Hemodynamic evaluation of biomaterial-based surgery for Tetralogy of Fallot using a biorobotic heart, in silico, and ovine models

Author:

Singh Manisha1ORCID,Roubertie François23ORCID,Ozturk Caglar1ORCID,Borchiellini Paul4,Rames Adeline4ORCID,Bonnemain Jean15ORCID,Gollob Samuel Dutra6ORCID,Wang Sophie X.17ORCID,Naulin Jérôme2ORCID,El Hamrani Dounia2ORCID,Dugot-Senant Nathalie8,Gosselin Isalyne8,Grenet Célia4,L’Heureux Nicolas4ORCID,Roche Ellen T.16ORCID,Kawecki Fabien4ORCID

Affiliation:

1. Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.

2. IHU Liryc, Electrophysiology and Heart Modeling Institute, F-33604 Pessac, France.

3. Congenital Heart Diseases Department, CHU de Bordeaux, F-33604 Pessac, France.

4. University of Bordeaux, INSERM, BioTis, U1026, F-33000 Bordeaux, France.

5. Department of Adult Intensive Care Medicine, Lausanne University Hospital and University of Lausanne, CH-1011 Lausanne, Switzerland.

6. Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

7. Department of Surgery, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.

8. Plateforme d’histopathologie, TBMcore INSERM US005–CNRS 3427, F-33000 Bordeaux, France.

Abstract

Tetralogy of Fallot is a congenital heart disease affecting newborns and involves stenosis of the right ventricular outflow tract (RVOT). Surgical correction often widens the RVOT with a transannular enlargement patch, but this causes issues including pulmonary valve insufficiency and progressive right ventricle failure. A monocusp valve can prevent pulmonary regurgitation; however, valve failure resulting from factors including leaflet design, morphology, and immune response can occur, ultimately resulting in pulmonary insufficiency. A multimodal platform to quantitatively evaluate the effect of shape, size, and material on clinical outcomes could optimize monocusp design. This study introduces a benchtop soft biorobotic heart model, a computational fluid model of the RVOT, and a monocusp valve made from an entirely biological cell-assembled extracellular matrix (CAM) to tackle the multifaceted issue of monocusp failure. The hydrodynamic and mechanical performance of RVOT repair strategies was assessed in biorobotic and computational platforms. The monocusp valve design was validated in vivo in ovine models through echocardiography, cardiac magnetic resonance, and catheterization. These models supported assessment of surgical feasibility, handling, suturability, and hemodynamic and mechanical monocusp capabilities. The CAM-based monocusp offered a competent pulmonary valve with regurgitation of 4.6 ± 0.9% and a transvalvular pressure gradient of 4.3 ± 1.4 millimeters of mercury after 7 days of implantation in sheep. The biorobotic heart model, in silico analysis, and in vivo RVOT modeling allowed iteration in monocusp design not now feasible in a clinical environment and will support future surgical testing of biomaterials for complex congenital heart malformations.

Publisher

American Association for the Advancement of Science (AAAS)

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