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Successful optimization of adalimumab therapy in refractory uveitis due to Behçet´s disease

dc.contributor.authorMartín Varillas, José Luis
dc.contributor.authorDíaz Valle, David
dc.contributor.authorPato, Esperanza
dc.contributor.authorBlanco, Ricardo
dc.date.accessioned2024-12-03T09:37:15Z
dc.date.available2024-12-03T09:37:15Z
dc.date.issued2018-09-15
dc.description.abstractPurpose: To assess efficacy, safety, and cost-effectiveness of adalimumab (ADA) therapy optimization in a large series of patients with uveitis due to Behçet disease (BD) who achieved remission after the use of this biologic agent. Design: Open-label multicenter study of ADA-treated patients with BD uveitis refractory to conventional immunosuppressants. Subjects: Sixty-five of 74 patients with uveitis due to BD, who achieved remission after a median ADA duration of 6 (range, 3–12) months. ADA was optimized in 23 (35.4%) of them. This biologic agent was maintained at a dose of 40 mg/subcutaneously/2 weeks in the remaining 42 patients. Methods: After remission, based on a shared decision between the patient and the treating physician, ADA was optimized. When agreement between patient and physician was reached, optimization was performed by prolonging the ADA dosing interval progressively. Comparison between optimized and nonoptimized patients was performed. Main Outcome Measures: Efficacy, safety, and cost-effectiveness in optimized and nonoptimized groups. To determine efficacy, intraocular inflammation (anterior chamber cells, vitritis, and retinal vasculitis), macular thickness, visual acuity, and the sparing effect of glucocorticoids were assessed. Results: No demographic or ocular differences were found at the time of ADA onset between the optimized and the nonoptimized groups. Most ocular outcomes were similar after a mean ± standard deviation follow-up of 34.7±13.3 and 26±21.3 months in the optimized and nonoptimized groups, respectively. However, relevant adverse effects were only seen in the nonoptimized group (lymphoma, pneumonia, severe local reaction at the injection site, and bacteremia by Escherichia coli, 1 each). Moreover, the mean ADA treatment costs were lower in the optimized group than in the nonoptimized group (6101.25 euros/patient/year vs. 12 339.48; P < 0.01). Conclusion: ADA optimization in BD uveitis refractory to conventional therapy is effective, safe, and cost-effective.
dc.description.departmentDepto. de Inmunología, Oftalmología y ORL
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationMartín-Varillas, J. L., Calvo-Río, V., Beltrán, E., Sánchez-Bursón, J., Mesquida, M., Adán, A., Hernandez, M. V., Garfella, M. H., Pascual, E. V., Martínez-Costa, L., Sellas-Fernández, A., Cordero-Coma, M., Díaz-Llopis, M., Gallego, R., Salom, D., Ortego, N., García-Serrano, J. L., Callejas-Rubio, J. L., Herreras, J. M., García-Aparicio, Á., … Blanco, R. (2018). Successful Optimization of Adalimumab Therapy in Refractory Uveitis Due to Behçet's Disease. Ophthalmology, 125(9), 1444–1451. https://doi.org/10.1016/j.ophtha.2018.02.020
dc.identifier.doi10.1016/j.ophtha.2018.02.020
dc.identifier.issn0161-6420
dc.identifier.officialurlhttps://doi.org/10.1016/j.ophtha.2018.02.020
dc.identifier.relatedurlhttps://www.sciencedirect.com/science/article/abs/pii/S0161642017333900
dc.identifier.urihttps://hdl.handle.net/20.500.14352/111932
dc.issue.number9
dc.journal.titleOphthalmology
dc.language.isoeng
dc.page.final1451
dc.page.initial1444
dc.publisherElsevier
dc.rights.accessRightsrestricted access
dc.subject.cdu612.017
dc.subject.ucmCiencias Biomédicas
dc.subject.unesco32 Ciencias Médicas
dc.titleSuccessful optimization of adalimumab therapy in refractory uveitis due to Behçet´s disease
dc.typejournal article
dc.type.hasVersionCVoR
dc.volume.number125
dspace.entity.typePublication
relation.isAuthorOfPublication3e2b98e5-5c02-400b-8823-90887624c010
relation.isAuthorOfPublication.latestForDiscovery3e2b98e5-5c02-400b-8823-90887624c010

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