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. 2014 Oct 16;147(2):484–494. doi: 10.1378/chest.14-1004

TABLE 2 ] .

Clinical Characteristics at Enrollment for All Patients and by Prostacyclin History

Characteristics All Patients (N = 336) Parenteral-Naive (n = 147)a Parenteral-Transitioned (n = 189)b
Specialty of diagnosing physician
 Pulmonologist 222 (66.1) 101 (68.7) 121 (64.0)
 Cardiologist 96 (28.6) 37 (25.2) 59 (31.2)
 Other 18 (5.4) 9 (6.1) 9 (4.8)
PAH duration in y 4.7 ± 4.9 3.1 ± 4.5 5.9 ± 4.9
NYHA functional class at enrollment
 Class I 14 (4.2) 2 (1.4) 12 (6.3)
 Class II 85 (25.3) 24 (16.3) 61 (32.3)
 Class III 169 (50.3) 93 (63.3) 76 (40.2)
 Class IV 38 (11.3) 23 (15.6) 15 (7.9)
 Unknown 30 (8.9) 5 (3.4) 25 (13.2)
6MWD, m, mean ± SD 334.6 ± 128.0 308.2 ± 113.4 350.5 ± 133.8
Hemodynamic parameters
 RAP, mm Hg n = 259 n = 112 n = 147
11.9 ± 7.0 13.6 ± 7.0 10.7 ± 6.7
 mPAP, mm Hg n = 275 n = 123 n = 152
52.9 ± 14.3 54.8 ± 13.1 51.4 ± 15.1
 PCWP, mm Hg n = 266 n = 116 n = 150
11.5 ± 5.6 12.0 ± 6.2 11.1 ± 5.2
 Cardiac index, L/min/m2 n = 242 n = 105 n = 137
2.5 ± 1.0 2.3 ± 0.8 2.7 ± 1.1
 Svo2, % n = 59 n = 24 n = 35
61.8 ± 11.8 60.9 ± 11.3 62.5 ± 12.2
 PVRI, Wood units × m2 n = 225 n = 99 n = 126
19.7 ± 12.3 21.7 ± 12.0 18.0 ± 12.4
Concomitant PAH medications, at RTS-Epo start
 PDE5i without ERA 82 (24.4) 32 (21.8) 50 (26.5)
 ERA without PDE5i 49 (14.6) 21 (14.3) 28 (14.8)
 PDE5i + ERA 81 (24.1) 37 (25.2) 44 (23.3)
 Neither 124 (36.9) 57 (38.8) 67 (35.4)
Initial dose of RTS-Epoc n = 316 n = 127 n = 189
 Median 16.0 2.0 29.0

Data are given as mean ± SD or No. (%). 6MWD = 6-min walk distance; ERA = endothelial receptor antagonist; mPAP = mean pulmonary arterial pressure; NYHA = New York Heart Association; PDE5i = type 5 phosphodiesterase inhibitor; PAH = pulmonary arterial hypertension; PCWP = pulmonary capillary wedge pressure; PVRI = pulmonary vascular resistance index (Wood units × m2); RAP = right arterial pressure; RTS-Epo = room temperature stable-epoprostenol; Svo2 = venous oxygen saturation.

a

Includes n = 119 patients who were prostacyclin-naive, n = 26 patients who transitioned from an inhaled prostacyclin, and n = 2 patients who transitioned from an oral prostacyclin at study entry.

b

Includes n = 180 patients who transitioned from epoprostenol and n = 9 patients who transitioned from treprostinil at study entry.

c

The initial dose at time of initiation of prolonged RTS-Epo, which may not be at enrollment.