Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107513
DC FieldValueLanguage
dc.contributor.authorProvidência, Joana-
dc.contributor.authorRodrigues, Tiago M-
dc.contributor.authorOliveira, Mariana-
dc.contributor.authorBernardes, João-
dc.contributor.authorMarques, João Pedro-
dc.contributor.authorMurta, Joaquim N.-
dc.contributor.authorSilva, Rufino-
dc.date.accessioned2023-07-18T09:19:08Z-
dc.date.available2023-07-18T09:19:08Z-
dc.date.issued2018-
dc.identifier.issn2314-6133pt
dc.identifier.issn2314-6141pt
dc.identifier.urihttps://hdl.handle.net/10316/107513-
dc.description.abstractIntravitreal injections of antivascular endothelial growth factors have been considered a milestone in the treatment of neovascular age-related macular degeneration (nAMD). However, the increasing incidence of AMD and the burden of visits and injections overcharge both the patient and the healthcare systems. Real-world solutions depend on treatment protocols aimed at optimizing the number of clinical visits while guaranteeing good functional outcomes. We performed a retrospective analysis of 72 eyes from 63 naïve patients diagnosed with nAMD that underwent a fixed intravitreal protocol consisting of bimonthly injections after a three-month loading dose, with either Aflibercept or Ranibizumab (no predefined criteria for treatment selection). Best corrected visual acuity (BCVA) and optical coherence tomography were analyzed at baseline and during follow-up clinical visits (months 3, 6, 12, and 18). From the included participants, 42 followed a fixed regimen with Aflibercept and 30 with Ranibizumab. At the 12-month visit, there was not a statistically significant difference in the mean change of BCVA between the two groups (p=0.121); however, the mean difference in the central retinal thickness was significantly superior in the Aflibercept group (-142.2 versus -51.5, p=0.011). The described fixed regimen seems to be efficient in the treatment of nAMD in a clinical practice setting.pt
dc.language.isoengpt
dc.publisherHindawipt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshAgedpt
dc.subject.meshAged, 80 and overpt
dc.subject.meshAngiogenesis Inhibitorspt
dc.subject.meshFemalept
dc.subject.meshFollow-Up Studiespt
dc.subject.meshHumanspt
dc.subject.meshIntravitreal Injectionspt
dc.subject.meshMacular Degenerationpt
dc.subject.meshMalept
dc.subject.meshRanibizumabpt
dc.subject.meshReceptors, Vascular Endothelial Growth Factorpt
dc.subject.meshRecombinant Fusion Proteinspt
dc.subject.meshRetrospective Studiespt
dc.subject.meshTomography, Optical Coherencept
dc.subject.meshTreatment Outcomept
dc.subject.meshVisual Acuitypt
dc.titleReal-World Results of Aflibercept versus Ranibizumab for the Treatment of Exudative AMD Using a Fixed Regimenpt
dc.typearticle-
degois.publication.firstPage9276580pt
degois.publication.lastPage7pt
degois.publication.titleBioMed Research Internationalpt
dc.peerreviewedyespt
dc.identifier.doi10.1155/2018/9276580pt
degois.publication.volume2018pt
dc.date.embargo2018-01-01*
uc.date.periodoEmbargo0pt
item.languageiso639-1en-
item.openairetypearticle-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-1014-0483-
crisitem.author.orcid0000-0001-8926-5176-
crisitem.author.orcid0000-0001-8676-0833-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
I&D IBILI - Artigos em Revistas Internacionais
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This item is licensed under a Creative Commons License Creative Commons