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Anatomic–Functional Correlates in Lesions of Retinal Vein Occlusion

PURPOSE: To evaluate anatomic–functional associations at sites of retinal lesions in retinal vein occlusion (RVO). METHODS: This pilot, prospective, observational study was conducted at the Northern Ireland Clinical Research Facility (NICRF) of Queen's University and the Belfast Health and Soci...

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Autores principales: Khayat, Meiaad, Perais, Jennifer, Wright, David M., Williams, Michael, Lois, Noemi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196416/
https://www.ncbi.nlm.nih.gov/pubmed/34100891
http://dx.doi.org/10.1167/iovs.62.7.10
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author Khayat, Meiaad
Perais, Jennifer
Wright, David M.
Williams, Michael
Lois, Noemi
author_facet Khayat, Meiaad
Perais, Jennifer
Wright, David M.
Williams, Michael
Lois, Noemi
author_sort Khayat, Meiaad
collection PubMed
description PURPOSE: To evaluate anatomic–functional associations at sites of retinal lesions in retinal vein occlusion (RVO). METHODS: This pilot, prospective, observational study was conducted at the Northern Ireland Clinical Research Facility (NICRF) of Queen's University and the Belfast Health and Social Care Trust, Northern Ireland, between August 1, 2018, and September 30, 2019. The study included 10 treatment-naïve patients with RVO (10 RVO eyes and 10 fellow eyes). There were 81 points/sites assessed for each eye at baseline; six patients were re-assessed 6 months after anti-vascular endothelial growth factor therapy at the same locations. We investigated associations between retinal sensitivity and presence of structural RVO lesions, including retinal ischemia, hemorrhages, intraretinal fluid (IRF) and subretinal fluid outside the foveal/parafoveal regions. Comparisons were made between RVO eyes and fellow eyes at baseline, and between RVO eyes at baseline and at 6 months after treatment. Regression models were used to investigate anatomic–functional associations. RESULTS: At baseline, strong associations were found between reduced retinal sensitivity and presence of ischemia (estimate = −2.08 dB; P < 0.001), intraretinal fluid (estimate = −7.82 dB; P < 0.001), and subretinal fluid (estimate = −8.66 dB; P < 0.001). Resolution of subretinal fluid but not intraretinal fluid was associated with improved function (estimate = 2.40 dB [P = 0.022]; estimate = 1.16 dB [P = 0.228], respectively). However, reperfusion of ischemic retina, observed in 31 of 486 points (6%) 6 months after anti-vascular endothelial growth factor therapy, was associated with a further decrease in retinal sensitivity (estimate = −2.34 dB; P = 0.035). CONCLUSIONS: Retinal sensitivity was decreased at sites of RVO lesions. Decreased function at sites of retinal ischemia did not recover after treatment, even when reperfusion occurred.
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spelling pubmed-81964162021-06-22 Anatomic–Functional Correlates in Lesions of Retinal Vein Occlusion Khayat, Meiaad Perais, Jennifer Wright, David M. Williams, Michael Lois, Noemi Invest Ophthalmol Vis Sci Retina PURPOSE: To evaluate anatomic–functional associations at sites of retinal lesions in retinal vein occlusion (RVO). METHODS: This pilot, prospective, observational study was conducted at the Northern Ireland Clinical Research Facility (NICRF) of Queen's University and the Belfast Health and Social Care Trust, Northern Ireland, between August 1, 2018, and September 30, 2019. The study included 10 treatment-naïve patients with RVO (10 RVO eyes and 10 fellow eyes). There were 81 points/sites assessed for each eye at baseline; six patients were re-assessed 6 months after anti-vascular endothelial growth factor therapy at the same locations. We investigated associations between retinal sensitivity and presence of structural RVO lesions, including retinal ischemia, hemorrhages, intraretinal fluid (IRF) and subretinal fluid outside the foveal/parafoveal regions. Comparisons were made between RVO eyes and fellow eyes at baseline, and between RVO eyes at baseline and at 6 months after treatment. Regression models were used to investigate anatomic–functional associations. RESULTS: At baseline, strong associations were found between reduced retinal sensitivity and presence of ischemia (estimate = −2.08 dB; P < 0.001), intraretinal fluid (estimate = −7.82 dB; P < 0.001), and subretinal fluid (estimate = −8.66 dB; P < 0.001). Resolution of subretinal fluid but not intraretinal fluid was associated with improved function (estimate = 2.40 dB [P = 0.022]; estimate = 1.16 dB [P = 0.228], respectively). However, reperfusion of ischemic retina, observed in 31 of 486 points (6%) 6 months after anti-vascular endothelial growth factor therapy, was associated with a further decrease in retinal sensitivity (estimate = −2.34 dB; P = 0.035). CONCLUSIONS: Retinal sensitivity was decreased at sites of RVO lesions. Decreased function at sites of retinal ischemia did not recover after treatment, even when reperfusion occurred. The Association for Research in Vision and Ophthalmology 2021-06-08 /pmc/articles/PMC8196416/ /pubmed/34100891 http://dx.doi.org/10.1167/iovs.62.7.10 Text en Copyright 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Retina
Khayat, Meiaad
Perais, Jennifer
Wright, David M.
Williams, Michael
Lois, Noemi
Anatomic–Functional Correlates in Lesions of Retinal Vein Occlusion
title Anatomic–Functional Correlates in Lesions of Retinal Vein Occlusion
title_full Anatomic–Functional Correlates in Lesions of Retinal Vein Occlusion
title_fullStr Anatomic–Functional Correlates in Lesions of Retinal Vein Occlusion
title_full_unstemmed Anatomic–Functional Correlates in Lesions of Retinal Vein Occlusion
title_short Anatomic–Functional Correlates in Lesions of Retinal Vein Occlusion
title_sort anatomic–functional correlates in lesions of retinal vein occlusion
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196416/
https://www.ncbi.nlm.nih.gov/pubmed/34100891
http://dx.doi.org/10.1167/iovs.62.7.10
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