PHT (n=15) | Controls (n=11) | p Value | |
---|---|---|---|
Age, years | 61±12 | 51±21 | 0.20 |
Male, n | 6 | 7 | 0.43 |
BMI, kg/m2 | 29±6 | 26±7 | 0.31 |
Aetiology | PAH:10 (IPAH: 8, CTD-PAH:2) CTEPH:5 | ||
Invasive haemodynamics* | |||
sPAP, mm Hg | 65±17 | ||
dPAP, mm Hg | 23±8 | ||
mPAP, mm Hg | 40±10 | ||
PCWP, mm Hg | 10±3 | ||
RAP, mm Hg | 7±5 | ||
Echocardiographic parameters | |||
sPAP, mm Hg | 72±23 | ||
TAPSE, cm | 1.8±0.4 | ||
Right atrial area, cm2 | 26±8 | ||
Pericardial effusion, % | 13% | ||
Lung function parameters | |||
FEV1, % predicted | 87±13 | ||
FVC, % predicted | 97±13 | ||
FEV1/FVC ratio | 73±7 | ||
DLCO, % predicted | 61±14 | ||
TLC, % predicted | 96±10 | ||
Functional capacity | |||
6 min walk distance, m | 429±137 | ||
WHO functional class, n | I: 1 II: 6 III: 8 | ||
Therapy | |||
Endothelin antagonists | 73% | ||
Phosphodiesteriase-5 inhibitors | 53% | ||
Prostanoids | 13% | ||
Combination therapy | 40% |
*Pulmonary haemodynamics are from right heart catheterisation at time of initial diagnosis.
BMI, body mass index; CTD-PAH, connective tissue associated PAH; CTEPH, chronic thromboembolic pulmonary hypertension; DLCO, diffusing capacity for carbon monoxide; dPAP, diastolic pulmonary artery pressure; FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity; IPAH, idiopathic pulmonary arterial hypertension; mPAP, mean pulmonary artery pressure; PAH, pulmonary arterial hypertension; PCWP, pulmonary capillary wedge pressure; PHT, pulmonary hypertension; RAP, right atrial pressure; sPAP, systolic pulmonary artery pressure; TAPSE, tricuspid annular plane systolic excursion; TLC, total lung capacity.