Measuring Different Care Approaches for Rheumatoid Arthritis
Other-Types-of-Arthritis-7.0-1
Scientific Study Title:
Testing of System-Level Performance Measures for Inflammatory Arthritis
Start Date:
End Date:
Research Category
Claire Barber-Website Headshot-400x400
Claire Barber
Research Scientist, Rheumatology, MD, PhD, FRCPC
Diane Lacaille-Website Headshot-400x400
Diane Lacaille
MDCM, MHSc, FRCPC, Scientific Director, Rheumatology
Cheryl Barnabe-Website Headshot-400x400
Cheryl Barnabe
Senior Scientist, Rheumatology, MD, MSc, FRCPC
Glen Hazlewood-Website Headshot-400x400
Glen Hazlewood
Research Scientist, Rheumatology, MD, PhD, FRCPC

Why do this research?

Reason For Research

Over one million Canadians have inflammatory arthritis (IA). There are a few types of IA, but the most common type in adults is rheumatoid arthritis (RA). Early access to the right treatment for patients with RA can improve their outcomes, reducing their symptoms and improving their quality of life. However, in many regions of Canada, it is challenging to provide high-quality care in a timely way because there are too few rheumatologists. In response to this, the Arthritis Alliance of Canada (AAC), an organization of over 36 Canadian arthritis groups, developed ‘Models of Care for Inflammatory Arthritis’. The Models of Care highlight best practices for early diagnosis and treatment using a set of quality measures. We did this research study with the AAC to see how well different healthcare models for patients with RA were doing in meeting four key quality measures.

Methodology

Execution of Research

We evaluated how well RA care is managed across five Canadian clinical sites in Newfoundland, Ontario, and Alberta, including two sites serving Indigenous populations. We looked at four quality measures:
1) how long patients waited to see a rheumatologist,
2) how many patients had yearly follow-up appointments,
3) how many patients were taking medications known to slow down the disease (called disease-modifying antirheumatic drugs or DMARDs), and
4) how quickly patients started on DMARD therapy after being diagnosed.

Findings & Next Steps

We had some challenges in figuring out how well different care models were doing because not all of them kept track of their data in the same way, or for long enough. For example, not all models had complete records about how long patients waited to see a rheumatologist. The waiting time was very different among the sites, from 21 to 75 days. Only two sites could tell us how many of their patients came back for yearly check-ups. Those rates were between 83% and 100%. When it came to patients taking DMARDs and how quickly they started taking them after diagnosis, only three sites provided enough information to evaluate. This data showed 90% to 100% of patients on DMARDs and median time to start these drugs was zero days.

This study consists of 4 sub-projects dedicated to achieving our overall goals. Click below for more information about each sub-project:

Related Publications

  • Barber CEH, Thorne JC, Ahluwalia V, Burt J, Lacaille D, Marshall DA, Hazlewood GS, Mosher D, Denning L, Szamko I, Chin R, Hamilton S, Benseler S, Twilt M, Shiff NJ, Bykerk V, Homik J, Barnabe C. (2018). Feasibility of Measurement and Adherence to System Performance Measures for Rheumatoid Arthritis in 5 Models of Care. The Journal of rheumatology, 45(11), 1501–1508. https://doi.org/10.3899/jrheum.171284

Related Research