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Comparisons of Two Microperimeters: The Clinical Value of an Extended Stimulus Range
Arango, Tiffany; Morse, Alan R; Seiple, William
SIGNIFICANCE/CONCLUSIONS:Fundus-guided perimetry is a common clinical tool used to measure visual field sensitivities. Comparisons between perimeters are often made despite relative differences in hardware parameters. We directly compared two perimeters using Weber contrast, which allowed us to assess the clinical gain associated with the extended stimulus range of the macular integrity assessment (MAIA). PURPOSE/OBJECTIVE:The purpose of this study was to directly compare sensitivity thresholds for two microperimeters, the MAIA and Optos optical coherence tomography/scanning laser ophthalmoscope, using Weber contrast values. We also examined the clinical utility of the extended stimulus range of the MAIA. METHODS:Six normally sighted adults with no visual field loss and 16 adults with low vision were recruited. Thresholds were measured on the MAIA and Optos using the same threshold algorithm and test points. To compare equivalent units, decibel thresholds were converted to light increments in apostilbs and then to delta increment intensities relative to each instrument's background luminance. Repeatability was assessed for normally sighted adults by testing both instruments on 3 separate days. RESULTS:For normally sighted observers, mean thresholds were similar on both instruments, and repeatability within microperimeters was high. The MAIA has a 0.3-log lower contrast range and 1.37 higher contrast range. The lower contrast values did not result in lower thresholds for the normally sighted observers on the MAIA. There was a 25% increase in the number of measurable thresholds owing to the higher contrast values in low-vision observers. CONCLUSIONS:The higher contrast range in the MAIA yielded only a small increase in detectable thresholds for participants with visual field loss.
PMID: 30063665
ISSN: 1538-9235
CID: 3217392
Effects of Lighting on Reading Speed as a Function of Letter Size
Seiple, William; Overbury, Olga; Rosenthal, Bruce; Arango, Tiffany; Odom, J Vernon; Morse, Alan R
OBJECTIVE:We sought to determine under what conditions brighter lighting improves reading performance. METHOD:Thirteen participants with typical sight and 9 participants with age-related macular degeneration (AMD) read sentences ranging from 0.0 to 1.3 logMAR under luminance levels ranging from 3.5 to 696 cd/m². RESULTS:At the dimmest luminance level (3.5 cd/m²), reading speeds were slowest at the smaller letter sizes and reached an asymptote for larger sizes. When luminance was increased to 30 cd/m², reading speed increased only for the smaller letter sizes. Additional lighting did not increase reading speeds for any letter size. Similar size-related effects of luminance were observed in participants with AMD. CONCLUSION:In some instances, performance on acuity-limited tasks might be improved by brighter lighting. However, brighter lighting does not always improve reading; the magnitude of the effect depends on the text size and the relative changes in light level.
PMCID:5807403
PMID: 29426392
ISSN: 0272-9490
CID: 3036632
Stargardt Macular Dystrophy: Changes in Fixation When Asked to Look Straight Ahead
Jackson, Mary Lou; Seiple, William
PURPOSE/OBJECTIVE:To examine whether individuals with Stargardt disease macular dystrophy (STGD) change the location of fixation with instruction. DESIGN/METHODS:Case-control study. PARTICIPANTS/METHODS:Thirteen normally sighted and 37 STGD participants. METHODS:Using an Optos scanning laser ophthalmoscopy/OCT microperimeter (Optos plc, Dunfermline, UK), fixation was measured under 2 different instructions: "look at the cross" (LC) and "look straight ahead, even if you do not see the cross" (LS). Visual acuity, contrast sensitivity, disease duration, and age at disease onset were obtained from medical records. MAIN OUTCOME MEASURE/METHODS:Change in fixation with instruction. RESULTS:Mean age of the STGD participants was 39.2 years, and 24 were women. Mean acuity was 1.01±0.29 logarithm of the minimum angle of resolution (logMAR), and mean contrast sensitivity was 1.16±0.41 log. The largest number of fixations under the LC condition were in the superior retina. Patients with STGD were divided into 3 groups, depending on the change in fixation locus when asked to look straight ahead: those having fixation closer the fovea, those with no change in the location of fixation, and those looking farther away from the fovea. Fifty-one eyes of 32 participants had fixations closer to the fovea when asked to look straight ahead (average change, -6.3°), whereas 13 eyes of 11 participants did not change fixation. There were no significant differences between groups in age, visual acuity, contrast sensitivity, bivariate contour ellipse area, and age at disease onset. CONCLUSIONS:Despite having eccentric fixation, most STGD participants did not have a complete directional re-referencing from the fovea to the eccentric location, and moved fixation when asked to look straight ahead. This finding emphasizes that reliable assessment of visual function during evaluations of disease progression or in therapeutic intervention trials requires consistent instructions and monitoring of fixation. Otherwise, a patient's interpretation of fixation instruction may confound the results.
PMID: 31047447
ISSN: 2468-7219
CID: 3834732
Comparisons of MAIA and Optos Microperimeters [Meeting Abstract]
Arango, Tiffany; Seiple, William H; Maeng, Meesa; Szlyk, Janet P
ISI:000394210600088
ISSN: 0146-0404
CID: 2492242
Light, What Is It Good For? [Meeting Abstract]
Seiple, William H; Overbury, Olga; Odom, JVernon; Arango, Tiffany; Morse, Alan R
ISI:000394174004267
ISSN: 0146-0404
CID: 2507112
Validating a self-guided reading-eye-movement training program [Meeting Abstract]
Maeng, M; Seiple, W H; Kilbride, P; Jackson, C; Szlyk, J P
Purpose: Previous research has demonstrated that oculomotor control training results in increased reading speed in patients with central scotomas due to retinal disease. Typically, reading-eye-movement training takes place in clinical settings and is executed by a therapist who provides guidance and immediate performance feedback. In-home vision rehabilitation has the potential to reduce travel, and expenses for patients and allow more frequent training. This study validated the effectiveness of an interactive, self-guided eye movement training program that could be independently used in the home. Methods: Eight subjects with central scotomas due to retinal disease participated in the 8-week study. The median age of subjects was 51 years (range, 25-94 years). Binocular visual acuity ranged from 20/80 to 20/400, and contrast sensitivity ranged from 0.56-1.88 log CS. Subjects performed eye movement training tasks once per week for one hour on a user-friendly computer platform, developed using methods from our previous research. The interface is fully accessible, consisting of large icons, touch-screen displays, speech recognition, and voice controls. The platform allows participants to self-administer training exercises by automatically selecting appropriate modules based on past training performance, executing the training exercise, and storing training data. The binocular training program advances from single- to three-letter word saccades and progressed from small saccades to larger eye movements. All subjects were trained to navigate the program and were required to demonstrate proficiency before beginning independent training. Outcome measures (MNREAD, visual acuity, contrast sensitivity, microperimetry thresholds) were assessed at baseline, 1 month, and post-training. Results: Mean reading speed at baseline was 69.3 wpm. Reading speed increased by an average of 44.2 wpm (63.7%) after 8 weeks of self-guided eye-movement training. Improvement in reading speed was independent of age, acuity, contrast sensitivity, and reading speed at baseline (p<.05). Conclusions: Consistent with our previous work, a computer platform designed for independent training of eye-movement control increased reading speed in subjects with central scotomas due to retinal disease. Our findings suggest that the platform could be effectively used for automated, in-home training
EMBASE:616039328
ISSN: 0146-0404
CID: 2565152
Ophthalmologic Baseline Characteristics and 2-Year Ophthalmologic Safety Profile of Pramipexole IR Compared with Ropinirole IR in Patients with Early Parkinson's Disease
Seiple, William; Jennings, Danna; Rosen, Richard B; Borchert, Leona; Canale, Lee; Fagan, Nora; Gordon, Mark Forrest
Background. Parkinson's disease (PD) progressively affects dopaminergic neurotransmission and may affect retinal dopaminergic functions and structures. Objective. This 2-year randomized, open-label, parallel-group, flexible-dose study, NCT00144300, evaluated ophthalmologic safety profiles of immediate-release (IR) pramipexole and ropinirole in patients with early idiopathic PD with =6 months' prior dopamine agonist exposure and without preexisting major eye disorders. Methods. Patients received labeled IR regimens of pramipexole (n = 121) or ropinirole (n = 125) for 2 years. Comprehensive ophthalmologic assessments (COA) included corrected acuity, Roth 28-color test, slit-lamp biomicroscopy, intraocular pressure, computerized visual field test, fundus photography, and electroretinography. Results. At baseline, we observed retinal pigmentary epithelium (RPE) hypopigmentation not previously reported in PD patients. The estimated relative risk of 2-year COA worsening with pramipexole versus ropinirole was 1.07 (95% CI: 0.71-1.60). Mean changes from baseline in Unified Parkinson's Disease Rating System parts II+III total scores (pramipexole: 1 year, -4.1 +/- 8.9, and 2 years, -0.7 +/- 10.1, and ropinirole: 1 year, -3.7 +/- 8.2, and 2 years, -1.7 +/- 10.5) and Hoehn-Yahr stage distribution showed therapeutic effects on PD symptoms. Safety profiles were consistent with labeling. Conclusions. The risk of retinal deterioration did not differ in early idiopathic PD patients receiving pramipexole versus ropinirole. RPE hypopigmentation at baseline was not previously reported in this population. This trial is registered with NCT00144300.
PMCID:5203898
PMID: 28078162
ISSN: 2090-8083
CID: 2400812
The Functional Performance of the BrainPort V100 Device in Persons Who Are Profoundly Blind
Grant, Patricia; Spencer, Lindsey; Arnoldussen, Aimee; Hogle, Rich; Nau, Amy; Szlyk, Janet; Nussdorf, Jonathan; Fletcher, Donald C; Gordon, Keith; Seiple, William
Structured abstract: Introduction: This study was conducted to evaluate the functional performance of the BrainPort V100 device, an FDA-cleared sensory-substitution system, in persons who are profoundly blind (that is, have some or no light perception). Methods: This was a prospective, single-arm, multicenter clinical investigation. Participants received 10 hours of device training and were required to use the device in their everyday environments for 1 year. Functional performance measures of object identification, orientation and mobility (O&M), and word identification were assessed at baseline, in post-device training, and at the 3-, 6-, 9-, and 12-month time points. Results: Fifty-seven participants completed the study and used the device for 1 year. No device-related serious adverse events were reported, demonstrating that the risks associated with the BrainPort are minimal. Participants performed object recognition (91.2% success rate) and O&M (57.9% success rate) tasks beyond chance level. Discussion: This study demonstrates that the BrainPort can be used safely and independently by persons who are blind. Participants with profound blindness can accomplish a set of tasks more successfully by using the BrainPort than without the device. Following initial training, performance on these tasks was maintained or improved over the course of 1 year. Implications for practitioners: The BrainPort is a noninvasive and nonsurgical device that heightens functional independence for persons who are blind. The device presents users with more information about their environment than conventional assistive devices, and can enhance independence in performing activities of daily living.
ISI:000372147900001
ISSN: 1559-1476
CID: 2064622
Do patients with Stargardt maculopathy fixate eccentrically or with their fovea when asked to look straight ahead? [Meeting Abstract]
Jackson, Mary Lou; Selivanova, Alexandra; Seiple, William
ISI:000362882201304
ISSN: 0146-0404
CID: 1830442
Abnormal fixation in individuals with age-related macular degeneration when viewing an image of a face
Seiple, William; Rosen, Richard B; Garcia, Patricia M T
PURPOSE: It has been reported that patients with macular disease have difficulties with face perception. Some of this difficulty may be caused by the sensory and perceptual consequences of using peripheral retina. However, strong correlations have not always been found between performance on face tasks and clinical measure of function. Based on the evidence of abnormal eye movements by patients with age-related macular degeneration (AMD), we explored whether abnormal fixation patterns occur when these patients view an image of a face. METHODS: An OPKO OCT/SLO was used to collect structural and functional data. For each subject, the structural location of disease was determined, and the locus and stability of fixation were quantified. A SLO movie of fundus movements was recorded while the subject viewed an image of a face. RESULTS: The number of fixations on internal (eyes, nose, and mouth) and external features were measured. A two-way repeated-measures analysis of variance found significant differences between the control and patient groups and among locations. A significant interaction between group and location was also found. Post hoc comparisons found a significantly greater proportion of fixations on external features for the AMD group than that in the control group. CONCLUSIONS: The observed patterns of fixations of our subjects with AMD were similar to those observed in other groups of patients who have difficulties with face perception. For example, individuals with social phobias, Williams syndrome, autism, schizophrenia, or prosopagnosia have altered face perceptions and also have a significantly greater proportion of fixations on external features of faces. Abnormal eye movement patterns and fixations may contribute to deficits in face perception in AMD patients.
PMID: 23238260
ISSN: 1040-5488
CID: 220732