Rheumatic disease in Canada’s Northwest Territories: baseline review and comparative insights
摘要
This study captures baseline demographic and rheumatologic history of patients from Canada’s Northwest Territories (NWT) to improve disease burden understanding, identify potential at-risk populations, and highlight care gaps in a unique and underserved population.
MethodsIn this descriptive study, we collected retrospective data on patients referred from the NWT to Edmonton, Alberta, in 2022–2023, when all established and newly referred rheumatology patients from this region were redirected to receive care in Edmonton. Diagnoses were compared to a 2022–2023 Edmonton rheumatology new-patient cohort.
ResultsThere were 425 patients (70% female) representing 30 communities. Of the 250 patients with documented ethnicity, 69.6%, 25.6%, and 4.8% were of Indigenous, White, and Other descent (including people of Asian and African descent), respectively. The most frequent inflammatory rheumatologic diagnoses among new referrals were rheumatoid arthritis (27.8%), gout (13.9%), and psoriatic arthritis and ankylosing spondylitis (11.1% each, vs. ~ 7% each in the Edmonton-based cohort). There were no new vasculitis cases in the NWT cohort compared to 9.2% of new diagnoses in the Edmonton cohort. Twenty-one percent of patients missed their appointments, and 43% of previously established patients had active disease.
ConclusionThis represents the broadest epidemiologic dataset for NWT patients with rheumatologic diseases, with higher observed proportion of ankylosing spondylitis and psoriatic arthritis and lower observed proportion of vasculitis, compared to the Edmonton cohort. NWT patients face unique barriers around geographic location, transportation, and care delays, compounded by active disease that may disproportionately affect female and Indigenous patients.