Mortality in idiopathic inflammatory myopathy: Results from a Swedish nationwide population-based cohort study
Annals of Rheumatic Diseases Aug 22, 2017
Dobloug GC, et al. – This population–based study highlighted the mortality in patients with idiopathic inflammatory myopathies (IIMs). Collected data represented that mortality was increased in patients with contemporary IIM. Within a year of diagnosis, the increased mortality was reported, which calls for extra vigilance during the first year of IIM diagnosis.
Methods
- With the aid of healthcare registers, patients diagnosed with IIM between 2002 and 2011 and general population comparators were selected.
- For follow–up, they were linked to the cause of death register.
Results
- 224 (31%) of the 716 patients with IIM and 870 (12%) of the 7100 general population died during follow–up.
- This corresponded to a mortality rate of 60/1000 person–years in IIM and 20/1000 person–years in the general population.
- The cumulative mortality at 1 year after diagnosis was 9% in IIM and 1% in the general population, and increased in both IIM and the general population with time.
- The overall hazard ratio (HR) 95%CI of death comparing IIM with the general population was 3.7 (3.2 to 4.4).
- When the authors stratified on time since diagnosis, they reported an increase in mortality already within the first year of diagnosis compared with the general population, HR 9.6 (95% CI 6.9 to 13.5).
- This HR then plateaued around 2 after >10 years with the disease, although the estimates were not statistically significant.
- The common causes of death were malignancies, diseases of the circulatory and respiratory system.
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