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Table 2 Comparisons among pulmonologist and non-pulmonologist physicians, according to progressionassessment of disease

From: Management and attitudes about IPF (Idiopathic Pulmonary Fibrosis) among physicians from Latin America

Treatment

Pulmonologist

 

Yes

N = 91 (29.7%)

No

N = 215 (70.3%)

 

Total

 
 

n

%

n

%

OR (CI 95%)

n

%

p value*

Supplemental oxygen

77

84.6

141

65.6

2.89 (1.53–5.45)

218

71.2

0.001

Corticosteroids (CS)

39

42.9

108

50.2

0.74 (0.45–1.22)

147

48.0

0.238

Azatioprine

5

5.5

13

6.0

0.90 (0.31–2.61)

18

5.9

0.851

CS + immunosupressors (IS)

6

6.6

26

12.1

0.51 (0.20–1.29)

32

10.5

0.151

N-acetylcisteine (NAC)

30

33.0

59

27.4

1.30 (0.77–2.21)

89

29.1

0.331

Corticosteroids + NAC + IS

14

15.4

45

20.9

0.69 (0.36–1.33)

59

19.3

0.261

Corticosteroids + NAC

17

18.7

46

21.4

0.84 (0.45–1.57)

63

20.6

0.591

Colchicine

3

3.3

11

5.1

0.63 (0.17–2.32)

14

4.6

0.486

Ciclosporine

0

0.0

2

0.9

NS

2

0.7

0.356

Anti-blotting

1

1.1

15

7.0

0.15 (0.02–1.14)

16

5.2

0.035

Pirfenidona

38

41.8

14

6.5

10.29 (5.20–20.39)

52

17.0

0.000

Pirferidona + NAC

18

19.8

7

3.3

7.33 (2.94–18.25)

25

8.2

0.000

  1. *Chi square