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The occurrence of multiple treatment switches in axial spondyloarthritis. Results from five Nordic rheumatology registries.
Di Giuseppe, Daniela; Lindström, Ulf; Aaltonen, Kalle; Relas, Heikki; Provan, Sella; Gudbjornsson, Bjorn; Hetland, Merete Lund; Askling, Johan; Kauppi, Markku; Geirsson, Arni Jon; Chatzidionysiou, Katerina; Jørgensen, Tanja Schjødt; Dreyer, Lene; Michelsen, Brigitte; Jacobsson, Lennart; Glintborg, Bente.
Afiliación
  • Di Giuseppe D; Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm.
  • Lindström U; Department of Rheumatology and Inflammation Research, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
  • Aaltonen K; Ministry of Social Affairs and Health, Pharmaceuticals Pricing Board.
  • Relas H; Departments of Medicine and Rheumatology, Helsinki University Hospital (ROB-FIN), Helsinki, Finland.
  • Provan S; Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.
  • Gudbjornsson B; Faculty of Medicine, Centre for Rheumatology Research (ICEBIO), Landspitali University Hospital, University of Iceland, Reykjavik, Iceland.
  • Hetland ML; DANBIO and Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre of Head and Orthopedics, Copenhagen University Hospital.
  • Askling J; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Kauppi M; Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
  • Geirsson AJ; Department of Rheumatology, Päijät-Häme Central Hospital, Lahti, Finland.
  • Chatzidionysiou K; Department of Rheumatology, University Hospital, Reykjavik, Iceland.
  • Jørgensen TS; Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
  • Dreyer L; The Parker Institute, Copenhagen University Hospital, Copenhagen.
  • Michelsen B; Department of Rheumatology, Aalborg University Hospital, Denmark.
  • Jacobsson L; Department of Rheumatology and Research, Diakonhjemmet Hospital, Oslo.
  • Glintborg B; Division of Rheumatology, Department of Medicine, Sørlandet Sykehus, Kristiansand, Norway.
Rheumatology (Oxford) ; 61(9): 3647-3656, 2022 08 30.
Article en En | MEDLINE | ID: mdl-34940795
OBJECTIVES: In axial spondyloarthritis (axSpA), switching between multiple biologic or targeted synthetic (b/ts-) DMARDs might indicate difficult-to-treat disease. We aimed to explore the occurrence of multiple switching in routine care axSpA patients using various definitions, and to identify associated clinical characteristics upon start of first b/tsDMARD (baseline). METHODS: Observational cohort study including patients with axSpA starting a first-ever b/tsDMARD 2009-2018 based on data from five biologic registries (Denmark/Sweden/Finland/Norway/Iceland). Comorbidities and extra-articular manifestations were identified through linkage to national registries. Multi-switching was defined in overlapping categories according to b/tsDMARD treatment history: treatment with ≥3, ≥4 or ≥5 b/tsDMARDs during follow-up. We explored the cumulative incidence of patients becoming multi-switchers with ≥3 b/tsDMARDs stratified by calendar-period (2009-2011, 2012-2013, 2014-2015, 2016-2018). In the subgroup of patients starting a first b/tsDMARD 2009-2015, baseline characteristics associated with multi-switching (within 3 years' follow-up) were explored using multiple logistic regression analyses. RESULTS: Among 8398 patients included, 6056 patients (63% male, median age 42 years) started a first b/tsDMARD in 2009-2015, whereof proportions treated with ≥3, ≥4 or ≥5 b/tsDMARDs within 3 years' follow-up were 8%, 3% and 1%, respectively. Calendar-period did not affect the cumulative incidence of multi-switching. Baseline characteristics associated with multi-switching (≥3 b/tsDMARDs) were female gender, shorter disease duration, higher patient global score, comorbidities and having psoriasis but not uveitis. CONCLUSION: In this large Nordic observational cohort of axSpA patients, multiple switching was frequent with no apparent time-trend. Clinical associated factors included gender, but also previous comorbidities and extra-articular manifestations illustrating the ongoing challenge of treating this patient group.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Reumatología / Productos Biológicos / Espondiloartritis / Espondiloartritis Axial Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Reumatología / Productos Biológicos / Espondiloartritis / Espondiloartritis Axial Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2022 Tipo del documento: Article