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. 2020 May 24;21:127. doi: 10.1186/s12931-020-01393-1

Table 1.

Demographics, classification and treatment variables

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

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