GLAUCOMA 4 - VF Progression and Newer techniques Flashcards

1
Q

what is the main goal of management in glauc px?

A

lowering IOP

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2
Q

list 3 basic ways of controlling glaucoma?

A

DROPS, LASER OR SURGERY- imp to consider in vf progression but also when making clinical trials - eg SLT treatment at moorfields

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3
Q

what are some clinical methods to monitor glauc?

A

-clinical management- px worsening? px stable?
-clinical trials
-benchmark has to be function

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4
Q

what is one limitation of using vf progression as a way to quanitfy glauc?

A

very difficult to detect changes

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5
Q

how can we improve visual field testing?

A
  • explain to px- as results can be confusing
  • supervise
  • environment-quiet+noise free
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6
Q

what is ‘noise’ in relation to vf plots?

A

things that can interfere with the vf plot results

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7
Q

list 6 examples of ‘noise’ (variability)?

A
  1. Pupil size
  2. Refractive error, cataract
  3. Response reliability
  4. Poor fixation
  5. Learning effects
  6. Fatigue effects
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8
Q

is there a gold std method to check for glauc progression?

A

nope

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9
Q

why is it difficult to detect change?

A

Slow process
No natural history-ethically- control needed but that means some ppl wont get tx

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10
Q

typical methods of assessing glauc px?

A
  • optic nerve head
  • oct
  • iops
  • field plots
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11
Q

disadv of vf tests to assess glauc progression? 4 points

A
  • Difficult to do
  • Subjective
  • Not quantitative
  • Based off experience and judgement
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12
Q

what did a study done looking at 5 glauc specialists observing the same vf plots? (interobserver)

A

not 100% agreed with one other- poor interobserver reliability

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13
Q

what are global indices on a vf plot?

A

Mean Defect (MD)- zero means defect is normal for their age, the more negative the worst the VF is
Average of all deviations
Rate of loss (dB/year)

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14
Q

what does a mean defect of zero mean?

A

-means defect normal for age- it is when its negative that the vf is abnormal or worse

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15
Q

disadv of global indices?

A
  • data reduction
    -Poor sensitivity - low number - small md number-might not be sensitive to that tiny change at one or two locations - which might be more important than depression visual field (eg MD: -5db can look different in diff vf plots) md can be stable- and px could still be losing imp vision
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16
Q

what does ‘data reduction mean’?

A

reducing all data down into numbers

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17
Q

what does data reduction lead to?

A

loss of spatial information
i.e. we don’t know WHERE the VF defect is, just that there is one somewhere

18
Q

why might be any reason MD gets worse (besides glauc)?

A

increase in media opacities- eg cataract

19
Q

what is a newer way to measure mean defect at central location

A

visual field index

20
Q

what is a pointwise or point by point method?- detailed diag in lecture

A
  • ANALYSIS done at each location of central field
  • looking at change over time
  • sensitive tests ideal for a clinical trial-picking up small changes
21
Q

what type of software is ‘point by point’ used in?

A

GPA- Glauc progression analysis

22
Q

on a GPA, what does a dot indicate?

A

no change from baseline

23
Q

on a GPA, what does an open triangle indicate?

A

significant change

24
Q

on a GPA what does a black triangle indicate?

A

Change confirmed
- it is a “true change” therefore suspicious
- fallen below baseline on three occasions

25
Q

on a GPA what does half a black triangle indicate?

A

change will be confirmed at next visit

26
Q

how many VFs are needed to detect a ‘true change’?

A

5 VFs!
(baseline is avg of 2 VFs, + 3 follow up visits)

27
Q

on a gpa what does X indicate?

A

‘Too much’ variability
or defect at baseline
(no decision)

28
Q

how many black triangles do you need to be able to say there is likely progression?

A

3!

29
Q

roughly how long after baseline does it take to detect a VF change?

A

2 years (6 month recall and need 5 VFs for a true change to be detected)

30
Q

what is an advantages of GPA and where is it used?

A

very sensitive= used in clinical trials

31
Q

disadvantages of GPA?

A
  • Dependent on Baseline
  • Database?
  • Does not use all the fields
32
Q

Why is it imp to have good software?

A

to help clinical decisions

33
Q

name some vf glaucoma software

A
  • progressor(medisoft)
  • new software- OPEN eyes
  • GPA on Humphrey
34
Q

main things to consider when using vf software for glauc

A

Detecting progression to see if treatment works

Pointwise methods more sensitive

Good software available – Should be used!

35
Q

why is it important to create functional tests or have novel perimetry?

A

Optic nerve will already start damaging itself before symtpoms seen or signs noticed - so structural change before impact on visual function

36
Q

what axons are lost first in glauc and which pathway does this affect

A

Larger axons- first loss to glac- these larger axons belong to magnocellular pathway- can be probed by flickr, colour and emotion

37
Q

what does magnocellular pathway correspond to?

A

High amounts of flicker

Achromatic stimuli

Moving stimuli

Low spatial frequencies

38
Q

as glauc affects magnocellular pathway, what is a proposed method of novel perimetry + state some limitations?

A

-blue on yellow perimetry (SWAP)
-Longer Test! + Adaptation required
-More variability
-Poor response in elderly as yellowing of crystalline lens with age

39
Q

another novel proposed test?

A

frequency doubling test

40
Q

is frequency doubling test more effect at early detection of glauc?

A

No good evidence that the stimuli offers ‘earlier’ detection

But a well-designed instrument- so plus is it takes up less space