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Prevalence and prognosis of chronic fibrosing interstitial lung diseases with a progressive phenotype.

Reoto TakeiKevin K BrownYasuhiko YamanoKensuke KataokaToshiki YokoyamaToshiaki MatsudaTomoki KimuraAtsushi SuzukiTaiki FurukawaJunya FukuokaTakeshi JohkohYoshihito GotoYasuhiro Kondoh
Published in: Respirology (Carlton, Vic.) (2022)
Over one-fourth of non-IPF FILD patients develop a progressive phenotype compared to approximately 60% of IPF patients. The survival of non-IPF FILD patients with a progressive phenotype is similar to IPF.
Keyphrases
  • idiopathic pulmonary fibrosis
  • end stage renal disease
  • multiple sclerosis
  • ejection fraction
  • newly diagnosed
  • peritoneal dialysis
  • prognostic factors
  • patient reported outcomes
  • risk factors
  • patient reported