Table 2.

Characteristics of patients with idiopathic pulmonary arterial hypertension (IPAH).

CharacteristicsUnmatched, n = 155Matched, n = 66Absolute Standardized Difference
No Warfarin, n = 64Warfarin, n = 91No Warfarin, n = 33Warfarin, n = 33Unmatched n = 155Matched n = 66
Female sex, n (%)42 (66)66 (73)20 (61)21 (64)0.120.05
PAH characteristics at diagnosis
  mPAP mm Hg, mean (SD)52.9 (13.5)42.6 (13.3)51.6 (15.6)47.5 (15.9)0.770.26
  WHO Functional Class III/IV29 (45)54 (59)18 (55)18 (55)0.200
  Moderate-severe RV enlargement1 (2)16 (18)1 (3)4 (12)0.170.09
  Moderate-severe RV hypokinesis19 (30)50 (55)13 (39)17 (52)0.330.16
Comorbidities, n (%)
  Cancer3 (5)10 (11)3 (9)1 (3)0.070.06
  Coronary artery disease8 (13)16 (18)4 (12)1 (3)0.060.09
  Diabetes mellitus14 (22)15 (16)9 (27)7 (21)0.070.02
  Hyperlipidemia8 (13)7 (8)3 (9)1 (3)0.050.06
  Hypertension24 (38)24 (26)10 (30)11 (33)0.130.04
  Peripheral vascular disease1 (2)1 (1)000.010
  Ischemic stroke2 (3)8 (9)1 (3)2 (6)0.060.03
Concomitant medications
  Calcium channel blocker12 (19)33 (36)11 (33)12 (36)0.210.04
  ER antagonist11 (17)43 (47)9 (27)8 (24)0.370.04
  PDE inhibitor12 (19)24 (26)9 (27)8 (24)0.090.04
  Prostaglandin analog3 (5)24 (26)1 (3)4 (12)0.240.09
  • mPAP: mean pulmonary artery pressure; RV: right ventricular; WHO: World Health Organization; RV: right ventricular; ER: endothelin receptor; PDE: phosphodiesterase.