ILD differential diagnosis

interstitial lung disease: A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of pulmonary alveoli that extends to the interstitium and beyond leading to diffuse pulmonary fibrosis. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features.

Summary Statistics

Key figures

All Female Male
Number of individuals 101473 54827 46646
Unadjusted prevalence (%) 39.02 37.31 41.25
Mean age at first event (years) 46.99 44.13 50.36

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 0.05 5.54 [5.16, 5.96] <1e-100 13821
15 years 0.03 7.02 [6.58, 7.48] <1e-100 12504
5 years 0.01 14.51 [13.46, 15.65] <1e-100 7984
1 year 0.01 38.12 [33.07, 43.93] <1e-100 4269

Correlations

Index endpoint: ILD_DIFF_DG – ILD differential diagnosis
GWS hits:

Survival analyses between endpoints

Plot

before ILD differential diagnosis
after ILD differential diagnosis

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after ILD differential diagnosis