Multiscale modelling of reversed Potts shunt as a potential palliative treatment for suprasystemic idiopathic pulmonary artery hypertension in children

TL;DR

This study develops a patient-specific multiscale model of the reversed Potts shunt in pediatric pulmonary hypertension, providing insights into haemodynamics and aiding clinical decision-making for this complex treatment.

Contribution

The paper introduces a novel multiscale modelling approach for patient-specific haemodynamics of reversed Potts shunt in children with pulmonary hypertension.

Findings

Reversed Potts shunt equalizes aortic and PA pressures.

Increasing PS diameter decreases Qp/Qs ratio linearly.

Model predicts haemodynamic changes post-surgery accurately.

Abstract

Reversed Potts shunt (PS) was suggested as palliation for patients with suprasystemic pulmonary arterial hypertension (PAH) and right ventricular (RV) failure. PS, however, can result in poorly understood mortality. Here, a patient-specific geometrical multiscale model of PAH physiology and PS is developed for a paediatric PAH patient with stent-based PS. In the model, 7.6mm-diameter PS produces near-equalisation of the aortic and PA pressures and Qp/Qs (oxygenated vs deoxygenated blood flow) ratio of 0.72 associated with a 16% decrease of left ventricular (LV) output and 18% increase of RV output. The flow from LV to aortic arch branches increases by 16%, while LV contribution to the lower body flow decreases by 29%. Total flow in the descending aorta (DAo) increases by 18% due to RV contribution through the PS with flow into the distal PA branches decreasing. PS induces 18% increase of RV work due to its larger stroke volume pumped against lower afterload. Nonetheless, larger RV work does not lead to increased RV end-diastolic volume. Three-dimensional flow assessment demonstrates the PS jet impinging with a high velocity and wall shear stress on the opposite DAo wall with the most of the shunt flow being diverted to the DAo. Increasing the PS diameter from 5mm up to 10mm results in nearly linear decrease in post-operative Qp/Qs ratio. In conclusion, this model reasonably represents patient-specific haemodynamics pre- and post-creation of the PS, providing insights into physiology of this complex condition, and presents a predictive tool that could be useful for clinical decision-making regarding suitability for reversed PS in PAH patients with drug-resistant suprasystemic PAH.