Abstract

Around 8% of all newborns with a Congenital Heart Defect (CHD) have only a single functioning ventricle. The Fontan operation has served as palliation for this anomaly for decades, but the surgery entails multiple complications, and the survival rate is less than 50% by adulthood. A rapidly testable novel alternative is proposed by creating a bifurcating graft, or Injection Jet Shunt (IJS), used to “entrain” the pulmonary flow and thus provide assistance while reducing the caval pressure. A dynamically scaled Mock Flow Loop (MFL) has been configured to validate this hypothesis. Three IJS nozzles of varying diameters 2, 3, and 4 mm with three aortic anastomosis angles and pulmonary vascular resistance (PVR) reduction have been tested to validate the hypothesis and optimize the caval pressure reduction. The MFL is based on a Lumped-Parameter Model (LPM) of a non-fenestrated Fontan circulation. The best outcome was achieved with the experimental testing of a 3 mm IJS by producing an average caval pressure reduction of more than 5 mmHg while maintaining the clinically acceptable pulmonary flow rate (Qp) to systemic flow rate (Qs) ratio of ~1.5. Furthermore, alteration of the PVR helped in achieving higher caval pressure reduction with the 3 mm IJS at the expense of an increase in Qp/Qs ratio.

Highlights

  • A structurally normal heart consists of two separate pumping chambers or ventricles: one ventricle pumps “de-oxygenated” blood returning from the body to the lungs, and the other pumps oxygenated blood to the body

  • A parametric study on Injection Jet Shunt (IJS) nozzle aortic anastomosis angles, and pulmonary vascular resistance (PVR) effect have been conducted in these experiments

  • The diameter, IJS aortic anastomosis angles, and PVR effect have been conducted in these excomparative study on the IJS nozzle shows that the 3 mm nozzle is the most efficient for periments

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Summary

Introduction

A structurally normal heart consists of two separate pumping chambers or ventricles: one ventricle pumps “de-oxygenated” blood returning from the body to the lungs, and the other pumps oxygenated blood to the body. 1 in 3841 babies is born with hypoplastic left heart syndrome (HLHS). A subset of HLHS is a rare congenital heart defect in which the left ventricle is underdeveloped [1,2,3]. The remaining viable right ventricle must support both systemic and pulmonary circulations, becoming overloaded [4,5]. These patients do not survive unless a series of palliative operations are performed to establish an adequate flow to both the lungs and body. The Fontan operation has served as palliation for this anomaly for decades, but multiple complications often result in chronic illness, a severe reduction in quality of life, and survival rates of less than

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