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Clinical behaviour of patients exposed to organic dust and diagnosed with idiopathic pulmonary fibrosis.

De Sadeleer LaurensStijn E VerledenEls De DyckerJonas YserbytJohny A VerschakelenEric K VerbekenBenoit NemeryGeert M VerledenFrederik HermansBart M VanaudenaerdeWim A Wuyts
Published in: Respirology (Carlton, Vic.) (2018)
Group B patients experienced a better outcome compared with (non-exposed) IPF patients, although worse compared with CHP patients. Antifibrotic treatment in group B resulted in a similar beneficial effect compared with group A. Further research is needed to ascertain the diagnostic designation in this exposed usual interstitial pneumonia (UIP) patient group without other CHP features.
Keyphrases
  • end stage renal disease
  • idiopathic pulmonary fibrosis
  • chronic kidney disease
  • ejection fraction
  • newly diagnosed
  • prognostic factors
  • peritoneal dialysis
  • intensive care unit
  • patient reported
  • drinking water