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. 2018 Dec;10(12):6660–6669. doi: 10.21037/jtd.2018.11.16

Table 2. Baseline characteristics and clinical course of 23 newly diagnosed IPF patients.

Patients, number Gender Age (years) Diagnosis Stage of fibrosis (GAP score) Type to the outcome Outcome itself
1 F 65 IPF I Slow progression Died
2 F 76 IPF II Slow progression Died, CVI
3 M 69 IPF III Slow progression Died, CVI
4 M 50 IPF I Slow progression Alive, dementia
5 F 68 IPF II Slow progression Died
6 M 87 IPF II Fast progression Died
7 F 66 IPF I Slow progression Alive, stable disease
8 M 73 IPF/Ca II Slow progression Died, Ac. exacerbation
9 F 68 IPF II Slow progression Alive
10 M 63 IPF II Fast progression Alive
11 F 56 IPF I Slow progression Alive
12 F 69 IPF II Slow progression Alive, stable disease
13 F 69 IPF I Slow progression Alive, stable disease
14 F 58 IPF I Slow progression Alive, stable disease
15 F 62 IPF II Slow progression Alive, stable disease
16 M 60 IPF I Slow progression Alive, stable disease
17 F 60 IPF I Slow progression Alive, stable disease
18 F 80 IPF I Slow progression Alive, stable disease
19 F 54 IPF I Fast progression Alive
20 F 42 IPF II Fast progression Died, Ac. exacerbation
21 F 83 IPF II Slow progression Alive
22 F 85 IPF II Slow progression Alive, stable disease
23 M 69 IPF III Slow progression Alive, stable disease

IPF, idiopathic pulmonary fibrosis; Ca, cancer; Ac., acute; CVI, cerebrovascular insult.