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Faricimab for Treatment-Resistant Diabetic Macular Edema
PURPOSE: To assess the short-term outcomes in treatment-resistant diabetic macular edema (DME) patients changed from intravitreal aflibercept (IVA) to intravitreal faricimab (IVF). METHODS: A retrospective review was undertaken on DME subjects receiving IVA therapy at a single private practice. Pati...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420435/ https://www.ncbi.nlm.nih.gov/pubmed/36042912 http://dx.doi.org/10.2147/OPTH.S381503 |
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author | Rush, Ryan B Rush, Sloan W |
author_facet | Rush, Ryan B Rush, Sloan W |
author_sort | Rush, Ryan B |
collection | PubMed |
description | PURPOSE: To assess the short-term outcomes in treatment-resistant diabetic macular edema (DME) patients changed from intravitreal aflibercept (IVA) to intravitreal faricimab (IVF). METHODS: A retrospective review was undertaken on DME subjects receiving IVA therapy at a single private practice. Patients were separated into study and control cohorts. Both study and control patients had received more than or equal to six IVA injections during the preceding 12 months, more than or equal to four IVA injections during the preceding 6 months, had a central macular thickness (CMT) on optical coherence tomography (OCT) of ≥300 µm, and had retinal fluid on OCT before cohort assignment. Study patients were switched to IVF and underwent three injections within 4 months, whereas control patients stayed on IVA during the same period and received three injections within 4 months. RESULTS: There were 51 patients analyzed. There were 37.5% (9/24) in the study group and 3.7% (1/27) in the control group who achieved a CMT of less than 300 µm without retinal fluid on OCT at the end of the 4-month study (p=0.001). There were 41.7% (10/24) in the study group and 11.1% (3/27) in the control group who had gained two or more lines of visual acuity at the end of the 4-month study (p=0.01). CONCLUSION: For a significant minority, IVF can improve the short-term visual and anatomic outcomes in treatment-resistant DME patients formerly managed with IVA. Longer follow-up is needed to determine if such improvements can be preserved. |
format | Online Article Text |
id | pubmed-9420435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-94204352022-08-29 Faricimab for Treatment-Resistant Diabetic Macular Edema Rush, Ryan B Rush, Sloan W Clin Ophthalmol Original Research PURPOSE: To assess the short-term outcomes in treatment-resistant diabetic macular edema (DME) patients changed from intravitreal aflibercept (IVA) to intravitreal faricimab (IVF). METHODS: A retrospective review was undertaken on DME subjects receiving IVA therapy at a single private practice. Patients were separated into study and control cohorts. Both study and control patients had received more than or equal to six IVA injections during the preceding 12 months, more than or equal to four IVA injections during the preceding 6 months, had a central macular thickness (CMT) on optical coherence tomography (OCT) of ≥300 µm, and had retinal fluid on OCT before cohort assignment. Study patients were switched to IVF and underwent three injections within 4 months, whereas control patients stayed on IVA during the same period and received three injections within 4 months. RESULTS: There were 51 patients analyzed. There were 37.5% (9/24) in the study group and 3.7% (1/27) in the control group who achieved a CMT of less than 300 µm without retinal fluid on OCT at the end of the 4-month study (p=0.001). There were 41.7% (10/24) in the study group and 11.1% (3/27) in the control group who had gained two or more lines of visual acuity at the end of the 4-month study (p=0.01). CONCLUSION: For a significant minority, IVF can improve the short-term visual and anatomic outcomes in treatment-resistant DME patients formerly managed with IVA. Longer follow-up is needed to determine if such improvements can be preserved. Dove 2022-08-24 /pmc/articles/PMC9420435/ /pubmed/36042912 http://dx.doi.org/10.2147/OPTH.S381503 Text en © 2022 Rush and Rush. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Rush, Ryan B Rush, Sloan W Faricimab for Treatment-Resistant Diabetic Macular Edema |
title | Faricimab for Treatment-Resistant Diabetic Macular Edema |
title_full | Faricimab for Treatment-Resistant Diabetic Macular Edema |
title_fullStr | Faricimab for Treatment-Resistant Diabetic Macular Edema |
title_full_unstemmed | Faricimab for Treatment-Resistant Diabetic Macular Edema |
title_short | Faricimab for Treatment-Resistant Diabetic Macular Edema |
title_sort | faricimab for treatment-resistant diabetic macular edema |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420435/ https://www.ncbi.nlm.nih.gov/pubmed/36042912 http://dx.doi.org/10.2147/OPTH.S381503 |
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