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Disease progression in idiopathic pulmonary fibrosis with mild physiological impairment: analysis from the Australian IPF registry.

Helen E JoIan GlaspoleYuben MoodleySally ChapmanSamantha EllisNicole GohPeter HopkinsGreg KeirAnnabelle MaharWendy CooperPaul ReynoldsE Haydn WaltersChristopher ZappalaChristopher GraingeHeather AllanSacha MacanshTamera J Corte
Published in: BMC pulmonary medicine (2018)
IPF patients with mild physiological impairment have better survival than patients with moderate-severe disease. Their overall rate of disease progression however, is comparable, suggesting that they are simply at different points in the natural history of IPF disease.
Keyphrases
  • idiopathic pulmonary fibrosis
  • interstitial lung disease
  • early onset
  • rheumatoid arthritis
  • systemic sclerosis
  • free survival