A

looks for deviations from your own hill of vision

(e.g. if you are worse than others in sensitivity, that generalised difference gets subtracted out so you can focus specifically on changes to your own hill of vision)

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6
Q

What is Mean deviation (MD) in perimetry?

A

MD measures the mean defect across the visual field (i.e. the average of deviations in all test locations across the visual field)

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7
Q

Why would you perform macula testing (10-2) on a glaucoma patient? What is the advantage of a 10-2 over a 24-2?

A

Macula testing gives you refined detail of defects in central vision compared to the standard 24-2 or 30-2. When 24-2 picks up one deviated spot in the central 10 degrees, macula testing can identify if the region of defect in greater detail.

Because 24-2 only tests vision every 6 degrees apart whereas 10-2 tests vision every 2 degrees apart.

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8
Q

What is the main disadvantage of a 10-2?

A

Doubles testing duration compared to 24-2. This is why we only use it when indicated (i.e. when we see a bit of central defect/loss - even if just one spot)

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9
Q

Which perimeter device is better at picking up central defects: Humphrey or Medmont?

A

Medmont has more locations tested in the fovea so will pick up more central defects by default

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10
Q

What type of instruction should you give to patients for visual field testing for the best results? Liberal, Neutral, or Conservative

A

Realistically it’s fine as long as everyone uses the same instructions. Ideally you’d want neutral instructions however.

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11
Q

Give an example of good visual field instruction

A

“Some lights will be dim, some brighter. We are trying to measure how dim the lights can be for you to just be able to see them. Maintain fixation on the central light. When you see a light, press the button. We also want to know when you can’t see the light, so don’t panic if you don’t see anything”

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12
Q

How can the false +ve/false -ve rate be described graphically?

A

As a psychometric function of probability

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13
Q

What does a flat psychometric false+ve/false-ve function for perimetry suggest?

A

that there is a genuine probability that a light you saw before won’t be seen next time and vice-versa

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14
Q

True or False: Psychometric function for seeing or not seeing a stimulus changes across the visual field

A

true

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15
Q

Are visual field results in locations with high confidence intervals reliable for measuring progression of loss or defect?

A

No

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16
Q

What is the main thing you should check for in the visual field of a glaucoma suspect?

A

Visual field asymmetry + patterns that can be explained by RNFL defect

17
Q

Why can’t you numerically compare HFA vs Medmont results? (3)

A

They arrange spots in different areas of space (Humphrey = grid, Medmont = ring) and the dB scales + maths is different. And also the max brightness differs too.

18
Q

What is event analysis?

A

little symbols to indicate progression and show whether it’s been reported consecutively

19
Q

What do global indices show you?

A

shows how the whole visual field is changing

20
Q

What does trend analysis project?

A

projects expected change over time based on previous/current data

21
Q

Give one reason why SITA-faster is faster?

A

it doesn’t check the blindspot location

22
Q

List the criteria used to identify an early glaucomatous defect (stage 1)

A

MD >/= -6.00 dB and one of the following:
A: Pattern deviation - cluster of 3 or more points in an expected location of the VF depressed below 5% level, at last 1 of which is depressed below the 1% level
B: Corrected pattern stdv./pattern stdv. significant at P<0.05
C: Glaucoma hemifield test “Outside Normal Limits”

23
Q

List the criteria used to identify an moderate glaucomatous defect (stage 2)

A

MD -6.01 to -12.00dB and one of the following:
A: Pattern deviation - >/= to 25% but <50% of pts depressed below 5% level, and 15-<25% depressed below 1% level
B: At least 1 pt. within central 5deg with sensitivity <15dB but, no point within central 5deg with sensitivity <0dB
C: Only 1 hemifield containing a pt. with sensitivity <15dB within 5deg of fixation

24
Q

List the criteria used to identify an advanced glaucomatous defect (stage 3)

A

MD -12.01 to -20.00dB and one of the following:
A: Pattern deviation - 50-<75% of pts depressed below 5% level, and 25-<50% depressed below 1% level
B: Any pt. within central 5deg with sensitivity <0dB
C: Both hemifields containing a pt. with sensitivity <15dB within 5deg of fixation

25
Q

List the criteria used to identify a severe glaucomatous defect (stage 4)

A

MD -20.00dB and one of the following:
A: Pattern deviation - >/=75% of pts depressed below 5% level, and >/=50% depressed below 1% level
B: At least 50% of pts. within central 5deg with sensitivity <0dB
C: Both hemifields containing >50% of pts. with sensitivity <15dB within 5deg of fixation

26
Q

List the criteria used to identify a end stage glaucoma (stage 5)

A

Unable to perform Humphrey visual fields in “worst eye” attributable to central scotoma or “worst eye” visual acuity of 20/200 or worse attributable to POAG. “Best eye” may be at any stage