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Efficacy and safety of Pro Re Nata regimen without loading dose ranibizumab injections in retinal vein occlusion
OBJECTIVES: To evaluate the effects and safety of intravitreal ranibizumab on visual acuity and anatomic results in the treatment of macular edema due to retinal vein occlusion (RVO). METHODS: Forty Six eyes of 45 patients who were administered intravitreal ranibizumab because of macular edema due t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Professional Medical Publications
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485261/ https://www.ncbi.nlm.nih.gov/pubmed/26150834 http://dx.doi.org/10.12669/pjms.313.7218 |
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author | Unsal, Erkan Eltutar, Kadir Sultan, Pınar Gungel, Hulya |
author_facet | Unsal, Erkan Eltutar, Kadir Sultan, Pınar Gungel, Hulya |
author_sort | Unsal, Erkan |
collection | PubMed |
description | OBJECTIVES: To evaluate the effects and safety of intravitreal ranibizumab on visual acuity and anatomic results in the treatment of macular edema due to retinal vein occlusion (RVO). METHODS: Forty Six eyes of 45 patients who were administered intravitreal ranibizumab because of macular edema due to Retinal Vein Occlusion (RVO) were included in this retrospective clinical study. During monthly follow-up, the best corrected visual acuity values in terms of LogMAR with The Early Treatment Diabetic Retinopathy Study (ETDRS) chart, central macular thickness (CMT), and complications were examined. Cases were classified as central retinal vein occlusion (CRVO), superotemporal branch retinal vein occlusion (BRVO), and inferotemporal BRVO. We only included RVO patients but using ETDRS chart for the vision measurement. RESULTS: In all follow-up months, there was a significant increase in BCVA in all RVO cases and in superotemporal BRVO cases after the first injection of ranibizumab. Although there was no significant increase in the 1(st) month of follow-up period compared to pre-treatment, there was significant increase in 2-6 months in inferotemporal BRVO patients. There was no statistically significant increase in 1(st) and 2(nd) month follow-up periods compared to pre-treatment; however there was a significant increase in 3-6 months in the CRVO patients. There was a significant decrease in average CMT measurements in all follow-up months compared to pre-treatment in all RVO cases, in superotemporal and inferotemporal BRVO cases. There was no significant decrease in average CMT measurements in the 1(st), 2nd, and 3(rd) months compared to pre-treatment although there was a significant decrease in 4-6 months in cases included in the CRVO patients. CONCLUSIONS: Intraocular ranibizumab injections provided rapid, effective treatment for macular edema due to RVO with low rates of ocular and nonocular safety events. However, repeated injections and frequent follow-up intervals may be required. |
format | Online Article Text |
id | pubmed-4485261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Professional Medical Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-44852612015-07-06 Efficacy and safety of Pro Re Nata regimen without loading dose ranibizumab injections in retinal vein occlusion Unsal, Erkan Eltutar, Kadir Sultan, Pınar Gungel, Hulya Pak J Med Sci Original Article OBJECTIVES: To evaluate the effects and safety of intravitreal ranibizumab on visual acuity and anatomic results in the treatment of macular edema due to retinal vein occlusion (RVO). METHODS: Forty Six eyes of 45 patients who were administered intravitreal ranibizumab because of macular edema due to Retinal Vein Occlusion (RVO) were included in this retrospective clinical study. During monthly follow-up, the best corrected visual acuity values in terms of LogMAR with The Early Treatment Diabetic Retinopathy Study (ETDRS) chart, central macular thickness (CMT), and complications were examined. Cases were classified as central retinal vein occlusion (CRVO), superotemporal branch retinal vein occlusion (BRVO), and inferotemporal BRVO. We only included RVO patients but using ETDRS chart for the vision measurement. RESULTS: In all follow-up months, there was a significant increase in BCVA in all RVO cases and in superotemporal BRVO cases after the first injection of ranibizumab. Although there was no significant increase in the 1(st) month of follow-up period compared to pre-treatment, there was significant increase in 2-6 months in inferotemporal BRVO patients. There was no statistically significant increase in 1(st) and 2(nd) month follow-up periods compared to pre-treatment; however there was a significant increase in 3-6 months in the CRVO patients. There was a significant decrease in average CMT measurements in all follow-up months compared to pre-treatment in all RVO cases, in superotemporal and inferotemporal BRVO cases. There was no significant decrease in average CMT measurements in the 1(st), 2nd, and 3(rd) months compared to pre-treatment although there was a significant decrease in 4-6 months in cases included in the CRVO patients. CONCLUSIONS: Intraocular ranibizumab injections provided rapid, effective treatment for macular edema due to RVO with low rates of ocular and nonocular safety events. However, repeated injections and frequent follow-up intervals may be required. Professional Medical Publications 2015 /pmc/articles/PMC4485261/ /pubmed/26150834 http://dx.doi.org/10.12669/pjms.313.7218 Text en Copyright: © Pakistan Journal of Medical Sciences http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Unsal, Erkan Eltutar, Kadir Sultan, Pınar Gungel, Hulya Efficacy and safety of Pro Re Nata regimen without loading dose ranibizumab injections in retinal vein occlusion |
title | Efficacy and safety of Pro Re Nata regimen without loading dose ranibizumab injections in retinal vein occlusion |
title_full | Efficacy and safety of Pro Re Nata regimen without loading dose ranibizumab injections in retinal vein occlusion |
title_fullStr | Efficacy and safety of Pro Re Nata regimen without loading dose ranibizumab injections in retinal vein occlusion |
title_full_unstemmed | Efficacy and safety of Pro Re Nata regimen without loading dose ranibizumab injections in retinal vein occlusion |
title_short | Efficacy and safety of Pro Re Nata regimen without loading dose ranibizumab injections in retinal vein occlusion |
title_sort | efficacy and safety of pro re nata regimen without loading dose ranibizumab injections in retinal vein occlusion |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485261/ https://www.ncbi.nlm.nih.gov/pubmed/26150834 http://dx.doi.org/10.12669/pjms.313.7218 |
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