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. 2024 Jan 15;11(3):1540–1552. doi: 10.1002/ehf2.14611

Table 1.

Demographics, patient baseline characteristics, co‐morbidities, and cardiovascular risk factors in 50 patients with newly diagnosed pulmonary arterial hypertension (PAH) undergoing rapid sequential combination therapy

All (n = 50) Classical PAH (n = 37) PAH with co‐morbidities (n = 13) P‐value
Patient characteristics
Age, years (means ± SD) 54.5 ± 18.9 49.8 ± 18.9 67.8 ± 10.7 <0.001
Age, years (median, Q1–Q3) 57 (42–71) 50 (30–68) 68 (65–76) <0.001
Gender, m/f (%) 34/66 30/70 46/54 0.3219
Type of PAH:
Idiopathic, n (%) 38 (76.0%) 27 (73.0%) 11 (84.6%) 0.480
Hereditary, n (%) 2 (4.0%) 2 (5.1%) 0 (0.0%) 1
Drug‐induced, n (%) 2 (4.0%) 1 (2.6%) 1 (9.1%) 0.456
Connective tissue disease, n (%) 7 (14.0%) 6 (15.4%) 1 (9.1%) 0.660
Congenital heart disease, n (%) 0 (0.0%) 0 (0.0%) 0 (0.0%) 1
HIV, n (%) 1 (2.0%) 1 (2.6%) 0 (0.0%) 1
Other, n (%) 0 (0.0%) 0 (0.0%) 0 (0.0%) 1
Co‐morbidities/CV risk factors
Hypertension, n (%) 29 (58.0%) 17 (46.0%) 12 (92.3%) 0.004
Diabetes, n (%) 12 (24.0%) 3 (8.1%) 9 (69.2%) <0.001
Dyslipidaemia, n (%) 9 (18.0%) 3 (8.1%) 6 (46.2%) 0.006
CAD, n (%) 7 (14.0%) 2 (5.4%) 5 (38.5%) 0.009
BMI > 30 kg/m2, n (%) 17 (34.0%) 8 (20.5%) 9 (69.2%) 0.005

Distributions of qualitative variables were compared by the Fisher's exact test.

BMI, body mass index; CAD, coronary artery disease; CV, cardiovascular; PAH, pulmonary arterial hypertension.