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Long-term outcomes of intravenous fibrinolysis in central retinal artery occlusion
Central retinal artery occlusion (CRAO) is an ophthalmologic emergency that can lead to irreversible loss of vision. Intravenous thrombolysis (IVT) has been used experimentally for its treatment. Our study aimed to evaluate the effect of emergency IVT on CRAO and its impact on visual acuity outcomes...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665428/ https://www.ncbi.nlm.nih.gov/pubmed/37993533 http://dx.doi.org/10.1038/s41598-023-47987-9 |
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author | Kozner, Pavel Eichenmann, Libor Ceska Burdova, Marie Pavlikova, Marketa Hlozanek, Martin Dotrelova, Dagmar |
author_facet | Kozner, Pavel Eichenmann, Libor Ceska Burdova, Marie Pavlikova, Marketa Hlozanek, Martin Dotrelova, Dagmar |
author_sort | Kozner, Pavel |
collection | PubMed |
description | Central retinal artery occlusion (CRAO) is an ophthalmologic emergency that can lead to irreversible loss of vision. Intravenous thrombolysis (IVT) has been used experimentally for its treatment. Our study aimed to evaluate the effect of emergency IVT on CRAO and its impact on visual acuity outcomes. We conducted a retrospective observational study of patients with CRAO. A total of 46 patients with CRAO were analysed; 16 patients received IVT treatment (IVT group) while 30 did not (no-IVT group). Seven patients from the IVT group received IVT early, within 4.5 hours (h) after the onset of symptoms (early-IVT), and 9 patients received it beyond this timeframe (late-IVT). The median time-to-hospital was 8.5 h: 3 h for the IVT group and 24 h for the no-IVT group. The median time-to-treatment was 5 h. The median outcome of visual acuity was 0.05 in the early-IVT, 0.025 in the late-IVT, and 0.01 in the no-IVT group. Among patients who received IVT early, 86% exhibited significant visual improvement. This improvement was four-fold greater compared to all other groups (p = 0.040), including the late-IVT (p = 0.011) and no-IVT groups (p = 0.023). No complications of the treatment were reported. Our study confirms that the administration of IVT treatment for CRAO within the 4.5-h time window is both safe and effective. |
format | Online Article Text |
id | pubmed-10665428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106654282023-11-22 Long-term outcomes of intravenous fibrinolysis in central retinal artery occlusion Kozner, Pavel Eichenmann, Libor Ceska Burdova, Marie Pavlikova, Marketa Hlozanek, Martin Dotrelova, Dagmar Sci Rep Article Central retinal artery occlusion (CRAO) is an ophthalmologic emergency that can lead to irreversible loss of vision. Intravenous thrombolysis (IVT) has been used experimentally for its treatment. Our study aimed to evaluate the effect of emergency IVT on CRAO and its impact on visual acuity outcomes. We conducted a retrospective observational study of patients with CRAO. A total of 46 patients with CRAO were analysed; 16 patients received IVT treatment (IVT group) while 30 did not (no-IVT group). Seven patients from the IVT group received IVT early, within 4.5 hours (h) after the onset of symptoms (early-IVT), and 9 patients received it beyond this timeframe (late-IVT). The median time-to-hospital was 8.5 h: 3 h for the IVT group and 24 h for the no-IVT group. The median time-to-treatment was 5 h. The median outcome of visual acuity was 0.05 in the early-IVT, 0.025 in the late-IVT, and 0.01 in the no-IVT group. Among patients who received IVT early, 86% exhibited significant visual improvement. This improvement was four-fold greater compared to all other groups (p = 0.040), including the late-IVT (p = 0.011) and no-IVT groups (p = 0.023). No complications of the treatment were reported. Our study confirms that the administration of IVT treatment for CRAO within the 4.5-h time window is both safe and effective. Nature Publishing Group UK 2023-11-22 /pmc/articles/PMC10665428/ /pubmed/37993533 http://dx.doi.org/10.1038/s41598-023-47987-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kozner, Pavel Eichenmann, Libor Ceska Burdova, Marie Pavlikova, Marketa Hlozanek, Martin Dotrelova, Dagmar Long-term outcomes of intravenous fibrinolysis in central retinal artery occlusion |
title | Long-term outcomes of intravenous fibrinolysis in central retinal artery occlusion |
title_full | Long-term outcomes of intravenous fibrinolysis in central retinal artery occlusion |
title_fullStr | Long-term outcomes of intravenous fibrinolysis in central retinal artery occlusion |
title_full_unstemmed | Long-term outcomes of intravenous fibrinolysis in central retinal artery occlusion |
title_short | Long-term outcomes of intravenous fibrinolysis in central retinal artery occlusion |
title_sort | long-term outcomes of intravenous fibrinolysis in central retinal artery occlusion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665428/ https://www.ncbi.nlm.nih.gov/pubmed/37993533 http://dx.doi.org/10.1038/s41598-023-47987-9 |
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