A patient-specific lumped-parameter model calibrated to clinical data quantified vessel-specific remodeling and simulated RV pressure-volume dynamics to distinguish among PH phenotypes.
Does a patient-specific lumped-parameter model accurately quantify vessel-specific remodeling and predict right ventricular function across pulmonary hypertension phenotypes?
A novel patient-specific lumped-parameter model calibrated with routine clinical data can noninvasively simulate right ventricular pressure-volume dynamics and distinguish among pulmonary hypertension phenotypes.
Purpose: Pulmonary hypertension (PH) is a heterogeneous disease with patient-specific variability and vessel-specific remodeling, which eventually lead to right ventricular (RV) failure. The gold standard for RV assessment—pressure–volume (PV) loop acquisition—is invasive and limited to specialized settings. This study aims to develop a patient-specific lumped-parameter model that quantifies vessel-specific remodeling and simulates RV PV loops across PH phenotypes using routine clinical data. Methods: A lumped-parameter model was calibrated using right heart catheterization and echocardiography data. Model agreement was assessed by R2 values for pressure and flow goodness-of-fit, and model-derived hemodynamic metrics were comparedwith clinical values. A dimensionality reduction approach was applied to investigate how well different PH phenotypes could be separated. Results: Across the cohort, the lumped-parameter model showed good agreement with clinical data. Model-derived vessel-specific (pulmonary arterial, capillary, venular) parameters highlighted physiological distinctions among phenotypes. PredictedRV PV loops revealed phenotype-specific differences in right ventricular volumes, pressures, and stroke work. The linear discriminant analysis (LDA) demonstrated qualitative separability, indicating that model-derived, nonmeasurable features offer additional discriminatory information. Conclusion: Our results demonstrate that lumped-parameter models can be calibrated to clinical data to quantify vessel-specific remodeling and simulate RV pressure–volume dynamics to provide useful information for distinguishing among different PHphenotypes. This underscores the potential of computational models as noninvasive, clinically feasible tools for assessing in-depth pulmonary vascular and RV function in PH.
Lechuga et al. (Wed,) conducted a other in Pulmonary hypertension. Patient-specific lumped-parameter model was evaluated on Model agreement (R2 values for pressure and flow goodness-of-fit) and separability of PH phenotypes. A patient-specific lumped-parameter model calibrated to clinical data quantified vessel-specific remodeling and simulated RV pressure-volume dynamics to distinguish among PH phenotypes.