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dc.contributor.authorKaradag O.
dc.contributor.authorDalkilic E.
dc.contributor.authorAyan G.
dc.contributor.authorKucuksahin O.
dc.contributor.authorKasifoglu T.
dc.contributor.authorYilmaz N.
dc.contributor.authorKoca S.S.
dc.date.accessioned2024-02-04T13:30:04Z
dc.date.available2024-02-04T13:30:04Z
dc.date.issued2022
dc.identifier.issn07703198
dc.identifier.urihttps://doi.org/10.1007/s10067-021-05893-3
dc.identifier.urihttp://hdl.handle.net/11446/4834
dc.description.abstractObjectives: To understand change in work productivity, activity impairment, quality of life (QoL), and disease activity in patients with psoriatic arthritis (PsA) receiving anti-tumor necrosis factor (anti-TNF) treatment. Method: One hundred twenty patients with PsA receiving anti-TNF therapy were recruited to this noninterventional, observational study. Work disability was assessed via the Work Productivity and Activity Impairment (WPAI) questionnaire and disease activity was calculated via the 28-joint Disease Activity Score using C-reactive protein (DAS28-CRP) and Disease Activity Index for Psoriatic Arthritis with 28 joints (DAPSA28) score. Patient-reported outcomes (PROs), from visual analog scores and Health Assessment Questionnaire-Disability Index scores, were evaluated to understand the clinical effectiveness at baseline and every 3 months until the month-9 final visit. The American College of Rheumatology (ACR)20/50/70 response criteria were assessed at month 9. Results: A total of 120 patients (females, n = 73) were enrolled in the study. Mean (SD) age and disease duration were 41.6 ± 11.1 years and 6.9 ± 6.5 years, respectively. The most commonly used TNF? inhibitor was adalimumab (42.4%), followed by etanercept (25.8%). All WPAI questionnaire parameters were reduced at the follow-up visits compared with baseline (p < 0.001 for all). PROs and disease activity indicators (DAS28-CRP and DAPSA28) significantly improved during the course of anti-TNF treatments (p < 0.001 for all). Additionally, ACR20/50/70 responses were determined as 86.8%, 63.7%, and 41.8% of patients at the month-9 visit. Conclusions: The real-world data in PsA patients receiving anti-TNF treatment showed improvement in WPAI, QoL, and disease activity over 9 months of treatment. Trial registration: NCT02028169 • Psoriatic arthritis (PsA), with debilitating effects on quality of life, occurs mostly in young adults and has negative impacts on employment status and work productivity.• Early PsA diagnosis and treat-to-target treatment strategies aim to reduce pain and joint damage, as well as improve work productivity.• Real-world data on the impact of treatment with anti-tumor necrosis factor (anti-TNF) agents on work productivity in PsA in the literature is scarce.• Our study of real-world data in patients with PsA receiving anti-TNF treatment showed improvement in work productivity, as well as in clinical and patient-reported outcomes. © 2021, International League of Associations for Rheumatology (ILAR).en_US
dc.description.sponsorshipRoche; AbbVie; UCBen_US
dc.description.sponsorshipOmer Karadag: AbbVie (research grant, consulting fee), Pfizer (research grant, consulting fee), Roche (research grant, consulting fee), Novartis (research grant), Abdi İbrahim (consulting fee), Amgen (consulting fee), Farmanova (consulting fee), Janssen (consulting fee), Lilly (consulting fee), UCB (consulting fee). Ediz Dalkilic: AbbVie (speaker fee), MSD (speaker fee), Roche (speaker fee), Pfizer (speaker fee), UCB (speaker fee), Novartis (speaker fee). Gizem Ayan: None. Orhan Kucuksahin: None. Timucin Kasifoglu: AbbVie, Amgen, Roche, MSD, Novartis, Pfizer, and UCB (speaker and consulting fees). Neslihan Yilmaz: AbbVie (speaker fee), Pfizer (speaker fee), UCB (speaker fee), Roche (speaker fee), Janssen (speaker fee). Suleyman Serdar Koca: AbbVie (speaker fee), Pfizer (speaker fee), Roche (speaker fee), UCB (speaker fee), Novartis (speaker fee), Amgen (speaker fee), Pharmactive (speaker fee), MSD (speaker fee). Veli Yazisiz: AbbVie (consulting fee), Pfizer (consulting fee), UCB (consulting fee). Pinar Talu Erten: None. Mehmet Sayarlioglu: Genzyme (speaker fee), MSD (consulting fee), Novartis (research grant). Mehmet Ender Terzioglu: AbbVie, Pfizer, Novartis, Boehringer Ingelheim, Pharmactive, and UCB (speaker/consulting fee and/or research grant). Sukran Erten: Janssen (speaker fee), Roche (speaker fee), Novartis (speaker fee). Umut Kalyoncu: AbbVie, Pfizer (research grant, speaker, and consulting fee), Janssen (research grant, speaker fee), UCB, Novartis (speaker and consulting fee), Lilly (consulting fee).en_US
dc.language.isoengen_US
dc.publisherSpringer Science and Business Media Deutschland GmbHen_US
dc.relation.ispartofClinical Rheumatologyen_US
dc.identifier.doi10.1007/s10067-021-05893-3
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectACR20/50/70en_US
dc.subjectAnti-TNFen_US
dc.subjectDAPSA28en_US
dc.subjectDAS28en_US
dc.subjectPsoriatic arthritisen_US
dc.subjectWork disabilityen_US
dc.subjectadalimumaben_US
dc.subjectC reactive proteinen_US
dc.subjectcertolizumab pegolen_US
dc.subjectcyclosporineen_US
dc.subjectdeflazacorten_US
dc.subjectdiclofenacen_US
dc.subjectetanercepten_US
dc.subjectetodolacen_US
dc.subjectgolimumaben_US
dc.subjecthydroxychloroquineen_US
dc.subjectinfliximaben_US
dc.subjectleflunomideen_US
dc.subjectmeloxicamen_US
dc.subjectmethotrexateen_US
dc.subjectmethylprednisoloneen_US
dc.subjectnaproxenen_US
dc.subjectprednisoloneen_US
dc.subjectsalazosulfapyridineen_US
dc.subjecttumor necrosis factor inhibitoren_US
dc.subjectadalimumaben_US
dc.subjectantirheumatic agenten_US
dc.subjectetanercepten_US
dc.subjecttumor necrosis factoren_US
dc.subjecttumor necrosis factor inhibitoren_US
dc.subjectachilles tendonen_US
dc.subjectadulten_US
dc.subjectageen_US
dc.subjectArticleen_US
dc.subjectclinical effectivenessen_US
dc.subjectclinical outcomeen_US
dc.subjectcomparative studyen_US
dc.subjectcontrolled clinical trialen_US
dc.subjectcontrolled studyen_US
dc.subjectdaily life activityen_US
dc.subjectDAS28en_US
dc.subjectdisease activityen_US
dc.subjectDisease Activity Index for Psoriatic Arthritis with 28 jointsen_US
dc.subjectdisease activity scoreen_US
dc.subjectdisease durationen_US
dc.subjecterythrocyte sedimentation rateen_US
dc.subjectfemaleen_US
dc.subjectfollow upen_US
dc.subjectHealth Assessment Questionnaireen_US
dc.subjectHealth Assessment Questionnaire Disability Indexen_US
dc.subjecthouseholden_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectmulticenter studyen_US
dc.subjectobservational studyen_US
dc.subjectopen studyen_US
dc.subjectpain assessmenten_US
dc.subjectpatient-reported outcomeen_US
dc.subjectphysical activityen_US
dc.subjectpostmarketing surveillanceen_US
dc.subjectproductivityen_US
dc.subjectprospective studyen_US
dc.subjectpsoriatic arthritisen_US
dc.subjectquality of lifeen_US
dc.subjectspinous processen_US
dc.subjectswollen joint counten_US
dc.subjectvisual analog scaleen_US
dc.subjectwork disabilityen_US
dc.subjectpsoriatic arthritisen_US
dc.subjectquality of lifeen_US
dc.subjecttreatment outcomeen_US
dc.subjectyoung adulten_US
dc.subjectAdalimumaben_US
dc.subjectAntirheumatic Agentsen_US
dc.subjectArthritis, Psoriaticen_US
dc.subjectEtanercepten_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectQuality of Lifeen_US
dc.subjectTreatment Outcomeen_US
dc.subjectTumor Necrosis Factor Inhibitorsen_US
dc.subjectTumor Necrosis Factor-alphaen_US
dc.subjectYoung Adulten_US
dc.titleReal-world data on change in work productivity, activity impairment, and quality of life in patients with psoriatic arthritis under anti-TNF therapy: a postmarketing, noninterventional, observational studyen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue1en_US
dc.identifier.volume41en_US
dc.identifier.startpage85en_US
dc.identifier.endpage94en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempKaradag, O., School of Medicine, Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Turkey; Dalkilic, E., School of Medicine, Department of Internal Medicine, Division of Rheumatology, Uludag University, Bursa, Turkey; Ayan, G., School of Medicine, Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Turkey; Kucuksahin, O., Ankara City Hospital – School of Medicine, Department of Internal Medicine, Division of Rheumatology, Ankara Yildirim Beyazit University, Ankara, Turkey; Kasifoglu, T., School of Medicine, Department of Internal Medicine, Division of Rheumatology, Eskisehir Osmangazi University, Eskisehir, Turkey; Yilmaz, N., Istanbul Florence Nightingale Hospital, Department of Rheumatology, Demiroglu Bilim University, Istanbul, Turkey; Koca, S.S., School of Medicine, Department of Internal Medicine, Division of Rheumatology, Firat University, Elazig, Turkey; Yazisiz, V., School of Medicine, Department of Internal Medicine, Division of Rheumatology, Akdeniz University, Antalya, Turkey; Erten, P.T., Medical Park, Department of Internal Medicine, Division of Rheumatology, Izmir Economy University, Izmir, Turkey; Sayarlioglu, M., Department of Internal Medicine, Division of Rheumatology, Liv Hospital Samsun, Samsun, Turkey; Terzioglu, M.E., School of Medien_US
dc.identifier.pmid34477993en_US
dc.identifier.scopus2-s2.0-85114190305en_US
dc.authorscopusid14630767100
dc.authorscopusid6506739457
dc.authorscopusid57192237533
dc.authorscopusid14422446100
dc.authorscopusid8392501600
dc.authorscopusid35489690300
dc.authorscopusid55667445900


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