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A Method Using Goldmann Stimulus Sizes I to V–Measured Sensitivities to Predict Lead Time Gained to Visual Field Defect Detection in Early Glaucoma

PURPOSE: To predict the lead time (difference in time taken for a visual field [VF] defect to be detected) obtained when using stimulus sizes within or near the size of the critical area of spatial summation (Ac), and to test these predictions using sensitivity measurements from a cohort of glaucoma...

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Autores principales: Phu, Jack, Khuu, Sieu K., Bui, Bang V., Kalloniatis, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993363/
https://www.ncbi.nlm.nih.gov/pubmed/29892496
http://dx.doi.org/10.1167/tvst.7.3.17
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author Phu, Jack
Khuu, Sieu K.
Bui, Bang V.
Kalloniatis, Michael
author_facet Phu, Jack
Khuu, Sieu K.
Bui, Bang V.
Kalloniatis, Michael
author_sort Phu, Jack
collection PubMed
description PURPOSE: To predict the lead time (difference in time taken for a visual field [VF] defect to be detected) obtained when using stimulus sizes within or near the size of the critical area of spatial summation (Ac), and to test these predictions using sensitivity measurements from a cohort of glaucoma patients. METHODS: Thirty-seven patients with early open-angle glaucoma and 60 healthy observers underwent VF testing on the Humphrey Field Analyzer in full threshold mode using Goldmann stimulus sizes I to V (GI–V) across the 30-2 test grid. We used the sensitivities measured using GI to V in healthy patients to predict the lead time gained by using stimulus sizes within the size of Ac at all locations within the 30-2 grid. Then, we used sensitivities measured in the glaucoma patients to test this predictive model. RESULTS: Median lead time to VF defect detection when using stimulus sizes within Ac compared with stimulus sizes larger than Ac was 4.1 years across the 30-2 test grid (interquartile range, 3.1 and 5.1 years). Sensitivities of the glaucoma patients showed good agreement with the predictive model of lead time gained (77.5%–84.3% were within ±3 dB). CONCLUSIONS: Our model predicted substantial lead time differences when using stimulus sizes within or near Ac. Such stimulus sizes could potentially detect VF defects, on average, 4 years earlier than current paradigms. TRANSLATIONAL RELEVANCE: Stimulus sizes within or near Ac may be more suitable for early detection of glaucomatous VF defects. Larger stimulus sizes may be more suitable for later monitoring of established disease.
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spelling pubmed-59933632018-06-11 A Method Using Goldmann Stimulus Sizes I to V–Measured Sensitivities to Predict Lead Time Gained to Visual Field Defect Detection in Early Glaucoma Phu, Jack Khuu, Sieu K. Bui, Bang V. Kalloniatis, Michael Transl Vis Sci Technol Articles PURPOSE: To predict the lead time (difference in time taken for a visual field [VF] defect to be detected) obtained when using stimulus sizes within or near the size of the critical area of spatial summation (Ac), and to test these predictions using sensitivity measurements from a cohort of glaucoma patients. METHODS: Thirty-seven patients with early open-angle glaucoma and 60 healthy observers underwent VF testing on the Humphrey Field Analyzer in full threshold mode using Goldmann stimulus sizes I to V (GI–V) across the 30-2 test grid. We used the sensitivities measured using GI to V in healthy patients to predict the lead time gained by using stimulus sizes within the size of Ac at all locations within the 30-2 grid. Then, we used sensitivities measured in the glaucoma patients to test this predictive model. RESULTS: Median lead time to VF defect detection when using stimulus sizes within Ac compared with stimulus sizes larger than Ac was 4.1 years across the 30-2 test grid (interquartile range, 3.1 and 5.1 years). Sensitivities of the glaucoma patients showed good agreement with the predictive model of lead time gained (77.5%–84.3% were within ±3 dB). CONCLUSIONS: Our model predicted substantial lead time differences when using stimulus sizes within or near Ac. Such stimulus sizes could potentially detect VF defects, on average, 4 years earlier than current paradigms. TRANSLATIONAL RELEVANCE: Stimulus sizes within or near Ac may be more suitable for early detection of glaucomatous VF defects. Larger stimulus sizes may be more suitable for later monitoring of established disease. The Association for Research in Vision and Ophthalmology 2018-06-07 /pmc/articles/PMC5993363/ /pubmed/29892496 http://dx.doi.org/10.1167/tvst.7.3.17 Text en Copyright 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Articles
Phu, Jack
Khuu, Sieu K.
Bui, Bang V.
Kalloniatis, Michael
A Method Using Goldmann Stimulus Sizes I to V–Measured Sensitivities to Predict Lead Time Gained to Visual Field Defect Detection in Early Glaucoma
title A Method Using Goldmann Stimulus Sizes I to V–Measured Sensitivities to Predict Lead Time Gained to Visual Field Defect Detection in Early Glaucoma
title_full A Method Using Goldmann Stimulus Sizes I to V–Measured Sensitivities to Predict Lead Time Gained to Visual Field Defect Detection in Early Glaucoma
title_fullStr A Method Using Goldmann Stimulus Sizes I to V–Measured Sensitivities to Predict Lead Time Gained to Visual Field Defect Detection in Early Glaucoma
title_full_unstemmed A Method Using Goldmann Stimulus Sizes I to V–Measured Sensitivities to Predict Lead Time Gained to Visual Field Defect Detection in Early Glaucoma
title_short A Method Using Goldmann Stimulus Sizes I to V–Measured Sensitivities to Predict Lead Time Gained to Visual Field Defect Detection in Early Glaucoma
title_sort method using goldmann stimulus sizes i to v–measured sensitivities to predict lead time gained to visual field defect detection in early glaucoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993363/
https://www.ncbi.nlm.nih.gov/pubmed/29892496
http://dx.doi.org/10.1167/tvst.7.3.17
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