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dc.contributor.authorBarroso-García, Nuria
dc.contributor.authorMartín Varillas, José Luis
dc.contributor.authorSánchez Bilbao, Lara
dc.contributor.authorMartín-Gutiérrez, Adrián
dc.contributor.authorAdan, Alfredo M.
dc.contributor.authorHernanz-Rodríguez, Inés
dc.contributor.authorBeltrán-Catalán, Emma
dc.contributor.authorCordero-Coma, Miguel
dc.contributor.authorDíaz-Valle, David
dc.contributor.authorHernández-Garfella, Marisa
dc.contributor.authorMartínez-Costa, Lucía
dc.contributor.authorDíaz-Llopis, Manuel
dc.contributor.authorHerreras, José M.
dc.contributor.authorMaíz-Aonso, Olga
dc.contributor.authorTorre-Salaberri, Ignacio
dc.contributor.authorCalvo del Río, Vanesa
dc.contributor.authorDemetrio Pablo, Rosalía
dc.contributor.authorHernández Hernández, José Luis 
dc.contributor.authorBlanco Alonso, Ricardo 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-04-11T14:13:58Z
dc.date.available2025-04-11T14:13:58Z
dc.date.issued2024
dc.identifier.issn2077-0383
dc.identifier.urihttps://hdl.handle.net/10902/36251
dc.description.abstractBackground: The leading cause of blindness due to non-infectious uveitis is cystoid macular edema (CME). Behçet's disease (BD) is one of the most commonly conditions related to CME. Objectives: To compare the effectiveness and safety of adalimumab (ADA), infliximab (IFX) and certolizumab (CZP) in refractory CME due to BD. Methods: Multicenter study of BD-CME patients with no response to glucocorticoids (GCs) and at least one conventional immunosuppressive drug. At baseline, all patients presented CME, defined by OCT > 300 µ. The effectiveness of ADA, IFX and CZP was assessed over a 2-year period from baseline using the following ocular parameters: macular thickness (µm), visual acuity (BCVA), anterior chamber (AC) cells and vitritis. Mixed-effects regression models were applied. Results: a total of 50 patients (75 eyes) were studied (ADA = 25; IFX = 15 and CZP = 10). No significant differences in demographic parameters were found among the three groups. However, individuals in the CZP group had a significantly extended time from diagnosis to treatment onset (72 (36-120) months, p = 0.03) and had received a higher number of biological therapies (1.7 ± 1.1) compared to the ADA and IFX groups. Within the CZP group, ADA and IFX were previously administrated in seven patients. After 2 years of follow-up, a rapid and sustained reduction in macular thickness was noted in all three groups with no significant differences between them. Additionally, enhancements in BCVA, AC cells and vitritis were also observed. No serious adverse events were reported in the CZP group, although one isolated case of bacteremia was documented in the ADA group. ADA, IFX and CZP appear to be effective and safe treatments for refractory CME in BD. CZP seems to remain effective even in patients with an insufficient response to ADA and/or IFX. Conclusions: ADA, IFX and CZP appear to be effective and safe treatments for refractory CME in BD. CZP seems to remain effective even in patients with an insufficient response to ADA and/or IFX.es_ES
dc.description.sponsorshipFunding: This research received no external funding.es_ES
dc.format.extent12 p.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rights© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.es_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceJournal of Clinical Medicine, 2024, 13(23), 7388es_ES
dc.subject.otherUveitises_ES
dc.subject.otherCystoid macular edemaes_ES
dc.subject.otherBehçet diseasees_ES
dc.subject.otherTNF inhibitor monoclonal antibodieses_ES
dc.subject.otherAdalimumabes_ES
dc.subject.otherInfliximabes_ES
dc.subject.otherCertolizumab pegoles_ES
dc.titleComparative study of adalimumab, infliximab and certolizumab pegol in the treatment of cystoid macular edema due to Behçet's diseasees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.3390/jcm13237388es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/jcm13237388
dc.type.versionpublishedVersiones_ES


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© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.Excepto si se señala otra cosa, la licencia del ítem se describe como © 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.