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Smoldering Rheumatoid Arthritis: Is the Canadian Healthcare System Neglecting a Significant Disease Population?
STEVEN EDWORTHY, MICHEL ZUMMER, STEPHANIE GARNER, GILLES BOIRE, SHARON LeCLERCQ, VIVIAN BYKERK, GUNNER KRAAG, JANET MARKLAND, DIANE THOMAS, JOHN THOMSON, and JAMIE HENDERSON
ABSTRACT. Methods. Rheumatologists were invited to participate by the Canadian Rheumatology Association in an audit entitled the Assessment in Rheumatology (AIR) program. From across Canada, 65 rheumatologists participated. One thousand five hundred ninety-six consecutive patients with RA seen in regular clinics were classified according to 4 states of disease activity: remission, controlled adequately, smoldering, and uncontrolled. Demographics (age, sex, geographic region), therapy (nonsteroidal antiinflammatory drugs, disease modifying antirheumatic drugs, biologicals, steroids), joint counts (tender/swollen), comorbidity, and treatment decisions at the time of the visit were recorded. Data were collected at the time of the visit with personal digital assistants (PDA) and aggregated, without personal identifiers, for analysis in SPSS. Results. The majority of patients had "smoldering" (29%) or "uncontrolled" disease (23%), with the remainder in "remission" (15%) or "controlled adequately" (33%) at the time of their visit. Following the appointment, the uncontrolled group had a 100% increase (from 10.4% to 23.4%) in the addition of biological agents; however, there was no significant increase in the rates for those with smoldering disease (19.4% to 20.5%). Conclusion. Despite Canada's universal healthcare system, current treatment regimens may not be optimized on the basis of disease activity. A large proportion of patients with RA (29%) seen in Canadian rheumatology practices may be experiencing unnecessary disease for a variety of reasons. (First Release June 15 2008; J Rheumatol 2008;35:1506–12) Key Indexing Terms:
RHEUMATOID ARTHRITIS
From the University of Calgary, Calgary, Alberta; Université de Montréal, Montreal; Université de Sherbrooke, Sherbrooke, Quebec; University of Toronto, Toronto; University of Ottawa, Ottawa, Ontario; University of Saskatchewan, Saskatoon, Saskatchewan; and the University of New Brunswick, Fredericton, New Brunswick, Canada. Sponsored by the Canadian Rheumatology Association (CRA) through an unrestricted educational grant from Amgen-Wyeth. S. Edworthy, MD; S. Garner, BSc; S. LeClercq, MD; D. Thomas, MD, University of Calgary; M. Zummer, MD, Université de Montréal; G. Boire, MD, Université de Sherbrooke; V. Bykerk, MD, University of Toronto; G. Kraag, MD; J. Thomson, MD, University of Ottawa; J. Markland, University of Saskatchewan; J. Henderson, MD, University of New Brunswick. Address reprint requests to Dr. S. Edworthy, University of Calgary, 3330 Hospital Dr. NW, Calgary, Alberta T2N 4N1, Canada. E-mail: sedworth@ucalgary.ca Accepted for publication March 12, 2008. |