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Table 1 Characteristics of CTEPH subjects of different severity

From: Cardiopulmonary exercise testing and pulmonary function testing for predicting the severity of CTEPH

Variables

Total

Mild

Moderate

Severe

P

Clinical characteristics

Age (years)

61.2 ± 11.2

65.5 ± 9.9

59.8 ± 9.3

60.4 ± 12.0

0.418

Sex, n (female/male)

31/24

4/6

7/3

20/15

0.396

Height (m)

1.6 ± 0.1

1.7 ± 0.1

1.6 ± 0.1

1.6 ± 0.1

0.527

Weight (kg)

63.3 ± 12.9

65.3 ± 12.0

56.4 ± 12.1

64.7 ± 13.1

0.178

Body mass index (kg/m2)

23.6 ± 3.2

23.6 ± 2.9

20.8 ± 3.3

24.4 ± 2.9

0.016

WHO classification II/III/IV, n

15/39/1

6/4/0

3/6/1

6/29/0

0.017

Blood test

NT-proBNP (pg/mL)

809.0 (296.9,2284.0)

143.0 (63.8,286.7)

648.5 (266.3,2049.0)

1082.0 (642.0,2674.0)

0.001

Right heart catheterization parameters

PAP (mm Hg)

48.3 ± 13.2

28.6 ± 3.3

39.5 ± 3.9

56.4 ± 8.0

< 0.001

PAWP (mm Hg)

7.0 (4.0,9.0)

8.5 (5.5,10.3)

4.0 (3.0,9.3)

7.0 (4.0,9.0)

0.250

CO (L/min)

5.0 ± 1.4

5.8 ± 1.7

4.8 ± 1.4

4.9 ± 1.3

0.221

CI (L/min/m2)

3.0 ± 0.8

3.3 ± 0.8

3.0 ± 0.7

2.9 ± 0.7

0.283

PVR (wood u)

9.0 ± 4.2

3.7 ± 1.3

7.6 ± 2.4

10.9 ± 3.8

0.011

RAP (mm Hg)

3.0 (1.0,6.0)

0.5 (0,4.5)

1.0 (0,1.3)

4.0 (2.0,7.0)

0.001

Pulmonary function testing parameters

FVC (L)

2.7 ± 0.9

2.8 ± 0.8

2.8 ± 1.1

2.6 ± 0.8

0.790

FVC (% Pred)

84.4 ± 15.8

88. 8 ± 15.6

86.3 ± 24.9

82.6 ± 12.5

0.508

FEV1 (L)

2.1 ± 0.7

2.2 ± 0.5

2.2 ± 0.8

2.0 ± 0.7

0.488

FEV1 (% Pred)

79.5 ± 17.1

85.7 ± 14.0

87.0 ± 23.9

75.6 ± 14.7

0.076

FEV1/FVC (%)

75.9 ± 8.8

78.8 ± 9.3

81.7 ± 8.0

73.4 ± 8.0

0.041

RV (L)

2.4 ± 0.7

2.5 ± 0.9

2.6 ± 0.3

2.3 ± 0.7

0.562

RV (% Pred)

126.8 ± 34.3

122.6 ± 46.1

134.9 ± 27.4

125.7 ± 32.9

0.700

TLC (L)

5.1 ± 1.3

5.3 ± 1.5

5.4 ± 1.2

5.0 ± 1.3

0.629

TLC (% Pred)

100.6 ± 19.0

101.7 ± 26.0

104.7 ± 15.4

99.1 ± 18.0

0.698

RV/TLC (%)

47.3 (41.8,53.8)

48.3 (39.0,53.8)

49.0 (39.4,61.0)

47.2 (42.0,56.1)

0.910

SB DLCO (% Pred)

81.8 ± 19.2

81.4 ± 25.2

85.0 ± 28.7

81.0 ± 14.0

0.843

Specific medications

PDE-5 inhibitors (n, %)

38 (69.1%)

9 (90.0%)

5 (50.0%)

24 (68.6%)

0.153

ERAs (n, %)

33 (60.0%)

0

7 (70.0%)

26 (74.3%)

0.000

Prostacyclin analogs (n, %)

1 (1.8%)

1 (10.0%)

0

0

0.101

sGC activators

3 (5.5%)

0

0

3 (8.6%)

0.404

Combination (n, %)

20 (36.4%)

0

2 (20.0%)

18 (51.4%)

0.006

  1. Range for “Mild”: 35 > PAP (mm Hg) ≥ 25; range for “Moderate”: 45 > PAP (mm Hg) ≥ 35; range for “Severe”: PAP (mm Hg) ≥ 45. The data are presented as mean ± SD, median (interquartile range), or n. Statistical analysis of characteristics of “Mild”, “Moderate” and “Severe” was analyzed with One-way ANOVA test, Kruskal–Wallis test or chi-square test, and was presented as “P”. WHO = World Health Organization; BNP = brain natriuretic peptide; PAP = pulmonary artery pressure; PAWP = pulmonary arterial wedge pressure; CO = cardiac output; CI = cardiac index; PVR = pulmonary vascular resistance; RAP = right atrial pressure; FVC = forced vital capacity; FEV1 = forced expiratory volume in 1 s; RV = residual volume; TLC = total lung capacity; SB DLCO = carbon monoxide diffusing capacity; PDE-5 inhibitors = phosphodiesterase type 5 inhibitors; ERAs = endothelial receptor antagonists; sGC activators = soluble guanylate cyclase activators