Automated threshold perimetry has increasingly become the basis for assessing the adequacy of glaucoma management, yet there are few data suggesting what constitutes normal variation in otherwise well controlled glaucoma, what constitutes a meaningful deviation in a patient with progressive optic nerve damage and how much damage occurs before such differences in the visual field can reliably detected. Automated perimetry generates a wealth of quantitative data, but analytic strategies which might best detect meaningful changes in the visual field have yet to be developed and evaluated. The assessment of progressive visual field loss is of practical importance not only to clinicians in the management of individual patients, but also for evaluating the efficacy of glaucoma treatment in clinical trial settings. This study proposes to develop analytic strategies for assessing progression of visual field loss and to evaluate them against other measures of optic nerve damage. Consecutive automated visual fields of control subjects, patients with ocular hypertensive and glaucoma will be assembled from a variety of sources.The temporal variability of visual field testing will be estimated for each of these groups. Covariates which affect this variability will be used to better distinguish meaningful change from chance variation. Estimates of visual field change will be obtained by regressing several measures of diffuse and localized loss against time and comparing these to other measures of optic nerve damage such as progressive cupping, nerve fiber layer deterioration and changes in manual perimetry. Individual slope estimates will also be improved by adjusting the estimates with data from other subjects at a similar stage of disease.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
1R29EY009130-01A1
Application #
3465872
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1992-01-01
Project End
1996-12-31
Budget Start
1992-01-01
Budget End
1992-12-31
Support Year
1
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Katz, J (2000) A comparison of the pattern- and total deviation-based Glaucoma Change Probability programs. Invest Ophthalmol Vis Sci 41:1012-6
Katz, J; Congdon, N; Friedman, D S (1999) Methodological variations in estimating apparent progressive visual field loss in clinical trials of glaucoma treatment. Arch Ophthalmol 117:1137-42
Katz, J (1999) Scoring systems for measuring progression of visual field loss in clinical trials of glaucoma treatment. Ophthalmology 106:391-5
Lietman, T; Eng, J; Katz, J et al. (1999) Neural networks for visual field analysis: how do they compare with other algorithms? J Glaucoma 8:77-80
Smith, S D; Katz, J; Quigley, H A (1997) Effect of cataract extraction on the results of automated perimetry in glaucoma. Arch Ophthalmol 115:1515-9
Katz, J; Gilbert, D; Quigley, H A et al. (1997) Estimating progression of visual field loss in glaucoma. Ophthalmology 104:1017-25
Smith, S D; Katz, J; Quigley, H A (1996) Analysis of progressive change in automated visual fields in glaucoma. Invest Ophthalmol Vis Sci 37:1419-28
Katz, J; Quigley, H A; Sommer, A (1996) Detection of incident field loss using the glaucoma hemifield test. Ophthalmology 103:657-63
Katz, J; Quigley, H A; Sommer, A (1995) Repeatability of the Glaucoma Hemifield Test in automated perimetry. Invest Ophthalmol Vis Sci 36:1658-64
Katz, J; Tielsch, J M; Quigley, H A et al. (1995) Automated perimetry detects visual field loss before manual Goldmann perimetry. Ophthalmology 102:21-6

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