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Selections from the Gullstrand Meeting
May 23-24, 2003, Uppsala, Sweden
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Pamela Sample on Progression
- Subjective judgment of serial visual fields is NOT reproducible
- Two general approaches for judging progressionr Series analyses
- series displays provided by perimeters
- linear regression analysis
- of global indices such as MD or PSD
- point-by-point, such as Progressor
- Single field visit analyzed relative to two reliable baseline
visual fields
- clinical trials scoring methods
- glaucoma change probability
- Currently, no single algorithm for identifying and quantifying progression
in serial visual fields has gained wide acceptance
- Confirmation reduces number of progressed eyes, e.g., EMGT progression:
49%; after first confirmation: 14%; after second confirmation: 8%
- New approaches to assess progression: more sensitive test procedures,
improved perimetric programs, modeling progression, Machine Learning
Classifiers.
- Machine Learning Classifiers:
- are computer-based systems that learn from the data and develop
their own classification algorithms
- can be supervised or unsupervised learning
- can learn complex patterns and trends in the data
- can adapt to create decision surfaces without the constraints
imposed by statistical classifiers
- are unbiased and may identify meaningful patterns that experts
may not see
- Why is it so important to identify progression earlier?
- treatment works; visual function is the ultimate test for success
- prediction of progression not yet possible
- shorter RCTs
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Cristina Leske on Epidemiology:
- in large studies, the prevalence of open-angle glaucoma in persons
40 years and older is:
- -1%-3% in white populations
- ->3%-9% in black populations
- the incidence of glaucoma per year varies between 0.1% and 0.6%
in large studies of persons 40 years and older
- the 4 years incidence in the Barbados study was 0.7% at IOP <= 17
mmHg and 18.3% at IOP > 25 mmHg (25 times higher relative risk)
- high IOP was a major risk factor but (Barbados study):
1/4 OAG developed at IOP <= 13-19 mmHg
1/2 OAG developed at IOP <= 21 mmHg
2/3 OAG developed at IOP <= 25 mmHg
- other risk factors: race, older age, higher IOP, lower perfusion
pressure (blood pressure minus the IOP), family history, myopia; hypertension
and diabetes are associated with higher IOP but not with OAG. future
issues:
- increase of prevalence (aging, global demographic changes
e.g. Asia, Africa)
- strategies to address modifiable and non-modifiable risk factors
- glaucoma screening and natural history
- future research:
- standardized criteria for definitions
- improved diagnostic methods
- incidence and risk factors by race
- gene-environment interactions
- screening methods and effectiveness
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Observations by Anja Tuulonen
- In evidence-based studies 21% of visual fields were not eligible
(mean of four OHT studies, including OHTS), 23% had no disc and retinal
nerve fiber layer photos (mean of seven studies)
- Profound experience is required for judging disc photographs, which
may not be available in general ophthalmological practice
- For confirmation of abnormality or progression, at least three visual
fields (four RCTs) are needed with good reliability, same program, same
instrument.
- In OHTS, disc evaluation doubled the number of progressive cases;
in EMGT, disc evaluation contributed little to overall progression.
Why? (see Heijl in this issue of IGR)
- Absolute risk reduction (ARR) in new progressive cases per year:
treated
untreated
ARR
OHTS
1%
2%
1%
EMGT
8%
10%
2%
The complete text of these three lectures will be available on
a CD-rom to be issued by the Gullstrand organization.
Issue 5-1
Change Issue
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