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Table 1 Characteristics of patients at enrolment into the IPF-PRO Registry (n = 662)

From: Predictors of death or lung transplant after a diagnosis of idiopathic pulmonary fibrosis: insights from the IPF-PRO Registry

Age, years

70 (65, 75)

Male

496 (74.9)

White

623 (94.1)

Body mass index, kg/m2

29.0 (26.0, 32.4)

Private insurance

420 (66.4)

Current or former smoker

446 (68.4)

Oxygen use with activity

217 (34.1)

Oxygen use at rest

125 (19.6)

Serologic testing reported at enrolment

 At least one abnormal serologic test reported

184 (27.8)

161

Receiving immunosuppressive or cytotoxic medications

5 (0.8)

Receiving nintedanib or pirfenidone

352 (54.0)

Surgical lung biopsy performed prior to enrolment

176 (30)

Bronchoscopy performed within 12 months of enrolment

60 (10.3)

Prior diagnosis of IPF (confirmed at the enrolling centre)

301 (45)

Diagnostic criteriaa

 Definite IPF

437 (68.8)

 Probable IPF

141 (22.2)

 Possible IPF

57 (9.0)

History of coronary artery disease or congestive heart failure

203 (31.2)

History of pulmonary hypertension

51 (7.9)

Emphysemab

71 (11.2)

Prior hospitalisation (any)

171 (29.3)

 Respiratory related

106 (18.2)

 Non-respiratory related

86 (14.8)

Symptom onset to confirmed diagnosis of IPF at enrolling center, months

14 (7, 29)

Distance to enrolling centre, miles

40 (16, 109)

FVC, % predicted

69.6 (60.1, 79.9)

DLco, % predicted

41.7 (32.2, 50.1)

Prior respiratory hospitalisation

106 (18.2)

 1

84 (12.7)

 2

18 (2.7)

 3

3 (0.5)

 4

1 (0.2)

Composite physiologic index

53.2 (45.7, 60.0)

GAP stage

 I

146 (26.4)

 II

306 (55.2)

 III

102 (18.4)

  1. Data are median (25th, 75th percentile) or n (%). Not all patients provided data on all variables. aAccording to 2011 ATS/ERS/JRS/ALAT diagnostic guidelines [1]. bClinically significant emphysema on HRCT scan (based on the opinion of the investigator)