Login / Signup

Baseline characteristics and comorbidities in the CAnadian REgistry for Pulmonary Fibrosis.

Jolene H FisherM KolbM AlgamdiJ MorissetK A JohannsonS ShaperaP WilcoxT ToM SadatsafaviH ManganasN KhalilN HamblyA J HalaykoA S GershonC D FellG CoxC J Ryerson
Published in: BMC pulmonary medicine (2019)
CTD-ILD, IPF, and unclassifiable ILD made up 80% of ILD diagnoses at ILD referral centers in Canada, while idiopathic NSIP was rare when adhering to recommended diagnostic criteria. CCI had a very narrow distribution across our cohort suggesting it may be a poor discriminator in assessing the impact of comorbidities on patients with ILD.
Keyphrases
  • interstitial lung disease
  • systemic sclerosis
  • idiopathic pulmonary fibrosis
  • rheumatoid arthritis
  • pulmonary fibrosis
  • primary care
  • neuropathic pain