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. 2024 Apr 19;11(4):124. doi: 10.3390/jcdd11040124

Table 1.

Baseline Patient Demographic Data and Functional Parameters of PHPVD versus PHLHD group.

Characteristics PHPVD PHLHD p Value
Total Number of Patients n = 14 n = 10
Female 10 (73.00%) 5 (50.00%) 0.2038
Age (Years) 75 (56–89) 74 (51–88) 0.8739
Nitroprusside Dose (mcg/kg/min) 0.84 ± 0.42 1.22 ± 0.40 0.0126
Comorbidities
HFpEF 9 (64.20%) 9 (90.00%) 0.3408
BMI (kg/m2) 29 (17.77–45.21) 33 (21.45–60.45) 0.4031
CAD 7 (50.00%) 4 (40.00%) 0.6968
HTN 11 (78.60%) 10 (100.00%) 0.2391
DM II 7 (50.00%) 4 (40.00%) 0.6968
Atrial fibrillation/Flutter 6 (42.90%) 7 (70.00%) 0.2397
Lung Disease (COPD/ILD) 8 (57.10%) 4 (40.00%) 0.6802
OSA 6 (42.90%) 5 (50.00%) 0.9999
CKD 7 (50.00%) 1(10.00%) 0.0791
Autoimmune diseases 3 (21.40%) 0 (0%) 0.2391
PH Etiology
Non-PAH † 2
PAH
  Idiopathic-PAH 2
  ILD-PAH 2
  CTD-PAH 2
  Toxin-PAH 1
Medications
ARNi/ACEi/ARB 9 (64.20%) 8 (80.00%) 0.6529
MRA 10 (71.40%) 9 (90.00%) 0.3577
SGLT2i 2 (14.20%) 7 (70.00%) 0.0104
PDE5 inhibitor only 2 (14.20%) 1 (10.00%) >0.9999
Echocardiographic Parameters
Mean ± STDev Mean ± STDev p Value
LVEF 63.46 ± 8.02 59.4 ± 5.91 0.1902
LAVi 37.04 ± 11.12 48.88 ± 31.86 0.4833
Diastolic Dysfunction (Grade I–III) 9 (64.20%) 8 (80.00%) 0.66
IVS Systolic Septal flattening 9 (69.23%) 7 (70.00%) >0.9999
RVEDd (cm)—basal width 4.03 ± 0.52 4.7 ± 0.70 0.0341
RVOT PW doppler notch 9 (69.23%) 10 (100%) 0.1045
RA size (RAVi) 30.60 ± 10.74 50.91 ± 21.56 0.0147
PASP 57.41 ± 16.52 62.77 ±17.18 0.354
TAPSE 1.98 ± 0.62 1.33 ± 0.51 0.031
RV S′ 12.28 ± 2.89 8.97 ± 2.30 0.0054

Notes: For nominal variables n (%), for continuous variables mean (range) standard deviation as applicable. Abbreviation: PHPVD, pulmonary hypertension-pulmonary vascular disease; PHLHD, pulmonary hypertension-left heart disease; HFpEF, heart failure with preserved ejection fraction; BMI, body mass index; CAD, coronary artery disease; HTN, hypertension; DM II, diabetes mellitus type 2; OSA, obstructive sleep apnea; CKD, chronic kidney disease; PAH, pulmonary arterial hypertension; CTD, connective tissue disease; ILD, interstitial lung disease; ARNi, angiotensin receptor/neprilysin inhibitor; ACEi, angiotensin-converting enzyme inhibitor; ARB, angiotensin receptor blocker; MRA, mineralocorticoid receptor antagonists; SGLT2i, sodium–glucose cotransporter-2 inhibitor; PDE5, Phosphodiesterase 5 Inhibitors; LVEF, left ventricular ejection fraction; IVS, interventricular septum; RVEDd, right ventricular end-diastolic diameter; RVOT, right ventricular outflow tract; RA, right atrium; RAVi, right atrial volume index; PASP, pulmonary arterial systolic pressure; TAPSE, tricuspid annular plane systolic excursion; RV S′, Right ventricular peak tricuspid annular systolic tissue velocity. † Non-PAH PH: Defined as combined pre- and postcapillary pulmonary hypertension (cpcPH) with normalization of PCWP with nitroprusside but no clear PAH etiology; this phenotype is distinguished from pulmonary arterial hypertension (PAH) by the presence of a significant postcapillary component, which was characterized during this study (see Figure 1).