Abstract Introduction Connective Tissue Diseases (CTDs) are systemic autoimmune
conditions characterized by frequent lung involvement. This usually takes the form of …

The diagnostic assessment of patients with Interstitial Lung Disease (ILD) can be
challenging due to the large number of possible causes. Moreover, the diagnostic approach …

Background The gender–age–physiology (GAP) model was developed to predict the risk of
death. Comorbidities are common in idiopathic pulmonary fibrosis (IPF) and may impact on …

Background Patients with idiopathic pulmonary fibrosis (IPF) frequently have multiple
comorbidities, which may influence survival but go under-recognised in clinical practice. We …

Guidelines of the Polish Respiratory Society for diagnosis and treatment of idiopathic pulmonary
fibrosis Page 1 PRACA ORYGINALNA 42 GUIDELINES AND RECOMMENDATIONS …

Idiopathic pulmonary fibrosis (IPF) is a chronic and devastating disease of unknown
etiology, characterized by irreversible morphological changes, ultimately leading to lung …

Idiopathic pulmonary fibrosis (IPF) is characterized by progressive parenchymal scarring,
leading to dyspnoea, respiratory failure and premature death. Although IPF is confined to the …

Background Our study examined whether prevalent and incident comorbidities are
increased in idiopathic pulmonary fibrosis (IPF) patients when compared to matched chronic …

Background Pulmonary hypertension (PH) is a known co-morbidity in West Highland white
terriers (WHWTs) affected with canine idiopathic pulmonary fibrosis (CIPF). The pulmonary …

Idiopathic pulmonary fibrosis (IPF) represents a fibrotic interstitial lung disease characterized
by uncertain etiology and poor prognosis. Over the years, the path to effective treatments …