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. 2024 May 24;14(2):e12361. doi: 10.1002/pul2.12361

Table 1.

Patient characteristics for the pulmonary arterial hypertension cohort.

Population (n = 223)
Demographics
Age 48.1 (14.1)
Male 49 (22.0%)
White race 124 (55.6%)
Etiology
Idiopathic 90 (40.4%)
Connective tissue disease 55 (24.7%)
IV drug abuse 7 (3.2%)
Simple repaired congenital 4 (1.8%)
Comorbidity
Lung disease 17 (7.6%)
Advanced liver disease 14 (6.3%)
Medications
Treatment naive 145 (65%)
Biological markers
NT‐proBNP (pg/mL)
<300 59 (26.5%)
300−1100 55 (24.7%)
≥ 1100 109 (48.9%)
GFR by CKDepi (mL/min/1.73 m2) 55.0 (22.1)
Sodium (mM) 138 (3.4)
Hemoglobin (g/dL) 13.3 (2.3)
Bilirubin (mg/dL) 0.97 (1.0)
RHC parameters
mPAP (mmHg) 51.6 (13.8)
RAP (mmHg) 9.3 (5.2)
PAWP (mmHg) 11.1 (4.8)
CI (L/min/m2) 2.0 (0.6)
PVRi (WU/m2) 22.5 (6.3)
NYHA status
1 6 (2.7%)
2 52 (23.3%)
3 80 (35.9%)
4 78 (35.0%)
Reveal lite 2.0 score
≤5 53 (23.8%)
6−7 42 (18.8%)
≥8 127 (57%)
Outcomes
Death or transplant within 5 years 78 (35%)

Abbreviations: GFR, glomerular filtration rate; mPAP, mean pulmonary artery pressure; NYHA, New York Heart Association; PAWP, pulmonary capillary wedge pressure; PVRi, pulmonary vascular resistance index; RAP, right atrial pressure; RHC, right heart catheterization.