Abstract:To evaluate the utility of a computer controlled two-bar Vernier acuity measurement as a predictor of visual function in the presence of cataract we measured logMAR visual acuity and Vernier acuity in a group of 40 young normal observers under various levels of dioptric blur (0-3 D in dioptre steps). The Vernier thresholds were resistant to dioptric blur up to 2 D, but performance degraded with blur of 3 D for non-optimised Vernier stimulus parameters. The stimulus parameters, bar length and bar separation, we… Show more
“…Myopic defocus (+1.00 DS) degraded distance HCVA by ~30% less than astigmatism, close to the power strength ratio (0.71) prediction . The spherical blur was less than that found in phakic eyes, possibly related to the extended depth‐of‐focus interval in pseudophakic eyes . For near vision, spherical refraction changes near VA by ~0.18 logMAR/DS compared with the ~0.10 logMAR/DC provided by the astigmatic refraction.The present data suggests that a pseudophakic eye with 1.00 DS of myopia will have better distance and approximately the same near VA as an astigmatic eye with 2.00 DC.…”
Simple myopic astigmatism improved near visual performance in pseudophakic eyes at the expense of some deterioration in distance performance. ATR astigmatism degraded VA at distance marginally more than WTR astigmatism and provided a marginally better VA at near. However, the benefit at near was more explicit when measured by reading performance, confirming the role of blur orientation on visual performance.
“…Myopic defocus (+1.00 DS) degraded distance HCVA by ~30% less than astigmatism, close to the power strength ratio (0.71) prediction . The spherical blur was less than that found in phakic eyes, possibly related to the extended depth‐of‐focus interval in pseudophakic eyes . For near vision, spherical refraction changes near VA by ~0.18 logMAR/DS compared with the ~0.10 logMAR/DC provided by the astigmatic refraction.The present data suggests that a pseudophakic eye with 1.00 DS of myopia will have better distance and approximately the same near VA as an astigmatic eye with 2.00 DC.…”
Simple myopic astigmatism improved near visual performance in pseudophakic eyes at the expense of some deterioration in distance performance. ATR astigmatism degraded VA at distance marginally more than WTR astigmatism and provided a marginally better VA at near. However, the benefit at near was more explicit when measured by reading performance, confirming the role of blur orientation on visual performance.
“…Quaid et al ( 2002 ) reported a correlation coefficient between Vernier acuity and optotype acuity of r = 0.8 for normal subjects. In our total population, we find that r = 0.52 ( p < 0.001); for our controls, we find r = 0.55 ( p = 0.0025); and for ASD, we find r = 0.57 ( p = 0.0057).…”
A common neurodevelopmental disorder, autism spectrum disorder (ASD), is defined by specific patterns in social perception, social competence, communication, highly circumscribed interests, and a strong subjective need for behavioral routines. Furthermore, distinctive features of visual perception, such as markedly reduced eye contact and a tendency to focus more on small, visual items than on holistic perception, have long been recognized as typical ASD characteristics. Recent debate in the scientific community discusses whether the physiology of low-level visual perception might explain such higher visual abnormalities. While reports of this enhanced, “eagle-like” visual acuity contained methodological errors and could not be substantiated, several authors have reported alterations in even earlier stages of visual processing, such as contrast perception and motion perception at the occipital cortex level. Therefore, in this project, we have investigated the electrophysiology of very early visual processing by analyzing the pattern electroretinogram-based contrast gain, the background noise amplitude, and the psychophysical visual acuities of participants with high-functioning ASD and controls with equal education. Based on earlier findings, we hypothesized that alterations in early vision would be present in ASD participants. This study included 33 individuals with ASD (11 female) and 33 control individuals (12 female). The groups were matched in terms of age, gender, and education level. We found no evidence of altered electrophysiological retinal contrast processing or psychophysical measured visual acuities. There appears to be no evidence for abnormalities in retinal visual processing in ASD patients, at least with respect to contrast detection.
“…22 The effects of contrast reduction are greater on stereoacuity than on Vernier acuity. 20 Thus the differences we found between the stereoblind and stereoscopic subgroups could result from some optical degradation (perhaps refractive error, cataract, and/or deposits in the cornea) which was large enough to produce a differential effect on Landolt acuity and stereoacuity, but not large enough to affect Vernier acuity differentially. This notion is also supported by the correlation between Landolt acuity and stereoacuity in the stereoscopic patient subgroup.…”
Section: Correlationsmentioning
confidence: 74%
“…In contrast, our data from the Landolt test, showing greater impairment in the stereoblind subgroup, appear to be consistent with differences within the eyeball, either optical or retinal, between the two patient subgroups. For example, Quaid et al 20 showed that blurring with positive lenses or with contact lenses which simulate cataracts had a greater effect on letter than on Vernier acuity. In their study, blurring had little effect on Vernier acuity below two dioptres.…”
We investigated an effect of end-stage renal disease (ESRD) on the visual system by measuring the ability of 21 patients to perceive depth in the random dot stereograms and circles of the Randot Test. To control for other factors which might influence performance on the tests of stereopsis, patients were compared with healthy controls matched for age, years of education, IQ, and general cognitive ability. Vernier acuity (thought to reflect mainly central processing) and Landolt acuity (more sensitive to retinal and optical abnormalities) were also measured, but the study did not include a formal ophthalmological examination. All controls could perceive depth in random dot stereograms, whereas 9/21 patients could not. Patients who could perceive depth had worse stereoacuity than did their matched controls. The patient group as a whole had worse Vernier and Landolt acuities than the controls. The stereoblind patient subgroup had similar Vernier acuity to the stereoscopic subgroup, but worse Landolt acuity, and was more likely to have peripheral vascular disease. We conclude that ESRD had affected structures both within the eye, and within the visual brain. However, the similarity of Vernier acuity and difference of Landolt acuity in the stereoblind and stereoscopic patient subgroups suggest that the differences in stereoscopic ability arise from abnormalities in the eyes rather than in the brain.
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