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. 2012 Apr 5;142(4):885–892. doi: 10.1378/chest.11-2016

Table 1.

—Subject Characteristics

Characteristic Total (N = 60) Flight Participants (n = 34) Survey-Only Participants (n = 26)
Age, y 50 ± 13 49 ± 11 51 ± 14
Sex
 Female 48 (80) 28 (82) 20 (77)
Race/ethnicity
 White, non-Hispanic 47 (78) 30 (88) 17 (65)
 Black 4 (7) 1 (3) 3 (11)
 Hispanic 4 (7) 1 (3) 3 (11)
 Asian 3 (5) 2 (6) 1 (4)
 Other 2 (3) 0 (0) 2 (8)
Cause of pulmonary hypertension
 Idiopathic/heritable pulmonary arterial hypertension 36 (60) 21 (62) 15 (58)
 Associated pulmonary arterial hypertension
  Connective tissue disease 10 (17) 6 (18) 4 (15)
  Portal hypertension 1 (2) 1 (3) 0 (0)
  Congenital heart disease 3 (5) 0 (0) 3 (11)
  Drug induced 1 (2) 1 (3) 0 (0)
  Other/unsure 4 (7) 2 (6) 2 (8)
 Chronic thromboembolic pulmonary hypertension 5 (8) 3 (9) 2 (8)
WHO functional class
 Class I 5 (8) 2 (6) 3 (11)
 Class II 30 (50) 16 (47) 14 (54)
 Class III 24 (40) 15 (44) 9 (35)
 Class IV 1 (2) 1 (3) 0 (0)
Clinical dataa
 6-min walk distance (n = 21), m 453 ± 115
 Estimated RVSP by echocardiogram (n = 22), mm Hg 72 ± 42
 MPAP by right-sided heart catheterization (n = 19), mm Hg 49 ± 15
Pulmonary hypertension therapyb
 IV/SQ prostacyclin 16 (27) 11 (32) 5 (19)
 Inhaled prostacyclin 6 (10) 5 (15) 1 (4)
 Endothelin receptor antagonist 27 (46) 16 (47) 11 (44)
 Phosphodiesterase-5 inhibitor 36 (61) 21 (62) 15 (60)
Combination therapy (≥ 2 classes) 30 (51) 20 (59) 10 (40)

Data are presented as No. (%) or mean ± SD. MPAP = mean pulmonary artery pressure; RVSP = right-sided ventricular systolic pressure; SQ = subcutaneous; WHO = World Health Organization.

a

Abstracted from subjects’ medical records.

b

Not reported for one subject.

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