TABLE 1

Demographics and baseline characteristics of the 97 patients with newly diagnosed pulmonary arterial hypertension (PAH) initiated with endothelin receptor antagonist and phosphodiesterase type 5 inhibitor dual combination therapy

Male/female34 (35)/63 (65)
Age years54.1±16.5
Body mass index kg·m−227.5±6.6
 >30 kg·m−228 (29)
PAH diagnosis, n (%)
 Idiopathic PAH52 (54)
 Heritable PAH15 (15)
 Anorexigen-induced PAH7 (7)
 PAH-CTD12 (12)
 Portopulmonary hypertension9 (9)
 Repaired PAH-CHD1 (1)
 PAH-HIV1 (1)
NYHA FC
 II15 (15)
 III70 (72)
 IV12 (12)
Clinical signs of right heart failure49 (51)
6-min walk distance m324±132
Borg dyspnoea index4.3±2.0
BNP# ng·L−1 median (IQR)372 (115–710)
  • Data are presented as n (%) or mean±sd, unless otherwise stated. CTD: connective tissue disease; CHD: congenital heart disease; NYHA FC: New York Heart Association functional class; BNP: brain natriuretic peptide; IQR: interquartile range. #: n=42.