Real-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 study.


Journal

Clinical rheumatology
ISSN: 1434-9949
Titre abrégé: Clin Rheumatol
Pays: Germany
ID NLM: 8211469

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 07 05 2021
accepted: 23 08 2021
revised: 29 07 2021
pubmed: 4 9 2021
medline: 6 1 2022
entrez: 3 9 2021
Statut: ppublish

Résumé

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. 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. 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 TNFα 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. The real-world data in PsA patients receiving anti-TNF treatment showed improvement in WPAI, QoL, and disease activity over 9 months of treatment. NCT02028169 Key Points • 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.

Identifiants

pubmed: 34477993
doi: 10.1007/s10067-021-05893-3
pii: 10.1007/s10067-021-05893-3
doi:

Substances chimiques

Antirheumatic Agents 0
Tumor Necrosis Factor Inhibitors 0
Tumor Necrosis Factor-alpha 0
Adalimumab FYS6T7F842
Etanercept OP401G7OJC

Banques de données

ClinicalTrials.gov
['NCT02028169']

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

85-94

Informations de copyright

© 2021. International League of Associations for Rheumatology (ILAR).

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Auteurs

Omer Karadag (O)

School of Medicine, Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Turkey. omerkaradag@ymail.com.

Ediz Dalkilic (E)

School of Medicine, Department of Internal Medicine, Division of Rheumatology, Uludag University, Bursa, Turkey.

Gizem Ayan (G)

School of Medicine, Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Turkey.

Orhan Kucuksahin (O)

Ankara City Hospital - School of Medicine, Department of Internal Medicine, Division of Rheumatology, Ankara Yildirim Beyazit University, Ankara, Turkey.

Timucin Kasifoglu (T)

School of Medicine, Department of Internal Medicine, Division of Rheumatology, Eskisehir Osmangazi University, Eskisehir, Turkey.

Neslihan Yilmaz (N)

Istanbul Florence Nightingale Hospital, Department of Rheumatology, Demiroglu Bilim University, Istanbul, Turkey.

Suleyman Serdar Koca (SS)

School of Medicine, Department of Internal Medicine, Division of Rheumatology, Firat University, Elazig, Turkey.

Veli Yazisiz (V)

School of Medicine, Department of Internal Medicine, Division of Rheumatology, Akdeniz University, Antalya, Turkey.

Pinar Talu Erten (PT)

Medical Park, Department of Internal Medicine, Division of Rheumatology, Izmir Economy University, Izmir, Turkey.

Mehmet Sayarlioglu (M)

Department of Internal Medicine, Division of Rheumatology, Liv Hospital Samsun, Samsun, Turkey.

Mustafa Ender Terzioglu (ME)

School of Medicine, Department of Internal Medicine, Division of Rheumatology, Akdeniz University, Antalya, Turkey.

Sukran Erten (S)

Ankara City Hospital - School of Medicine, Department of Internal Medicine, Division of Rheumatology, Ankara Yildirim Beyazit University, Ankara, Turkey.

Umut Kalyoncu (U)

School of Medicine, Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Turkey.

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