Utilize este identificador para referenciar este registo: http://hdl.handle.net/10451/46594
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degois.publication.firstPage195pt_PT
degois.publication.issue1pt_PT
degois.publication.titleArthritis Research & Therapypt_PT
dc.relation.publisherversionhttps://arthritis-research.biomedcentral.compt_PT
dc.contributor.authorManica, Santiago Rodrigues-
dc.contributor.authorSepriano, Alexandre-
dc.contributor.authorPimentel-Santos, Fernando-
dc.contributor.authorGouveia, Nélia-
dc.contributor.authorBarcelos, Anabela-
dc.contributor.authorBranco, Jaime C.-
dc.contributor.authorBernardes, Miguel-
dc.contributor.authorFerreira, Raquel Miriam-
dc.contributor.authorVieira de Sousa, Elsa Cristina-
dc.contributor.authorBarreira, Sofia-
dc.contributor.authorVinagre, Filipe-
dc.contributor.authorRoque, Raquel-
dc.contributor.authorSantos, Helena-
dc.contributor.authorMadeira, Nathalie-
dc.contributor.authorRovisco, João-
dc.contributor.authorDaniel, Alexandra-
dc.contributor.authorRamiro, Sofia-
dc.date.accessioned2021-03-01T17:38:10Z-
dc.date.available2021-03-01T17:38:10Z-
dc.date.issued2020-
dc.identifier.citationArthritis Res Ther. 2020 Aug 21;22(1):195pt_PT
dc.identifier.issn1478-6354-
dc.identifier.urihttp://hdl.handle.net/10451/46594-
dc.description© The Author(s). 2020 Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License,which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you giveappropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate ifchanges were made. The images or other third party material in this article are included in the article's Creative Commonslicence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commonslicence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtainpermission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/.The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to thedata made available in this article, unless otherwise stated in a credit line to the data.pt_PT
dc.description.abstractBackground: To investigate whether the reason to discontinue the first TNF inhibitor (TNFi) affects the response to the second TNFi in axial spondyloarthritis (axSpA). Methods: Patients with axSpA from the Rheumatic Diseases Portuguese Register (ReumaPt), who discontinued their first TNFi and started the second TNFi between June 2008 and May 2018, were included. Response was assessed by the Ankylosing Spondylitis Disease Activity Score (ASDAS) clinically important improvement (ASDAS-CII), major important improvement (ASDAS-MI), low disease activity (ASDAS-LDA), and inactive disease (ASDAS-ID). The reason for discontinuation of the first TNFi was defined, according to ASDAS-CII as primary failure (no response ≤ 6 months), secondary failure (response ≤ 6 months but lost thereafter), adverse events, and others. The association between the reason for discontinuation of the first TNFi and response to the second TNFi over time was assessed in multivariable generalized equation (GEE) models. Results: In total, 193 patients were included. The reason for discontinuation of the first TNFi did not influence the response to the second TNFi, according to the ASDAS-CII. However, a difference was found with more stringent outcomes, e.g., there was a higher likelihood to achieve ASDAS-ID with the second TNFi for patients discontinuing the first TNFi due to secondary failure (OR 7.3 [95%CI 1.9; 27.7]), adverse events (OR 9.1 [2.5; 33.3]), or other reasons (OR 7.7 [1.6; 37.9]) compared to primary failure. Conclusion: Patients with axSpA with secondary failure to their first TNFi, compared to those with primary failure, have a better response to the second TNFi according to stringent outcomes.pt_PT
dc.description.sponsorshipThis work was supported by a research grant from Merck Sharp & Dohme Corp., a division of Merck & Co., Inc., Kenilworth, NJ, USA [IIS# 57763]. AS is supported by a doctoral grant from “Fundação para a Ciência e Tecnologia”(SFRH/BD/108246/2015)pt_PT
dc.language.isoengpt_PT
dc.publisherSpringer Naturept_PT
dc.relationinfo:eu-repo/grantAgreement/FCT//SFRH%2FBD%2F108246%2F2015/PTpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectASpt_PT
dc.subjectAnkylosing spondylitispt_PT
dc.subjectSpondyloarthritispt_PT
dc.subjectSwitchpt_PT
dc.subjectTNFipt_PT
dc.subjectTreatmentpt_PT
dc.subjectaxSpApt_PT
dc.subjectbDMARDpt_PT
dc.subjectnr-axSpApt_PT
dc.subjectr-axSpApt_PT
dc.titleEffectiveness of switching between TNF inhibitors in patients with axial spondyloarthritis : is the reason to switch relevant?pt_PT
dc.typearticlept_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.peerreviewedyespt_PT
degois.publication.volume22pt_PT
dc.identifier.doi10.1186/s13075-020-02288-8pt_PT
dc.identifier.eissn1478-6362-
Aparece nas colecções:FM-CUR-Artigos em Revistas Internacionais
IMM - Artigos em Revistas Internacionais

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