Amb motiu del tancament d'estiu, la validació de documents es reprendrà a partir del 28 d'agost de 2026. Disculpeu les molèsties.
Con motivo del cierre de verano, la validación de documentos se reanudará a partir del 28 de agosto de 2026. Disculpad las molestias
Due to the summer closure, document validation will resume starting August 28, 2026. We apologize for any inconvenience.

Golimumab as rescue therapy for refractory immune-mediated uveitis: a three-center experience

dc.contributor.authorCordero Coma, Miguel
dc.contributor.authorCalvo Río, Vanesa
dc.contributor.authorAdán Civera, Alfredo
dc.contributor.authorBlanco, Ricardo
dc.contributor.authorÁlvarez Castro, Carolina
dc.contributor.authorMesquida, Marina
dc.contributor.authorCalleja, Sara
dc.contributor.authorGonzález-Gay, Miguel A.
dc.contributor.authorRuíz de Morales, José G.
dc.date.accessioned2017-07-04T13:43:47Z
dc.date.available2017-07-04T13:43:47Z
dc.date.issued2014-05-28
dc.date.updated2017-07-04T13:43:47Z
dc.description.abstractObjective. To evaluate, in three Spanish tertiary referral centres, the short-term safety and efficacy of golimumab (GLM) for treatment of immune-mediated uveitis resistant to previous immunosuppressive therapy. Methods. Nonrandomized retrospective interventional case series. Thirteen patients with different types of uveitis that were resistant to treatment with at least 2 previous immunosuppressors were included in this study. All included patients were treated with GLM (50 mg every four weeks) during at least 6 months. Clinical evaluation and treatment-related side effects were assessed at least four times in all included patients. Results. Eight men and 5 women (22 affected eyes) with a median age of 30 years (range 20-38) and active immune-mediated uveitides were studied. GLM was used in combination with conventional immunosuppressors in 7 patients (53.8%). GLM therapy achieved complete control of inflammation in 12/13 patients (92.3%) after six months of treatment. There was a statistically significant improvement in mean BCVA (0.60 versus 0.68, P - 0.009) and mean 1 mm central retinal thickness (317 versus 261.2 mu, P -0.05) at the six-month endpoint when compared to basal values. No major systemic adverse effects associated with GLM therapy were observed. Conclusions. GLM is a new and promising therapeutic option for patients with severe and refractory uveitis.
dc.format.extent6 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec666315
dc.identifier.issn0962-9351
dc.identifier.pmid24976689
dc.identifier.urihttps://hdl.handle.net/2445/113335
dc.language.isoeng
dc.publisherHindawi Publishing Corporation
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1155/2014/717598
dc.relation.ispartofMediators of Inflammation, 2014, vol. 2014
dc.relation.urihttps://doi.org/10.1155/2014/717598
dc.rightscc-by (c) Cordero Coma, Miguel et al., 2014
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)
dc.subject.classificationUveïtis
dc.subject.classificationOftalmologia
dc.subject.otherUveitis
dc.subject.otherOphthalmology
dc.titleGolimumab as rescue therapy for refractory immune-mediated uveitis: a three-center experience
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

Fitxers

Paquet original

Mostrant 1 - 1 de 1
Carregant...
Miniatura
Nom:
666315.pdf
Mida:
1.25 MB
Format:
Adobe Portable Document Format