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Table 1 Demographics, classification and treatment variables

From: Risk stratification and prognostic factors in patients with pulmonary arterial hypertension and comorbidities a cross-sectional cohort study with survival follow-up

Characteristics

Complete dataset

(n = 142)

PAH

(n = 90)

PAH with comorbidities

(n = 52)

p-value

n (%)

n (%)

n (%)

Female sex no. [%]

87 (61.3)

66 (73.3%)

21 (40.4%)

< 0.0001

Diagnostic group of PAH [%]

 IPAH

44 (31%)

44 (48.8%)

  

 HPAH

4 (2.8%)

4 (4.4%)

  

 DPAH

1 (0.7%)

1 (1.1%)

  

 APAH

41 (28.9%)

41 (45.6%)

  

 PAH with cardiac comorbidities

33 (23.3%)

 

33 (63.5%)

 

 PAH with pulmonary comorbidities

19 (13.4%)

 

19 (36.5%)

 

Group of APAH [%]

 Connective tissue diseases

37 (26.1%)

37 (41.1%)

  

 HIV

1 (2.5%)

1 (1.1%)

  

 Portal hypertension

3 (0.7%)

3 (3.3%)

  

No. of PAH drugs

   

0.82

 Monotherapy

90 (63.4%)

56 (62.2%)

34 (65.4%)

 

 Double combination

50 (35.2%)

33 (36.7%)

17 (32.7%)

 

 Triple combination

2 (1.4%)

1 (1.1%)

1 (1.9%)

 

Type of PAH drug at diagnosis [%]

   

0.02

 Calcium channel blocker

12 (8.5%)

4 (4.4%)

8 (15.4%)

 

 Endothelin receptor antagonist

62 (43.7%)

48 (53.3%)

14 (26.9%)

 

 Phosphodiesterase 5 inhibitor

108 (76.1%)

65 (72.2%)

43 (82.7%)

 

 Prostacyclin

2 (1.4%)

1 (1.1%)

1 (1.9%)

 

 Soluble guanylate cyclase stimulator

7 (4.9%)

3 (3.3%)

4 (7.7%)

 

Oxygen treatment

53 (37.3%)

25 (27.8%)

28 (53.8%)

 

Anticoagulants

116 (81.7%)

69 (76.7%)

47 (90.4%)

0.042

Diuretics

108 (76.1%)

63 (70.0%)

45 (86.5%)

0.026

  1. In case of missing data, sample sizes are given in the column of n. sample size is given in case of missing values. IPAH idiopathic pulmonary arterial hypertension, HPAH heritable pulmonary arterial hypertension, DPAH drug-induced pulmonary arterial hypertension, APAH associated pulmonary arterial hypertension, PAH pulmonary arterial hypertension