Has the incidence of total joint arthroplasty in rheumatoid arthritis decreased in the era of biologics use? A population-based cohort study

Author:

Zhou Vivienne Y12ORCID,Lacaille Diane13,Lu Na1,Kopec Jacek A14,Garbuz Donald S15,Qian Yi6,Aviña-Zubieta J Antonio13,Esdaile John M13,Xie Hui12

Affiliation:

1. Arthritis Research Canada, Vancouver, British Columbia, Canada

2. Faculty of Health Sciences, Simon Fraser University, Vancouver, Canada

3. Division of Rheumatology, Department of Medicine, University of British Columbia, Vancouver, Canada

4. Division of Epidemiology, Biostatistics and Public Health Practice, Department of Medicine, University of British Columbia, Vancouver, Canada

5. Department of Orthopaedics, University of British Columbia, Vancouver, Canada

6. Sauder School of Business, University of British Columbia, Vancouver, Canada

Abstract

Abstract Objectives To determine whether the introduction of biological DMARDs (bDMARDs) was associated with reduced incidences of total hip and knee arthroplasty (THA/TKA) among patients with RA compared with OA. Methods Using a population-based cohort in British Columbia, Canada, RA and OA patients diagnosed between 1995 and 2007 were divided into semi-annual cohorts according to diagnosis date. For each cohort, we calculated 8-year incidence rates of THA and TKA. We compared levels and trends of THA/TKA incidence in RA/OA patients diagnosed during pre-bDMARDs (1995–2001) and post-bDMARDs (2003–2007) periods using interrupted time-series analysis, adjusting for baseline characteristics. Adjusted 8-year total joint arthroplasty incidence estimated for RA/OA cohorts diagnosed five years after bDMARDs introduction were compared with expected rates assuming no bDMARDs introduction, based on extrapolation of pre-bDMARDs trends. Results We identified 60 227 RA and 288 260 OA incident cases. For cohorts diagnosed pre-bDMARDs, 8-year THA/TKA incidence rates increased over time in both RA and OA. For cohorts diagnosed post-bDMARDs, these rates decreased over time in RA but continued to increase for OA. For RA, differences between the post- and pre-bDMARDs secular trends in incidence rates were −0.49 (P = 0.002) for THA and −0.36 (P = 0.003) for TKA, compared with +0.40 (P = 0.006) and +0.54 (P < 0.001), respectively, for OA. For RA cohorts diagnosed five years after bDMARDs introduction, 8-year incidences were 26.9% and 12.6% lower for THA and TKA, respectively, than expected rates. In contrast, corresponding rates in OA were higher by 11.7% and 16.6%, respectively. Conclusion Arthritis onset after bDMARDs introduction is associated with a significant reduction in THA/TKA incidence in RA, but not in OA. The reduction reflects a significant improvement in RA treatment during the biological era.

Funder

Canadian Institute of Health Research

Natural Sciences and Engineering Research Council

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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