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Optic Disc Hemorrhage Is Related to Various Hemodynamic Findings by Disc Angiography

BACKGROUND: To investigate the hemodynamic characteristics of glaucoma eyes with disc hemorrhage (DH) by disc fluorescein angiography, and its relationship with glaucomatous changes of the optic disc and surrounding retinal nerve fiber layer (RNFL). METHODS: This study included 35 glaucoma eyes with...

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Autores principales: Park, Hae Young Lopilly, Jeong, Hyun Jin, Kim, Yoon Hee, Park, Chan Kee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400035/
https://www.ncbi.nlm.nih.gov/pubmed/25879852
http://dx.doi.org/10.1371/journal.pone.0120000
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author Park, Hae Young Lopilly
Jeong, Hyun Jin
Kim, Yoon Hee
Park, Chan Kee
author_facet Park, Hae Young Lopilly
Jeong, Hyun Jin
Kim, Yoon Hee
Park, Chan Kee
author_sort Park, Hae Young Lopilly
collection PubMed
description BACKGROUND: To investigate the hemodynamic characteristics of glaucoma eyes with disc hemorrhage (DH) by disc fluorescein angiography, and its relationship with glaucomatous changes of the optic disc and surrounding retinal nerve fiber layer (RNFL). METHODS: This study included 35 glaucoma eyes with DH who were followed up at least 5 years and had DH at presentation. Eyes were classified as eyes with DH at the border of localized RNFL defects and eyes with DH not related to localized RNFL defects. Prevalence of DH and location of the proximal border were recorded from disc photographs. Fluorescein angiography was performed 3 months after detecting the DH. Arm-retina time, arteriovenous transit time, disc filling time, choroidal filling time, and venous filling time were measured as retinal circulation parameters. The presence of disc filling defects and disc leaks were evaluated. RESULTS: There were 19 (54.3%) eyes with DH accompanying localized RNFL defects. The arm-retina time was prolonged in eyes with DH not related to RNFL defects (P = 0.044) and the arteriovenous transit time was prolonged in eyes with DH accompanying RNFL defects (P = 0.029). Among eyes with DH accompanying RNFL defects, 11 (57.9%) had vessel filling defects or delayed filling indicating blood flow stasis at the cup margin proximal to where DH occurred. Eyes with DH not related to RNFL defects did not show vessel filling defects or delayed filling. CONCLUSIONS AND RELEVANCE: Eyes with DH related to RNFL defects showed prolonged arteriovenous transit time and had frequent vessel filling defects or delayed filling indicating blood flow stasis and thrombus formation at the site DH occurred. These findings suggest that vascular and hemodynamic changes due to glaucomatous structural changes cause DH in relation to localized RNFL defects.
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spelling pubmed-44000352015-04-21 Optic Disc Hemorrhage Is Related to Various Hemodynamic Findings by Disc Angiography Park, Hae Young Lopilly Jeong, Hyun Jin Kim, Yoon Hee Park, Chan Kee PLoS One Research Article BACKGROUND: To investigate the hemodynamic characteristics of glaucoma eyes with disc hemorrhage (DH) by disc fluorescein angiography, and its relationship with glaucomatous changes of the optic disc and surrounding retinal nerve fiber layer (RNFL). METHODS: This study included 35 glaucoma eyes with DH who were followed up at least 5 years and had DH at presentation. Eyes were classified as eyes with DH at the border of localized RNFL defects and eyes with DH not related to localized RNFL defects. Prevalence of DH and location of the proximal border were recorded from disc photographs. Fluorescein angiography was performed 3 months after detecting the DH. Arm-retina time, arteriovenous transit time, disc filling time, choroidal filling time, and venous filling time were measured as retinal circulation parameters. The presence of disc filling defects and disc leaks were evaluated. RESULTS: There were 19 (54.3%) eyes with DH accompanying localized RNFL defects. The arm-retina time was prolonged in eyes with DH not related to RNFL defects (P = 0.044) and the arteriovenous transit time was prolonged in eyes with DH accompanying RNFL defects (P = 0.029). Among eyes with DH accompanying RNFL defects, 11 (57.9%) had vessel filling defects or delayed filling indicating blood flow stasis at the cup margin proximal to where DH occurred. Eyes with DH not related to RNFL defects did not show vessel filling defects or delayed filling. CONCLUSIONS AND RELEVANCE: Eyes with DH related to RNFL defects showed prolonged arteriovenous transit time and had frequent vessel filling defects or delayed filling indicating blood flow stasis and thrombus formation at the site DH occurred. These findings suggest that vascular and hemodynamic changes due to glaucomatous structural changes cause DH in relation to localized RNFL defects. Public Library of Science 2015-04-16 /pmc/articles/PMC4400035/ /pubmed/25879852 http://dx.doi.org/10.1371/journal.pone.0120000 Text en © 2015 Park et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Park, Hae Young Lopilly
Jeong, Hyun Jin
Kim, Yoon Hee
Park, Chan Kee
Optic Disc Hemorrhage Is Related to Various Hemodynamic Findings by Disc Angiography
title Optic Disc Hemorrhage Is Related to Various Hemodynamic Findings by Disc Angiography
title_full Optic Disc Hemorrhage Is Related to Various Hemodynamic Findings by Disc Angiography
title_fullStr Optic Disc Hemorrhage Is Related to Various Hemodynamic Findings by Disc Angiography
title_full_unstemmed Optic Disc Hemorrhage Is Related to Various Hemodynamic Findings by Disc Angiography
title_short Optic Disc Hemorrhage Is Related to Various Hemodynamic Findings by Disc Angiography
title_sort optic disc hemorrhage is related to various hemodynamic findings by disc angiography
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400035/
https://www.ncbi.nlm.nih.gov/pubmed/25879852
http://dx.doi.org/10.1371/journal.pone.0120000
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