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Homonymous visual field defect and retinal thinning after occipital stroke

INTRODUCTION: Stroke is the most common cause of homonymous visual field defects (VFD). About half of the stroke patients recover from VFD. However, relationship between VFD and retinal changes remains elusive. PURPOSE: To investigate the association between occurrence of VFD, changes of macular gan...

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Autores principales: Rashid, Avan Sabir, Rashid, Darian, Yang, Ge, Link, Hans, Gauffin, Helena, Huang‐Link, Yumin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553301/
https://www.ncbi.nlm.nih.gov/pubmed/34487632
http://dx.doi.org/10.1002/brb3.2345
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author Rashid, Avan Sabir
Rashid, Darian
Yang, Ge
Link, Hans
Gauffin, Helena
Huang‐Link, Yumin
author_facet Rashid, Avan Sabir
Rashid, Darian
Yang, Ge
Link, Hans
Gauffin, Helena
Huang‐Link, Yumin
author_sort Rashid, Avan Sabir
collection PubMed
description INTRODUCTION: Stroke is the most common cause of homonymous visual field defects (VFD). About half of the stroke patients recover from VFD. However, relationship between VFD and retinal changes remains elusive. PURPOSE: To investigate the association between occurrence of VFD, changes of macular ganglion cell and inner plexiform layer (GCIPL) and its axon retinal nerve fiber layer (RNFL) detected with optical coherence tomography (OCT). PATIENTS AND METHODS: The study consists of retrospective review of medical records and follow‐up examinations. Patients with acute occipital stroke were registered. VFD was identified with confrontation and/or perimetry tests at the onset. At follow‐up, the patients were examined with visual field tests and OCT measurements. RESULTS: Thirty‐six patients met the inclusion criteria. At onset, 26 patients (72%) had VFD. At follow‐up >1 year after stroke, 13 patients (36%) had remaining VFD: 5 had homonymous hemianopia, 5 had homonymous quadrantanopia, and 3 had homonymous scotomas. Average thickness of GCIPL and RNFL were significantly reduced in each eye in patients with VFD compared to non‐VFD (NVFD) (p < .01 for all comparisons). Thickness of superior and inferior RNFL quadrants was significantly reduced in VFD compared to NVFD (p < .01 for both). Among these 13 patients, 4 had characteristic homonymous quadrant‐GCIPL thinning, 2 had characteristic homonymous hemi‐GCIPL thinning, and 7 had diffuse GCIPL thinning. CONCLUSION: GCIPL and RNFL thinning were observed in the patients with VFD. GCIPL thinning appears in two forms: atypical diffuse thinning, or homonymous hemi‐GCIPL thinning. Examining GCIPL and RNFL provides easy and reliable objective measures and is therefore proposed to be of predictive value on visual function.
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spelling pubmed-85533012021-11-04 Homonymous visual field defect and retinal thinning after occipital stroke Rashid, Avan Sabir Rashid, Darian Yang, Ge Link, Hans Gauffin, Helena Huang‐Link, Yumin Brain Behav Original Articles INTRODUCTION: Stroke is the most common cause of homonymous visual field defects (VFD). About half of the stroke patients recover from VFD. However, relationship between VFD and retinal changes remains elusive. PURPOSE: To investigate the association between occurrence of VFD, changes of macular ganglion cell and inner plexiform layer (GCIPL) and its axon retinal nerve fiber layer (RNFL) detected with optical coherence tomography (OCT). PATIENTS AND METHODS: The study consists of retrospective review of medical records and follow‐up examinations. Patients with acute occipital stroke were registered. VFD was identified with confrontation and/or perimetry tests at the onset. At follow‐up, the patients were examined with visual field tests and OCT measurements. RESULTS: Thirty‐six patients met the inclusion criteria. At onset, 26 patients (72%) had VFD. At follow‐up >1 year after stroke, 13 patients (36%) had remaining VFD: 5 had homonymous hemianopia, 5 had homonymous quadrantanopia, and 3 had homonymous scotomas. Average thickness of GCIPL and RNFL were significantly reduced in each eye in patients with VFD compared to non‐VFD (NVFD) (p < .01 for all comparisons). Thickness of superior and inferior RNFL quadrants was significantly reduced in VFD compared to NVFD (p < .01 for both). Among these 13 patients, 4 had characteristic homonymous quadrant‐GCIPL thinning, 2 had characteristic homonymous hemi‐GCIPL thinning, and 7 had diffuse GCIPL thinning. CONCLUSION: GCIPL and RNFL thinning were observed in the patients with VFD. GCIPL thinning appears in two forms: atypical diffuse thinning, or homonymous hemi‐GCIPL thinning. Examining GCIPL and RNFL provides easy and reliable objective measures and is therefore proposed to be of predictive value on visual function. John Wiley and Sons Inc. 2021-09-06 /pmc/articles/PMC8553301/ /pubmed/34487632 http://dx.doi.org/10.1002/brb3.2345 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rashid, Avan Sabir
Rashid, Darian
Yang, Ge
Link, Hans
Gauffin, Helena
Huang‐Link, Yumin
Homonymous visual field defect and retinal thinning after occipital stroke
title Homonymous visual field defect and retinal thinning after occipital stroke
title_full Homonymous visual field defect and retinal thinning after occipital stroke
title_fullStr Homonymous visual field defect and retinal thinning after occipital stroke
title_full_unstemmed Homonymous visual field defect and retinal thinning after occipital stroke
title_short Homonymous visual field defect and retinal thinning after occipital stroke
title_sort homonymous visual field defect and retinal thinning after occipital stroke
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553301/
https://www.ncbi.nlm.nih.gov/pubmed/34487632
http://dx.doi.org/10.1002/brb3.2345
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