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. 2018 Jun 1;4(1):103–114. doi: 10.1007/s41030-018-0056-8

Table 1.

Respondent characteristics

Characteristic All respondents (N = 169)
Classification, n (%)
 ILD expert 69 (40.8)
 Community pulmonologist 100 (59.2)
Years practicing pulmonary medicine, n (%)
 1–5 22 (13.0)
 6–10 35 (20.7)
 11–20 60 (35.5)
 21–30 47 (27.8)
 31–40 5 (3.0)
Professional time spent in direct patient care, n (%)
 21–40% 3 (1.8)
 41–60% 14 (8.3)
 61–80% 36 (21.3)
 81–100% 116 (68.6)
Primary practice setting, n (%)
 Academic 97 (57.4)
 Private practice 41 (24.3)
 Community 30 (17.8)
 Other 1 (0.6)
Patients with IPF in the practice, mean (SD), n 66 (109)
Patients treated with an approved antifibrotic, mean (SD), % 55.2 (28.8)

ILD interstitial lung disease, IPF idiopathic pulmonary fibrosis, SD standard deviation