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dc.contributor.authorØrnbjerg L.M.
dc.contributor.authorRugbjerg K.
dc.contributor.authorGeorgiadis S.
dc.contributor.authorRasmussen S.H.
dc.contributor.authorLindström U.
dc.contributor.authorPavelka K.
dc.contributor.authorYilmaz N.
dc.date.accessioned2024-02-04T13:30:21Z
dc.date.available2024-02-04T13:30:21Z
dc.date.issued2023
dc.identifier.issn0315162X
dc.identifier.urihttps://doi.org/10.3899/jrheum.220459
dc.identifier.urihttp://hdl.handle.net/11446/4899
dc.description.abstractObjective. To investigate the distribution of patient-reported outcomes (PROs) in patients with axial spondyloarthritis (axSpA) initiating a tumor necrosis factor inhibitor (TNFi), to assess the proportion reaching PRO “remission” across registries and treatment series, and to compare patients registered to fulfill the modified New York (mNY) criteria for ankylosing spondylitis (AS) vs patients with nonradiographic axSpA (nr-axSpA). Methods. Fifteen European registries contributed PRO scores for pain, fatigue, patient global assessment (PtGA), Bath Ankylosing Spondylitis (AS) Disease Activity Index (BASDAI), Bath AS Functional Index (BASFI), and Health Assessment Questionnaire (HAQ) from 19,498 patients with axSpA. Changes in PROs and PRO remission rates (definitions: ? 20 mm for pain, fatigue, PtGA, BASDAI, and BASFI; ? 0.5 for HAQ) were calculated at 6, 12, and 24 months of treatment. Results. Heterogeneity in baseline characteristics and outcomes between registries were observed. In pooled data, 6 months after the start of a first TNFi, pain score was reduced by approximately 60% (median at baseline/6/12/24 months: 65/25/20/20 mm) in patients on treatment. Similar patterns were observed for fatigue (68/32/30/25 mm), PtGA (66/29/21/20 mm), BASDAI (58/26/21/19 mm), BASFI (46/20/16/16 mm), and HAQ (0.8/0.4/0.2/0.2). Patients with AS (n = 3281) had a slightly better response than patients with nr-axSpA (n = 993). The Lund Efficacy Index (LUNDEX)-adjusted remission rates at 6 months for pain/fatigue/PtGA/BASDAI/BASFI/HAQ were 39%/30%/38%/34%/35%/48% for the AS cohort and 30%/21%/26%/24%/33%/47% for the nr-axSpA cohort. Better PRO responses were seen with a first TNFi compared to a second and third TNFi. Conclusion. Patients with axSpA starting a TNFi achieved high PRO remission rates, most pronounced in those fulfilling the mNY criteria and for the first TNFi. © 2023 The Journal of Rheumatology.en_US
dc.description.sponsorshipNovartisen_US
dc.description.sponsorshipOn behalf of the EuroSpA Scientific Committee, the authors acknowledge Novartis Pharma AG and IQVIA for supporting the EuroSpA collaboration.en_US
dc.description.sponsorshipThe European Spondyloarthritis Research Collaboration Network was financially supported by Novartis Pharma AG. Novartis had no influence on the data collection, statistical analyses, manuscript preparation, or decision to submit the manuscript. 1L.M. Ørnbjerg, MD, PhD, K. Rugbjerg, MSc, PhD, S. Georgiadis, PhD, S.H. Rasmussen, PhD, Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; 2U. Lindström, MD, PhD, Department of Rheumatology and Inflammation Research, University of Gothenburg Sahlgrenska Academy, Gothenburg, Sweden; 3K. Pavelka, MD, PhD, Institute of Rheumatology, and Department of Rheumatology, First Faculty of Medicine, Charlesen_US
dc.language.isoengen_US
dc.publisherJournal of Rheumatologyen_US
dc.relation.ispartofJournal of Rheumatologyen_US
dc.identifier.doi10.3899/jrheum.220459
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectaxial spondyloarthritisen_US
dc.subjectpatient-reported outcome measuresen_US
dc.subjecttumor necrosis factor inhibitorsen_US
dc.subjectadalimumaben_US
dc.subjectcertolizumab pegolen_US
dc.subjectetanercepten_US
dc.subjectgolimumaben_US
dc.subjectinfliximaben_US
dc.subjecttumor necrosis factor inhibitoren_US
dc.subjecttumor necrosis factoren_US
dc.subjecttumor necrosis factor inhibitoren_US
dc.subjectadulten_US
dc.subjectArticleen_US
dc.subjectaxial spondyloarthritisen_US
dc.subjectBath ankylosing spondylitis disease activity indexen_US
dc.subjectBath ankylosing spondylitis functional indexen_US
dc.subjectclinical outcomeen_US
dc.subjectEuropeen_US
dc.subjectfatigueen_US
dc.subjectfemaleen_US
dc.subjectHealth Assessment Questionnaireen_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectnon-radiographic axial spondyloarthritisen_US
dc.subjectpainen_US
dc.subjectpain assessmenten_US
dc.subjectpatient-reported outcomeen_US
dc.subjectremissionen_US
dc.subjecttreatment responseen_US
dc.subjectankylosing spondylitisen_US
dc.subjectfatigueen_US
dc.subjectnon-radiographic axial spondyloarthritisen_US
dc.subjectpainen_US
dc.subjectspondylarthritisen_US
dc.subjecttreatment outcomeen_US
dc.subjectFatigueen_US
dc.subjectHumansen_US
dc.subjectNon-Radiographic Axial Spondyloarthritisen_US
dc.subjectPainen_US
dc.subjectSpondylarthritisen_US
dc.subjectSpondylitis, Ankylosingen_US
dc.subjectTreatment Outcomeen_US
dc.subjectTumor Necrosis Factor Inhibitorsen_US
dc.subjectTumor Necrosis Factor-alphaen_US
dc.titleOne-Third of European Patients With Axial Spondyloarthritis Reach Pain Remission With Routine Care Tumor Necrosis Factor Inhibitor Treatmenten_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue8en_US
dc.identifier.volume50en_US
dc.identifier.startpage1009en_US
dc.identifier.endpage1019en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempØrnbjerg, L.M., Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; Rugbjerg, K., Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; Georgiadis, S., Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; Rasmussen, S.H., Copenhagen Center for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre of Head and Orthopaedics, Copenhagen University Hospital, Glostrup, Denmark; Lindström, U., Department of Rheumatology and Inflammation Research, University of Gothenburg Sahlgrenska Academy, Gothenburg, Sweden; Pavelka, K., Institute of Rheumatology, Department of Rheumatology, First Faculty of Medicine, Charles University, Prague, Czech Republic; Yilmaz, N., Department of Rheumatology, Demiroglu Bilim University, Istanbul, Turkey; Favalli, E.G., Division of Clinical Rheumatology, ASST Gaetano Pini-CTO Institute, Milan, Italy; Nissen, M.J., Department of Rheumatology, Geneva University Hospital, Geneva, Switzerland; Michelsen, B.,en_US
dc.identifier.pmid36455943en_US
dc.identifier.scopus2-s2.0-85166052278en_US
dc.authorscopusid24069275900
dc.authorscopusid24475168600
dc.authorscopusid55453151500
dc.authorscopusid57844942500
dc.authorscopusid56624176500
dc.authorscopusid57209490653
dc.authorscopusid35489690300


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