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Table 2 Baseline characteristics between the nintedanib group and no antifibrotic therapy group in historical control study

From: Temporal echocardiographic assessment of pulmonary hypertension in idiopathic pulmonary fibrosis patients treated with nintedanib with or without oxygen therapy

 

IPF patients with LTOT (n = 19)

P value

IPF patients without LTOT (n = 12)

P value

Nintedanib

No antifibrotic therapy

Nintedanb

No antifibrotic therapy

(n = 9)

(n = 10)

(n = 7)

(n = 5)

Age (years)

69 [57–77]

72 [60–83]

0.315

73 [64–80]

70 [48–76]

0.639

Male

8 (88%)

6 (60%)

0.153

6 (86%)

4 (80%)

0.793

Weight (kg)

68.7 [43.3–73.9]

54.7 [26.0–72.0]

0.065

59.6 [44.3–61.5]

52.9 [46.9–63.0]

0.876

Body mass index

25.1 [15.1–26.9]

20.2 [13.7–28.8]

0.661

22.0 [19.0–26.7]

20.7 [18.6–26.7]

0.876

Smoking status

 Never / Former / Current smoker

0 / 9 / 0

3 / 7 / 0

0 / 7 / 0

1 / 4 / 0

Time since the diagnosis of IPF (years)

2 [0–9]

1 [0–3]

0.400

4 [1–8]

3 [0–4]

0.202

mMRC dyspnea scale

3 [0–3]

2 [1–3]

0.842

1 [0–2]

2 [0–3]

0.343

GAP score

5 [2–8]

5 [1–7]

0.796

4 [3–5]

5 [2–5]

0.648

SpO2 on room air at rest (%)

95 [94–97]

95 [89–98]

0.573

97 [94–99]

96 [95–98]

0.648

PaO2 on room air at rest (mmHg)

75 [59–94]

70 [47–89]

0.277

88 [81–122]

91 [75–103]

0.927

PASP measured by TTE at baseline (mmHg)

33.0 [21.0–59.0]

41.4 [31–56.2]

0.278

35.0 [27.6–55.3]

37.0 [27.9–56.2]

0.775

Pulmonary function tests

 FVC (mL)

2.140 [1.060–3.030]

1.735 [1.170–2.480]

0.278

1.840 [1.540–2.690]

2.020 [1.060–2.370]

0.953

 FVC (% predicted)

66 [28–88]

61 [46–74]

0.720

57 [51–79]

64 [35–73]

0.530

 FEV1 (mL)

1.990 [1.030–2.407]

1.560 [1.010–2.280]

0.356

1.560 [1.330–2.270]

1.930 [1.050–2.100]

1.000

 FEV1 (% predicted)

67 [34–91]

72 [56–83]

0.549

76 [50–81]

73 [40–85]

0.876

 DLCO (mL/min/mmHg)

8.3 [5.1–13.6]

6.6 [4.3–11.7]

0.091

10.7 [8.1–18.6]

10.0 [7.3–16.3]

0.788

 DLCO (% predicted)

49 [30–76]

40 [29–73]

0.299

70 [48–91]

74 [38–129]

1.000

Radiographic findings

 Pulmonary emphysema

5 (56%)

3 (30%)

0.414

1 (14%)

1 (20%)

0.682

Comorbidity

      

 Hypertension

3 (33%)

4 (40%)

0.764

3 (43%)

1 (20%)

0.408

 Chronic heart failure

0 (0%)

0 (0%)

0 (0%)

0 (0%)

No antifibrotic agent

 No treatment

3 (30%)

1 (20%)

 Corticosteroid monotherapy

1 (10%)

2 (40%)

 Combined corticosteroid and immunomodulator therapy

5 (50%)

2 (40%)

 Inhalation of N-acetyl-cysteine

1 (10%)

0 (0%)

  1. Data are presented as median [range] or number of patients (percentage)
  2. IPF idiopathic pulmonary fibrosis, LTOT long-term oxygen treatment, mMRC modified Medical Research Council, GAP Gender-Age-Physiology, SpO2 arterial oxygen saturation measured by pulse oximetry, PaO2 partial pressure of arterial oxygen, PASP pulmonary artery systolic pressure, TTE transthoracic echocardiography, FVC forced vital capacity, FEV1 forced expiratory volume in 1 s, DLCO diffusing capacity of the lung for carbon monoxide
  3. P value: the nintedanib group vs the no antifibrotic therapy group