Abstract

Introduction/objectivesThe objective of this study is to describe the treatment patterns and use of healthcare resources in a cohort of Colombian patients with rheumatoid arthritis (RA) treated with biological disease-modifying antirheumatic drugs (bDMARDs) or tofacitinib.MethodThis is a descriptive study from a retrospective cohort of patients diagnosed with RA who were treated with bDMARDs or tofacitinib after failure of conventional DMARDs (cDMARDs) or first bDMARD. Patients who were receiving pharmacological treatment between 01 January 2014 and 30 June 2018 were included. The analysis is through the revision of claim database and electronical medical records. Demographic and clinical data were collected. The costs of healthcare resources were estimated from the billing expense of healthcare service provider.ResultsWe evaluated 588 RA patients on treatment with bDMARDs (n = 505) or tofacitinib (n = 83), most of them were in combination with cDMARDs (85.4%). The 88.1% were females and mean age was 57.3 ± 12.5 years. The median evolution of RA since diagnosis was 9 years (IQR:4–17.2). The mean duration of use during follow-up of the bDMARDs or tofacitinib was similar, with a mean of 9.8 ± 1.9 months. It was identified that 394 (67.0%) discontinued therapy. The average annual direct cost of care per patient was USD 8997 ± 2172, where 97.2% was due to drug costs. The average annual cost of treatment per patient with bDMARDs was USD 8604 and tofacitinib was USD 6377.ConclusionsIn the face of a first failure of cDMARD, bDMARDs are frequently added. A high frequency of patients do not persist treatment during the first year of follow-up. The pharmacological treatment is the most representative cause of healthcare costs.Key Points• Rheumatoid arthritis is a disease with a high burden of comorbidities, complications, and worse health-related quality of life and is associated with elevated healthcare costs.• The biological disease-modifying antirheumatic drugs or tofacitinib medications are indicated for those with significant progression of the disease and when there is a need for alternatives to achieve low levels of activity and remission.• Patients with rheumatoid arthritis treated with biological disease-modifying antirheumatic drugs or tofacitinib represent a significant economic burden to the health system, especially in the costs derived from pharmacological treatment.

Highlights

  • Rheumatoid arthritis (RA) is a chronic, progressive autoimmune disease characterized by persistent synovial and systemic inflammation associated with joint destruction

  • The biological disease-modifying antirheumatic drugs or tofacitinib medications are indicated for those with significant progression of the disease and when there is a need for alternatives to achieve low levels of activity and remission

  • The following inclusion criteria were considered: patients of either sex, older than 18 years, with a diagnosis of RA based on the International Classification of Diseases (ICD-10) codes M06.9, M0.690-M06.99, M05, and M06.0 and their subclassifications, who have not responded to conventional Disease-modifying antirheumatic drugs (DMARDs) (cDMARDs) or who have received only a first biological disease-modifying antirheumatic drugs (bDMARDs), who began treatment with a bDMARD or tofacitinib after 1 January 2014, and who have been on the medication for more than 6 months

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Summary

Introduction

Rheumatoid arthritis (RA) is a chronic, progressive autoimmune disease characterized by persistent synovial and systemic inflammation associated with joint destruction. It has an estimated prevalence between 0.5% and 1% in the adult population, mainly affecting women and the elderly [1, 2]. Disease-modifying antirheumatic drugs (DMARDs) are available for pharmacological treatment [3,4,5,6] Clin Rheumatol (2021) 40:1273–1281 been classified according to their origin as biological (bDMARD) and conventional (cDMARD). The bDMARDs are used as a second line in patients who have not responded to cDMARDs, but with higher costs and incidence of adverse effects. The objective of the therapy is to control and reduce synovitis and systemic inflammation, prevent joint damage, improve quality of life, and reduce symptoms with improvement in the disability [1, 7]

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