ArticleTranslational vision science & technology2022
Long- and Short-Term Variability of Perimetry in Glaucoma.
Article in Translational vision science & technology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 13 citations in OpenAlex.
- Eye-tracking biomarkers for glaucoma based on saccadic reaction time: a controlled clinical study.Frontiers in ophthalmology · 2025Trial
- Comparison of AIZE-EX and SITA-standard visual field measurements in patients with glaucoma.Japanese journal of ophthalmology · 2026Article
- Predicting Variability and Reliability in Visual Field Testing: Short- and Long-Term Approaches.Ophthalmology science · 2026Article
- Evaluation of the visual field test algorithm: the Ambient Interactive ZEST-EX (AIZE-EX).Scientific reports · 2026Article
- ET-1, MMPs, ZAG, and APN Link Reduced Ocular Perfusion to Glaucoma.Biomolecules · 2025Article
- High-density perimetry in the assessment of foveal avascular zone and macular structure in glaucoma.PloS one · 2025Article
- Improving the Accuracy and Speed of Visual Field Testing in Glaucoma With Structural Information and Deep Learning.Translational vision science & technology · 2023Article
- Detectability of Visual Field Defects in Glaucoma Using Moving Versus Static Stimuli for Perimetry.Translational vision science & technology · 2023Article
- A Data-Driven Model for Simulating Longitudinal Visual Field Tests in Glaucoma.Translational vision science & technology · 2023Article
Corrections and comments
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
Abstract
Purpose: Test-retest variability in perimetry consists of short-term and long-term components, both of which impede assessment of progression. By minimizing and quantifying the algorithm-dependent short-term variability, we can quantify the algorithm-independent long-term variability that reflects true fluctuations in sensitivity between visits. We do this at locations with sensitivity both < 28 dB (when the stimulus is smaller than Ricco's area and complete spatial summation can be assumed) and > 28 dB (when partial summation occurs). Methods: Frequency-of-seeing curves were measured at four locations of 35 participants with glaucoma. The standard deviation of cumulative Gaussian fits to those curves was modeled for a given sensitivity and used to simulate the expected short-term variability of a 30-presentation algorithm. A separate group of 137 participants was tested twice with that algorithm, 6 months apart. Long-term variance at different sensitivities was calculated as the LOESS fit of observed test-retest variance minus the LOESS fit of simulated short-term variance. Results: Below 28 dB, short-term variability increased approximately linearly with increasing loss. Long-term variability also increased with damage below this point, attaining a maximum standard deviation of 2.4 dB at sensitivity 21 dB, before decreasing due to the floor effect of the algorithm. Above 30 dB, the observed test-retest variance was slightly smaller than the simulated short-term variance. Conclusions: Long-term and short-term variability both increase with damage for perimetric stimuli smaller than Ricco's area. Above 28 dB, long-term variability constitutes a negligible proportion of test-retest variability. Translational Relevance: Fluctuations in true sensitivity increase in glaucoma, even after accounting for increased short-term variability. This long-term variability cannot be reduced by altering testing algorithms alone.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.