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Deep Defects Seen on Visual Fields Spatially Correspond Well to Loss of Retinal Nerve Fiber Layer Seen on Circumpapillary OCT Scans

PURPOSE: To examine the structure–function relationship in glaucoma between deep defects on visual fields (VF) and deep losses in the circumpapillary retinal nerve fiber layer (cpRNFL) on optical coherence tomography (OCT) circle scans. METHODS: Thirty two glaucomatous eyes with deep VF defects, as...

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Autores principales: Mavrommatis, Maria A., Wu, Zhichao, Naegele, Saskia I., Nunez, Jason, de Moraes, Gustavo C., Ritch, Robert, Hood, Donald C.
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/PMC5795898/
https://www.ncbi.nlm.nih.gov/pubmed/29392306
http://dx.doi.org/10.1167/iovs.17-23097
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author Mavrommatis, Maria A.
Wu, Zhichao
Naegele, Saskia I.
Nunez, Jason
de Moraes, Gustavo C.
Ritch, Robert
Hood, Donald C.
author_facet Mavrommatis, Maria A.
Wu, Zhichao
Naegele, Saskia I.
Nunez, Jason
de Moraes, Gustavo C.
Ritch, Robert
Hood, Donald C.
author_sort Mavrommatis, Maria A.
collection PubMed
description PURPOSE: To examine the structure–function relationship in glaucoma between deep defects on visual fields (VF) and deep losses in the circumpapillary retinal nerve fiber layer (cpRNFL) on optical coherence tomography (OCT) circle scans. METHODS: Thirty two glaucomatous eyes with deep VF defects, as defined by at least one test location worse than ≤ −15 dB on the 10-2 and/or 24-2 VF pattern deviation (PD) plots, were included from 87 eyes with “early” glaucoma (i.e., 24-2 mean deviation better than −6 dB). Using the location of the deep VF points and a schematic model, the location of local damage on an OCT circle scan was predicted. The thinnest location of cpRNFL (i.e., deepest loss) was also determined. RESULTS: In 19 of 32 eyes, a region of complete or near complete cpRNFL loss was observed. All 19 of these had deep VF defects on the 24-2 and/or 10-2. All of the 32 eyes with deep VF defects had abnormal cpRNFL regions (red, 1%) and all but 2 had a region of cpRNFL thickness <21 μm. The midpoint of the VF defect and the location of deepest cpRNFL had a 95% limit of agreement within approximately two-thirds of a clock-hour (or 30°) sector (between −22.1° to 25.2°). Individual fovea-to-disc angle (FtoDa) adjustment improved agreement in one eye with an extreme FtoDa. CONCLUSIONS: Although studies relating local structural (OCT) and functional (VF) measures typically show poor to moderate correlations, there is good qualitative agreement between the location of deep cpRNFL loss and deep defects on VFs.
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spelling pubmed-57958982018-02-06 Deep Defects Seen on Visual Fields Spatially Correspond Well to Loss of Retinal Nerve Fiber Layer Seen on Circumpapillary OCT Scans Mavrommatis, Maria A. Wu, Zhichao Naegele, Saskia I. Nunez, Jason de Moraes, Gustavo C. Ritch, Robert Hood, Donald C. Invest Ophthalmol Vis Sci Glaucoma PURPOSE: To examine the structure–function relationship in glaucoma between deep defects on visual fields (VF) and deep losses in the circumpapillary retinal nerve fiber layer (cpRNFL) on optical coherence tomography (OCT) circle scans. METHODS: Thirty two glaucomatous eyes with deep VF defects, as defined by at least one test location worse than ≤ −15 dB on the 10-2 and/or 24-2 VF pattern deviation (PD) plots, were included from 87 eyes with “early” glaucoma (i.e., 24-2 mean deviation better than −6 dB). Using the location of the deep VF points and a schematic model, the location of local damage on an OCT circle scan was predicted. The thinnest location of cpRNFL (i.e., deepest loss) was also determined. RESULTS: In 19 of 32 eyes, a region of complete or near complete cpRNFL loss was observed. All 19 of these had deep VF defects on the 24-2 and/or 10-2. All of the 32 eyes with deep VF defects had abnormal cpRNFL regions (red, 1%) and all but 2 had a region of cpRNFL thickness <21 μm. The midpoint of the VF defect and the location of deepest cpRNFL had a 95% limit of agreement within approximately two-thirds of a clock-hour (or 30°) sector (between −22.1° to 25.2°). Individual fovea-to-disc angle (FtoDa) adjustment improved agreement in one eye with an extreme FtoDa. CONCLUSIONS: Although studies relating local structural (OCT) and functional (VF) measures typically show poor to moderate correlations, there is good qualitative agreement between the location of deep cpRNFL loss and deep defects on VFs. The Association for Research in Vision and Ophthalmology 2018-02 /pmc/articles/PMC5795898/ /pubmed/29392306 http://dx.doi.org/10.1167/iovs.17-23097 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 Glaucoma
Mavrommatis, Maria A.
Wu, Zhichao
Naegele, Saskia I.
Nunez, Jason
de Moraes, Gustavo C.
Ritch, Robert
Hood, Donald C.
Deep Defects Seen on Visual Fields Spatially Correspond Well to Loss of Retinal Nerve Fiber Layer Seen on Circumpapillary OCT Scans
title Deep Defects Seen on Visual Fields Spatially Correspond Well to Loss of Retinal Nerve Fiber Layer Seen on Circumpapillary OCT Scans
title_full Deep Defects Seen on Visual Fields Spatially Correspond Well to Loss of Retinal Nerve Fiber Layer Seen on Circumpapillary OCT Scans
title_fullStr Deep Defects Seen on Visual Fields Spatially Correspond Well to Loss of Retinal Nerve Fiber Layer Seen on Circumpapillary OCT Scans
title_full_unstemmed Deep Defects Seen on Visual Fields Spatially Correspond Well to Loss of Retinal Nerve Fiber Layer Seen on Circumpapillary OCT Scans
title_short Deep Defects Seen on Visual Fields Spatially Correspond Well to Loss of Retinal Nerve Fiber Layer Seen on Circumpapillary OCT Scans
title_sort deep defects seen on visual fields spatially correspond well to loss of retinal nerve fiber layer seen on circumpapillary oct scans
topic Glaucoma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5795898/
https://www.ncbi.nlm.nih.gov/pubmed/29392306
http://dx.doi.org/10.1167/iovs.17-23097
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