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Fig. 3 | Respiratory Research

Fig. 3

From: Estimates of epidemiology, mortality and disease burden associated with progressive fibrosing interstitial lung disease in France (the PROGRESS study)

Fig. 3Fig. 3

Overall survival for PF-ILD. a Overall survival among all patients, and by b sex, c age, and d diagnosis subgroup. Overall survival was defined as the time in years from the date of progression to the date of death due to any cause. Shading indicates 95% Hall–Wellner band. ILD interstitial lung disease, MCTD mixed connective tissue disease, PF-ILD progressive fibrosing interstitial lung disease, RA rheumatoid arthritis, SSc systemic sclerosis

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