- •Preface
- •Analysis of field data
- •Interpolation of perimetric test grids using artificial neural networks
- •A new scoring program for quantification of the binocular visual field
- •A variance-equalizing transformation for the analysis of visual fields
- •Mixture of factor analysis of standard visual fields
- •Variability components of standard perimetry
- •Comparison of different methods for detecting glaucomatous visual field progression
- •Clinical perimetry
- •Does patient education result in more reliable initial visual fields?
- •Tendency oriented perimetry in children with ocular abnormalities
- •A computer application for training kinetic perimetry
- •Evaluation of stato-kinetic dissociation using examiner-independent automated perimetric techniques
- •Prevalence and characteristics of central binocular visual field defects in patients attending a glaucoma perimetry service
- •Comparison of tests
- •Comparison of conventional automated perimetry, short-wavelength automated perimetry and frequency-doubling technology in the assessment of patients with multiple sclerosis
- •Conventional perimetry and frequency-doubling technique
- •Tendency oriented perimetry versus Fastpac in patients with neuro-ophthalmological defects
- •Comparison of selected parameters of SITA Fast and Full Threshold strategies in evaluation of glaucoma suspects
- •Continuous light increment perimetry (CLIP) strategy compared to full threshold strategy in glaucoma patients
- •Frequency-doubling technology and high-pass resolution perimetry in glaucoma and ocular hypertension
- •Glaucoma
- •Glaucoma diagnosis using tendency oriented perimetry
- •Influence of optic disc appearance and diurnal variation of intraocular pressure on visual field defect in normal tension glaucoma
- •The relationship between perimetric and metabolic defects caused by experimental glaucoma
- •Combining structural and functional assessment to detect glaucoma
- •New perimetric techniques
- •Utility of a dynamic termination criterion in bayesian adaptive threshold procedures
- •Novel 3D computerized threshold Amsler grid test
- •Second generation of the tendency oriented perimetry algorithm in glaucoma patients
- •SITA-standard and short-wavelength automated perimetry in the early diagnosis of glaucoma
- •Realization of semi-automated kinetic perimetry with the Interzeag Octopus 101 instrument
- •Resolution perimetry using Landolt C
- •Combined spatial, contrast and temporal function perimetry in early glaucoma and ocular hypertension
- •Objective measures
- •Detection of glaucomatous visual field loss using multifocal visual evoked potential
- •The multifocal visual evoked potential in functional visual loss
- •Multifocal visual evoked potential in optic neuropathies and homonymous hemianopias
- •Optic nerve head imaging
- •Confirmatory results in suspect glaucoma patients with normal visual field and abnormal retinal nerve fiber layer findings
- •Discriminating analysis formulas for detecting glaucomatous optic discs
- •Reproducibility of the Heidelberg Retina Flowmeter by automatic full field perfusion image analysis
- •The ability of the Heidelberg Retina Tomograph and GDx to detect patients with early glaucoma
- •Assessment of digital stereoscopic optic disc images using a Z Screen
- •The correlation between change in optic disc neuroretinal rim area and differential light sensitivity
- •The effect of contour-line drawing criteria on optic disc parameters as measured with the Heidelberg Retina Tomograph
- •Evaluation of effectiveness of new GDx parameters
- •Psychophysics
- •Spatial summation for single line and multi-line motion stimuli
- •Normal relationship between luminous threshold and critical flicker fusion frequency
- •Perimetric measurement of contrast sensitivity functions
- •Association between birth weight deviation and visual function
- •Retinal and neurological disorders
- •Natural course of homonymous visual field defects as a function of lesion location, pathogenesis and scotoma extent
- •A relative afferent pupillary defect is an early sign of optic nerve damage in glaucoma
- •Visual field changes after pars plana vitrectomy and internal limiting membrane peeling
- •The relationship between retinal contraction and metamorphopsia scores in patients with epiretinal membranes
- •Screening
- •Frequency-doubling technology staging system accuracy in classifying glaucomatous damage severity
- •A new screening program for flicker perimetry
- •Screening for glaucoma in a general population with a non-mydriatic fundus camera and a frequency-doubling perimeter
- •Index of Authors
Mixture of factor analysis of standard visual fields |
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MIXTURE OF FACTOR ANALYSIS OF STANDARD VISUAL FIELDS
PAMELA A. SAMPLE,1 KWOKLEUNG CHANG,3 CATHERINE BODEN,1 TE-WON LEE,3 ROBERT N. WEINREB,1 TERRENCE SEJNOWSKI2 and MICHAEL H. GOLDBAUM1
1Glaucoma Center, Department of Ophthalmology, University of California at San Diego; 2Computational Neurobiology Laboratory, Salk Institute; 3Institute for Neural Computation, University of California at San Diego; La Jolla, CA, USA
Abstract
Purpose
To extract patterns of field loss using variational bayesian mixture of factor analysis (vbMFA).
Methods
Standard perimetry absolute threshold values for 52 locations plus age from one eye each of 156 patients diagnosed with glaucomatous optic neuropathy (GON) and 189 normals were evaluated with unsupervised vbMFA to separate the fields into clusters. Fields were not used to select subjects.
Results
The vbMFA formed four distinct clusters. The ‘normal cluster’ held 186 normals + 45 patients. Each GON cluster could be represented by a ‘typical’ pattern of defect: GON1 (56 patients + 3 normals) by a general reduction with MD of –2.65 ± 1.72; GON 2 (39 patients) by a superior hemifield defect, and GON 3 (16 patients) by an inferior hemifield defect with or without superior field involvement. Specificity was 98%; sensitivity was 71%.
Conclusions
vbMFA accurately clustered patients into groups with typical glaucomatous patterns of loss. vbMFA may be very helpful for learning patterns of defect in newer psychophysical tests that have different numbers and locations for test stimuli.
Acknowledgment
Supported by NIH Grants EY08208 (PAS), EY13235 (MHG), Research to Prevent Blindness (PAS), Howard Hughes Medical Institute (TS). Commercial relationships: none.
Address for correspondence: Pamela A. Sample, PhD, Department of Ophthalmology, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0946, USA. Email: psample@eyecenter. ucsd.edu
Perimetry Update 2002/2003, p. 35
Proceedings of the XVth International Perimetric Society Meeting, Stratford-upon-Avon, England, June 26–29, 2002
edited by David B. Henson and Michael Wall
© 2004 Kugler Publications, The Hague, The Netherlands
Variability components of standard perimetry |
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VARIABILITY COMPONENTS OF STANDARD PERIMETRY
PAUL G.D. SPRY1,2 and CHRIS A. JOHNSON1
1Discoveries in Sight, Portland, OR, USA; 2Bristol Eye Hospital, Bristol, UK
Abstract
Background
Responsiveness to light stimuli at a single test location varies according to a psychometric function, the frequency-of-seeing curve. This function can be used to precisely define threshold (50% detection level) and response variability (slope). Although the relationship between threshold sensitivity and response variability in glaucoma has been described by a number of investigators, 1-3 the temporal behavior of other frequency-of-seeing curve parameters, or variability components, remain uncharacterized. Specifically, it is possible that the frequency-of-seeing curve gradient from a particular test location may not remain constant and could change in shape over relatively short time periods. Furthermore, it is also possible that the curve may retain a constant shape but may shift laterally in sensitivity space.
Purpose
To examine the temporal behavior of precisely measured threshold and response variability.
Methods
Eight trained normal individuals and seven glaucoma patients were examined using standard perimetry. The method of constant stimuli was used to test three test locations in a single eye of each subject using an externally controlled Humphrey Field Analyzer I. Subjects were tested once weekly at the same test locations for five consecutive weeks. Frequency-of-seeing curves were constructed by fitting data with cumulative gaussian functions and were used to define threshold (50% detection level, dB) and response variability (frequency-of-seeing curve inter-quartile range, dB). The distribution of both of these parameters (inter-quartile range, dB) over the study period was used to quantify their temporal behavior.
Results
As reported by previous investigators, response variability was found to be higher (shallower frequency- of-seeing curve slope) in glaucoma patients than normal individuals (p < 0.001). Additionally, variations in both threshold sensitivity and response variability were observed and found to be significantly greater in glaucoma patients than normal individuals.
In glaucoma patients, mean (standard deviation) response variability was 6.2 (5.0) dB and was greater than both mean threshold sensitivity variation and mean frequency-of-seeing curve slope variation, which were measured as 2.5 (2.1) dB and 3.3 (3.4) dB, respectively. No significant difference existed between the amount of threshold sensitivity variation and frequency-of-seeing curve slope variation, although both were inversely related to mean threshold sensitivity.
Address for correspondence: Paul G.D. Spry, PhD, Bristol Eye Hospital, Lower Maudlin Street, Bristol, BS1 2LX, UK. Email: paul.spry@ubht.swest.nhs.uk
Perimetry Update 2002/2003, pp. 37–38
Proceedings of the XVth International Perimetric Society Meeting, Stratford-upon-Avon, England, June 26–29, 2002
edited by David B. Henson and Michael Wall
© 2004 Kugler Publications, The Hague, The Netherlands
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P.G.D. Spry and C.A. Johnson |
Changes in threshold sensitivity and response variability for test locations tested within each individual did not occur in parallel for the majority of subjects.
Discussion
In this experiment, three components of threshold measurement variability have been described. The first of these is the slope of the psychometric function (frequency-of-seeing curve). Data obtained in this experiment for this variability component, response variability, are in agreement with that reported by previous investigators, who have shown that the frequency-of-seeing curve becomes shallower with increases in threshold (reductions in sensitivity) that occur in glaucoma.1-3 The other two variability components we have described occur over a longer time period than response variability. These longerterm components consist of change in threshold and change in response variability over time. Both these longer-term variability components appear to increase with threshold in patients with glaucoma, although to a significantly lesser extent than shallowing of the curve slope. No evidence was found to suggest that changes in slope or sensitivity at one test location in any given field were similar to changes occurring at other test locations elsewhere within the same visual field.
References
1.Weber J, Rau S: The properties of perimetric thresholds in normal and glaucomatous eyes. German J Ophthalmol 1: 79-85, 1992
2.Chauhan BC, Tompkins JD, LeBlanc RP, McCormick TA: Characteristics of frequency-of-seeing curves in normal subjects, patients with suspected glaucoma, and patients with glaucoma. Invest Ophthalmol Vis Sci 34:3534-3540, 1993
3.Henson DB, Chaudry S, Artes PH, Faragher EB, Ansons A: Response variability in the visual field: comparison of optic neuritis, glaucoma, ocular hypertension, and normal eyes. Invest Ophthalmol Vis Sci 41:417-421, 2000
