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ANTI-VEGF therapies in neovascular age-related macular degeneration: a scoping review of functional and morphological outcomes in older adults

dc.contributor.authorQueirós, Marta
dc.contributor.authorTeixeira, Daniela
dc.contributor.authorJesus, Ângelo
dc.contributor.authorSantos, Marlene
dc.contributor.authorMoreira, Fernando
dc.contributor.authorFernandes, Sara R.
dc.contributor.authorSantos, Marlene
dc.contributor.authorMoreira, Fernando
dc.contributor.authorFernandes, Sara
dc.date.accessioned2026-09-16T09:31:56Z
dc.date.available2026-09-16T09:31:56Z
dc.date.issued2025-10
dc.description.abstractAge-related macular degeneration (AMD) is one of the leading causes of blindness in individuals over 60 years of age and is classified into two main subtypes: geographic atrophy (dry AMD) and neovascular AMD (wet AMD). Antivascular endothelial growth factor (anti-VEGF) agents are the standard treatment for neovascular AMD, although guidelines diverge regarding first-line choices. This scoping review aims to identify and characterize current scientific evidence on the use of anti-VEGF agents in the treatment of neovascular AMD. A systematic search was conducted in PubMed for observational or experimental studies published between 2020 and April 2025. Eligible studies included individuals aged ⩾60 years, reported on the use of anti-VEGF therapy for neovascular AMD, and assessed both functional (visual acuity) and morphological outcomes. Sixty-five studies met the inclusion criteria – 56 observational studies (prospective cohorts and cross-sectional designs), and nine clinical trials. Aflibercept (34%), faricimab (18%), and ranibizumab (15%) were the most commonly agents. Ranibizumab and aflibercept consistently improved visual acuity, with average gains of 7–15 ETDRS letters. Bevacizumab yielded more variable outcomes. In refractory patients, brolucizumab or faricimab showed anatomical improvements; however, brolucizumab was associated to higher risk of intraocular inflammation. The findings suggest that clinical and anatomical factors, such as persistent subretinal fluid, central retinal thickness, and initial treatment response, may help guide a more individualised selection of anti-VEGF. While ranibizumab and aflibercept remain well-established options, faricimab shows potential, in patients with suboptimal response to conventional agents.eng
dc.identifier.citationQueirós, M., Teixeira, D., Jesus, Â., Santos, M., Moreira, F., & Fernandes, S. R. (2025). ANTI-VEGF therapies in neovascular age-related macular degeneration: A scoping review of functional and morphological outcomes in older adults. 13th APLF Annual Conference, TherapeuTic advances in drug safety 16(S1), 47–48. https://journals.sagepub.com/doi/epub/10.1177/20420986251379201
dc.identifier.doi10.1177/20420986251379201
dc.identifier.eissn2042-0994
dc.identifier.issn2042-0986
dc.identifier.urihttp://hdl.handle.net/10400.22/32715
dc.language.isoeng
dc.peerreviewedyes
dc.publisherSAGE Publications
dc.relation.hasversionhttps://journals.sagepub.com/doi/10.1177/20420986251379201
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectAnti-VEGF
dc.subjectNeovascular age-related macular degeneration
dc.subjectVisual acuity outcomes
dc.titleANTI-VEGF therapies in neovascular age-related macular degeneration: a scoping review of functional and morphological outcomes in older adultseng
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferenceDate2025-10
oaire.citation.conferencePlaceAveiro
oaire.citation.endPage48
oaire.citation.issueS1
oaire.citation.startPage47
oaire.citation.title13th APLF Annual Conference - TherapeuTic advances in drug safety
oaire.citation.volume16
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85
person.familyNameSantos
person.familyNameMoreira
person.familyNameFernandes
person.givenNameMarlene
person.givenNameFernando
person.givenNameSara
person.identifier1508370
person.identifier2947760
person.identifier.ciencia-id8311-B967-31C4
person.identifier.ciencia-id5F16-AB92-94D0
person.identifier.ciencia-id1C12-D800-38A4
person.identifier.orcid0000-0001-5020-5942
person.identifier.orcid0000-0002-3452-1459
person.identifier.orcid0000-0001-7042-1941
person.identifier.scopus-author-id57110502000
person.identifier.scopus-author-id57203278917
relation.isAuthorOfPublication8ce9ee39-a4c6-46ae-99e2-49397b550f1b
relation.isAuthorOfPublication81213e80-09a5-4655-93dc-e54199edb2fe
relation.isAuthorOfPublication6c2ed5f0-c3fd-4559-99a3-b8d78d019b47
relation.isAuthorOfPublication.latestForDiscovery8ce9ee39-a4c6-46ae-99e2-49397b550f1b

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