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Foveal Damage Due to Subfoveal Hemorrhage Associated with Branch Retinal Vein Occlusion

To investigate the functional and morphologic prognoses of eyes with subfoveal hemorrhage from acute branch retinal vein occlusion (BRVO), and to examine the effect of intravitreal ranibizumab injection (IVR) on these prognoses, we assessed 81 eyes with acute BRVO, of which 38 did not receive IVR [I...

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Autores principales: Muraoka, Yuki, Tsujikawa, Akitaka, Takahashi, Ayako, Iida, Yuto, Murakami, Tomoaki, Ooto, Sotaro, Suzuma, Kiyoshi, Uji, Akihito, Yoshimura, Nagahisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677927/
https://www.ncbi.nlm.nih.gov/pubmed/26661582
http://dx.doi.org/10.1371/journal.pone.0144894
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author Muraoka, Yuki
Tsujikawa, Akitaka
Takahashi, Ayako
Iida, Yuto
Murakami, Tomoaki
Ooto, Sotaro
Suzuma, Kiyoshi
Uji, Akihito
Yoshimura, Nagahisa
author_facet Muraoka, Yuki
Tsujikawa, Akitaka
Takahashi, Ayako
Iida, Yuto
Murakami, Tomoaki
Ooto, Sotaro
Suzuma, Kiyoshi
Uji, Akihito
Yoshimura, Nagahisa
author_sort Muraoka, Yuki
collection PubMed
description To investigate the functional and morphologic prognoses of eyes with subfoveal hemorrhage from acute branch retinal vein occlusion (BRVO), and to examine the effect of intravitreal ranibizumab injection (IVR) on these prognoses, we assessed 81 eyes with acute BRVO, of which 38 did not receive IVR [IVR(-) group], and 43 were treated with IVR [IVR(+) group] for macular edema. The foveal morphologic changes were examined via optical coherence tomography (OCT). At initial examination, 63 eyes exhibited subfoveal hemorrhage. At final examination, the defect lengths in the foveal external limiting membrane (ELM) and ellipsoid lines in these eyes were longer, and final VA was significantly poorer, compared with eyes without subfoveal hemorrhage. In comparisons between the final measurements in eyes with subfoveal hemorrhage in the IVR(-) and IVR(+) groups, while there were no differences in initial ocular conditions, final VA was significantly better in the IVR(+) group. The defects in the ELM and ellipsoid lines in the IVR(+) group were shorter than those of the IVR(-) group (p = 0.002 in both). Final VA was correlated with the defect lengths of foveal ELM and ellipsoid lines in both the IVR(-) and IVR(+) groups (both p < 0.001). In addition, the defect lengths of foveal ELM and ellipsoid lines were closely correlated with the duration of subfoveal hemorrhage (both p < 0.001). BRVO-associated subfoveal hemorrhage caused damage to the foveal photoreceptors, and visual dysfunction. However, IVR improved these prognoses, by accelerating the absorption of the subfoveal hemorrhage.
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spelling pubmed-46779272015-12-31 Foveal Damage Due to Subfoveal Hemorrhage Associated with Branch Retinal Vein Occlusion Muraoka, Yuki Tsujikawa, Akitaka Takahashi, Ayako Iida, Yuto Murakami, Tomoaki Ooto, Sotaro Suzuma, Kiyoshi Uji, Akihito Yoshimura, Nagahisa PLoS One Research Article To investigate the functional and morphologic prognoses of eyes with subfoveal hemorrhage from acute branch retinal vein occlusion (BRVO), and to examine the effect of intravitreal ranibizumab injection (IVR) on these prognoses, we assessed 81 eyes with acute BRVO, of which 38 did not receive IVR [IVR(-) group], and 43 were treated with IVR [IVR(+) group] for macular edema. The foveal morphologic changes were examined via optical coherence tomography (OCT). At initial examination, 63 eyes exhibited subfoveal hemorrhage. At final examination, the defect lengths in the foveal external limiting membrane (ELM) and ellipsoid lines in these eyes were longer, and final VA was significantly poorer, compared with eyes without subfoveal hemorrhage. In comparisons between the final measurements in eyes with subfoveal hemorrhage in the IVR(-) and IVR(+) groups, while there were no differences in initial ocular conditions, final VA was significantly better in the IVR(+) group. The defects in the ELM and ellipsoid lines in the IVR(+) group were shorter than those of the IVR(-) group (p = 0.002 in both). Final VA was correlated with the defect lengths of foveal ELM and ellipsoid lines in both the IVR(-) and IVR(+) groups (both p < 0.001). In addition, the defect lengths of foveal ELM and ellipsoid lines were closely correlated with the duration of subfoveal hemorrhage (both p < 0.001). BRVO-associated subfoveal hemorrhage caused damage to the foveal photoreceptors, and visual dysfunction. However, IVR improved these prognoses, by accelerating the absorption of the subfoveal hemorrhage. Public Library of Science 2015-12-14 /pmc/articles/PMC4677927/ /pubmed/26661582 http://dx.doi.org/10.1371/journal.pone.0144894 Text en © 2015 Muraoka 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
Muraoka, Yuki
Tsujikawa, Akitaka
Takahashi, Ayako
Iida, Yuto
Murakami, Tomoaki
Ooto, Sotaro
Suzuma, Kiyoshi
Uji, Akihito
Yoshimura, Nagahisa
Foveal Damage Due to Subfoveal Hemorrhage Associated with Branch Retinal Vein Occlusion
title Foveal Damage Due to Subfoveal Hemorrhage Associated with Branch Retinal Vein Occlusion
title_full Foveal Damage Due to Subfoveal Hemorrhage Associated with Branch Retinal Vein Occlusion
title_fullStr Foveal Damage Due to Subfoveal Hemorrhage Associated with Branch Retinal Vein Occlusion
title_full_unstemmed Foveal Damage Due to Subfoveal Hemorrhage Associated with Branch Retinal Vein Occlusion
title_short Foveal Damage Due to Subfoveal Hemorrhage Associated with Branch Retinal Vein Occlusion
title_sort foveal damage due to subfoveal hemorrhage associated with branch retinal vein occlusion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677927/
https://www.ncbi.nlm.nih.gov/pubmed/26661582
http://dx.doi.org/10.1371/journal.pone.0144894
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