Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/216867
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dc.contributor.authorRaad, Fatima-
dc.contributor.authorLuque, Paula-
dc.contributor.authorGarcia Ledo, Sofia-
dc.contributor.authorAlda Lozano, Alicia-
dc.contributor.authorLlorens Bellés, Víctor-
dc.contributor.authorEspejo, Antonio-
dc.contributor.authorHeras, Henar-
dc.contributor.authorSantana, Lucia-
dc.contributor.authorTrapiella, Luis-
dc.contributor.authorFanlo, Patricia-
dc.contributor.authorAdán Civera, Alfredo-
dc.contributor.authorEspinosa Garriga, Gerard-
dc.contributor.authorNavarrete, Nuria-
dc.date.accessioned2024-12-02T13:13:16Z-
dc.date.available2025-05-01T05:10:09Z-
dc.date.issued2024-05-01-
dc.identifier.issn0927-3948-
dc.identifier.urihttps://hdl.handle.net/2445/216867-
dc.description.abstractObjectiveTo describe the efficacy and safety of adalimumab for the treatment of non-infectious uveitis (NIU) in four Uveitis Units from tertiary Spanish hospitals. MethodsMulticenter and retrospective clinical cohort study including all patients with NIU treated with adalimumab from January 2012 to October 2022 in four uveitis units was performed. Efficacy was measured with the number of relapses, ocular inflammation and reduction in immunosuppression and corticosteroid dosage before and after adalimumab use. We collected data regarding adverse effects and examined the immunogenicity of adalimumab. ResultsOne hundred and twenty-two patients (59% females), with a mean age of 48.6 years (SD = 14.8) accounting for 217 eyes were included. The majority (92.6%) were Caucasian. Uveitis analyzed were predominantly panuveitis (34.7%), bilateral (77.9%), acute (41.5%), and non-granulomatous (90%). Most of them were immune mediated (42.6%), and the main reason to initiate adalimumab was refractory disease (96.7%). The analysis was statistically significant due to the reduction in the number of immunosuppressive drugs as well as the dose of oral corticosteroids and the number of relapses during follow-up (p < 0.001). The decrease in ocular inflammation parameters and the improvement in visual acuity (p < 0.05) were also significant. There were no deaths due to the drug and only one reported case of serious infection. In total, 10.9% of 73 patients tested developed anti-adalimumab antibodies and 4.1% lupus-like. ConclusionsWe consider adalimumab as a leading drug in the treatment of NIU with high safety and efficacy.ca
dc.format.extent23 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoengca
dc.publisherTaylor and Francisca
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1080/09273948.2024.2344712-
dc.relation.ispartofOcular Immunology And Inflammation, 2024, p.1-7-
dc.relation.urihttps://doi.org/10.1080/09273948.2024.2344712-
dc.rights(c) Taylor and Francis, 2024-
dc.sourceArticles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)-
dc.subject.classificationUveïtis-
dc.subject.classificationAnticossos monoclonals-
dc.subject.classificationTerapèutica-
dc.subject.otherUveitis-
dc.subject.otherMonoclonal antibodies-
dc.subject.otherTherapeutics-
dc.titleAdalimumab for the Treatment of Non-Infectious Uveitis: A Real Life Experienceca
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.date.updated2024-11-27T12:03:56Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.idimarina9425833-
dc.identifier.pmid38691840-
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

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