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Ranibizumab therapy for predominantly hemorrhagic neovascular age-related macular degeneration
OBJECTIVE: Predominantly hemorrhage represents one of the possible manifestations of choroidal neovascularisation (CNV) in eyes with age-related macular degeneration (AMD). The purpose of this study is to evaluate the effecte of ranibizumab treatment in patients with predominantly hemorrhagic CNV se...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Health Directorate of Istanbul
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039638/ https://www.ncbi.nlm.nih.gov/pubmed/35582510 http://dx.doi.org/10.14744/nci.2021.52323 |
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author | Dikmetas, Ozlem Kadayifcilar, Sibel Eldem, Bora Feyzullayeva, Ulkar |
author_facet | Dikmetas, Ozlem Kadayifcilar, Sibel Eldem, Bora Feyzullayeva, Ulkar |
author_sort | Dikmetas, Ozlem |
collection | PubMed |
description | OBJECTIVE: Predominantly hemorrhage represents one of the possible manifestations of choroidal neovascularisation (CNV) in eyes with age-related macular degeneration (AMD). The purpose of this study is to evaluate the effecte of ranibizumab treatment in patients with predominantly hemorrhagic CNV secondary to AMD. METHODS: Twenty-five patients with predominantly hemorrhagic choroidal neovascularization due to AMD with at least three ranibizumab injections and followed up for at least 12 months were included in the study. The months of follow-up were recorded (baseline, 3(rd), 6(th), and 12(th) months). The change in central macular thickness (CMT) on optical coherence tomography, visual acuity (VA) in ETDRS letters, and lesion size on fundus fluorescein angiography were evaluated. RESULTS: The mean age of the patients was 68.1±5.7 (range: 63–82) years, the mean follow-up was 19.9±14.5 (range: 12–67) months, and the mean number of injections was 4.0±1.4 (range: 3–15). The initial VA was 39.3±17.9 (range: 1–65) letters, CMT was 272.7±104 (range: 164–587) μm, and the initial lesion width was 11.4±10.5 (range: 1.3–45.7) mm(2). The VA was 41.4±20.1 (range: 5–75) and 36.9±21.8 (range: 4–80) letters (p=0.150), CMT was 270.7±110 (range: 159–570) and 230.4±108 (range: 109–667) μm (p=0.009) and the lesion width was 10.9±11.5 (range: 1.1–39.7) and 10.4±11.6 (range: 1.2–44.3) mm(2) at 6(th) and 12(th) month, respectively. No factor was found to be associated with final CMT. CONCLUSION: Although the final visual outcome is limited by the progression of the disease, hemorrhagic lesions treated with ranibizumab have stable anatomical outcome. |
format | Online Article Text |
id | pubmed-9039638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Health Directorate of Istanbul |
record_format | MEDLINE/PubMed |
spelling | pubmed-90396382022-05-16 Ranibizumab therapy for predominantly hemorrhagic neovascular age-related macular degeneration Dikmetas, Ozlem Kadayifcilar, Sibel Eldem, Bora Feyzullayeva, Ulkar North Clin Istanb Original Article - Ophthalmology OBJECTIVE: Predominantly hemorrhage represents one of the possible manifestations of choroidal neovascularisation (CNV) in eyes with age-related macular degeneration (AMD). The purpose of this study is to evaluate the effecte of ranibizumab treatment in patients with predominantly hemorrhagic CNV secondary to AMD. METHODS: Twenty-five patients with predominantly hemorrhagic choroidal neovascularization due to AMD with at least three ranibizumab injections and followed up for at least 12 months were included in the study. The months of follow-up were recorded (baseline, 3(rd), 6(th), and 12(th) months). The change in central macular thickness (CMT) on optical coherence tomography, visual acuity (VA) in ETDRS letters, and lesion size on fundus fluorescein angiography were evaluated. RESULTS: The mean age of the patients was 68.1±5.7 (range: 63–82) years, the mean follow-up was 19.9±14.5 (range: 12–67) months, and the mean number of injections was 4.0±1.4 (range: 3–15). The initial VA was 39.3±17.9 (range: 1–65) letters, CMT was 272.7±104 (range: 164–587) μm, and the initial lesion width was 11.4±10.5 (range: 1.3–45.7) mm(2). The VA was 41.4±20.1 (range: 5–75) and 36.9±21.8 (range: 4–80) letters (p=0.150), CMT was 270.7±110 (range: 159–570) and 230.4±108 (range: 109–667) μm (p=0.009) and the lesion width was 10.9±11.5 (range: 1.1–39.7) and 10.4±11.6 (range: 1.2–44.3) mm(2) at 6(th) and 12(th) month, respectively. No factor was found to be associated with final CMT. CONCLUSION: Although the final visual outcome is limited by the progression of the disease, hemorrhagic lesions treated with ranibizumab have stable anatomical outcome. Health Directorate of Istanbul 2022-03-23 /pmc/articles/PMC9039638/ /pubmed/35582510 http://dx.doi.org/10.14744/nci.2021.52323 Text en Copyright © 2022 by Istanbul Provincial Directorate of Health - Available online at www.northclinist.com https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. |
spellingShingle | Original Article - Ophthalmology Dikmetas, Ozlem Kadayifcilar, Sibel Eldem, Bora Feyzullayeva, Ulkar Ranibizumab therapy for predominantly hemorrhagic neovascular age-related macular degeneration |
title | Ranibizumab therapy for predominantly hemorrhagic neovascular age-related macular degeneration |
title_full | Ranibizumab therapy for predominantly hemorrhagic neovascular age-related macular degeneration |
title_fullStr | Ranibizumab therapy for predominantly hemorrhagic neovascular age-related macular degeneration |
title_full_unstemmed | Ranibizumab therapy for predominantly hemorrhagic neovascular age-related macular degeneration |
title_short | Ranibizumab therapy for predominantly hemorrhagic neovascular age-related macular degeneration |
title_sort | ranibizumab therapy for predominantly hemorrhagic neovascular age-related macular degeneration |
topic | Original Article - Ophthalmology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039638/ https://www.ncbi.nlm.nih.gov/pubmed/35582510 http://dx.doi.org/10.14744/nci.2021.52323 |
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