Time to remission in swollen joints is far faster than patient reported outcomes in rheumatoid arthritis: results from the Ontario Best Practices Research Initiative (OBRI)

Publication type
Journal article
Authors
Pope JE, Rampakakis E, Movahedi M, Cesta A, Sampalis JS, Bombardier C
Date published
2021 Feb 01
Journal
Rheumatology
Volume
60
Issue
2
Pages
717-727
Open Access?
No
Abstract

Objectives: RA patients are often not in remission due to patient global assessment of disease activity (PtGA) included in disease activity indices. The aim was to assess the lag of patient-reported outcomes (PROs) after remission measured by clinical disease activity index (CDAI) or swollen joint count (SJC28). Methods: RA patients enrolled in the Ontario Best Practices Research Initiative registry not in low disease state at baseline with at =6 months of follow-up, were included. Low disease state was defined as CDAI = 10, SJC28 = 2, PtGA = 2cm, pain score = 2cm, or fatigue = 2cm. Remission included CDAI = 2.8, SJC28 = 1, PtGA = 1cm, pain score = 1cm, or fatigue = 1cm. Time to first low disease state/remission based on each definition was calculated overall and stratified by early vs established RA. Results: A total of 986 patients were included (age 57.4 (12.9), disease duration 8.3 (9.9) years, 80% women). The median (95% CI) time in months to CDAI = 10 was 12.4 (11.4, 13.6), SJC28 = 2 was 9 (8.2, 10), PtGA = 2cm was 18.9 (16.1, 22), pain = 2cm was 24.5 (19.4, 30.5), and fatigue = 2cm was 30.4 (24.8, 31.7). For remission, the median (95% CI) time in months to CDAI = 2.8 was 46.5 (42, 54.1), SJC28 = 1 was 12.5 (11.4, 13.4), PtGA = 1cm was 39.6 (34.6, 44.8), pain = 1cm was 54.7 (43.6, 57.5) and fatigue = 1cm was 42.6 (36.8, 48). Time to achieving low disease state and remission was generally significantly shorter in early RA compared with established RA with the exception of fatigue. Conclusion: Time to achieving low disease state or remission based on PROs was considerably longer compared with swollen joint count. Treating to a composite target in RA could lead to inappropriate changes in DMARDs.