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. 2014 May 28;14:91. doi: 10.1186/1471-2466-14-91

Table 1.

Comparison between idiopathic pleuroparenchymal fibroelastosis (IPPFE) and idiopathic pulmonary fibrosis (IPF): clinical characteristics

  IPPFE (n = 6) IPF (n = 28) p value
Sex, male/female
5/1
26/2
0.452*
Age at biopsy, yr
69.2 ± 3.9
61.4 ± 9.9
0.072
Smoking history, current/ex/never
0/3/3
13/13/2
0.011*
Pack-year of smoking
29.3 ± 33.1
66.8 ± 97.4
0.363
Detection by medical check-up, n (%)
3 (50)
21 (75.0)
0.328*
Respiratory symptoms at biopsy, n (%)
6 (100)
19 (67.9)
0.162*
Body mass index, kg/m2
17.9 ± 0.9
24.3 ± 2.8
<0.0001
Clubbing of finger, n (%)
1 (16.7)
6 (21.4)
0.999*
Fine crackles, n (%)
3 (50)
27 (96.4)
0.012*
Pneumothorax, n (%)
4 (66.7)
1 (3.6)
0.002*
Acute exacerbation, n (%)
1 (16.7)
6 (21.4)
0.999*
Therapeutic intervention, n (%)
4 (66.7)
15 (53.6)
0.672*
Period from detection of IP until acquisition of lung specimens
73.3 ± 46.1
29.7 ± 34.3
0.012
Observation period, mo
39.8 ± 29.2
67.8 ± 46.7
0.206
Death, n (%) 3 (50.0) 12 (42.9) 0.999*

Data are presented as n, mean ± SD or n (%).

Data were analyzed with Student’s t-test or *Fisher’s exact probability test.

Abbreviations: IPPFE idiopathic pleuroparenchymal fibroelastosis, IPF idiopathic pulmonary fibrosis, IP interstitial pneumonia.