Computational models of aortic coarctation in hypoplastic left heart syndrome: considerations on validation of a

Giovanni Biglino1, Chiara Corsini, Silvia Schievano

  • 1* These authors contributed equally to this work.

Insights

This study validates a computational model for hypoplastic left heart syndrome with aortic coarctation using physical data. The validated model reliably predicts hemodynamic information for complex congenital heart disease investigations.

Area of Science:

  • Cardiovascular research
  • Computational fluid dynamics
  • Medical device simulation

Background:

  • Computational models require validation against physical data for reliable cardiovascular research.
  • Complex congenital heart disease, such as hypoplastic left heart syndrome with aortic coarctation, presents unique modeling challenges.

Purpose of the Study:

  • To experimentally validate a patient-specific computational model of surgically palliated hypoplastic left heart syndrome with aortic coarctation.
  • To demonstrate the reliability of extrapolating hemodynamic information from validated computational models for clinical use.

Main Methods:

  • A multi-scale approach combining a 3D patient-specific aortic arch model with a lumped parameter network (LPN) was used.
  • The model simulated a modified Blalock-Taussig shunt and aortic coarctation under various flow regimes.
  • Experimental data from a mock circulatory system were used for in silico model validation, assessing viscosity impacts.

Main Results:

  • Computational and experimental results showed good agreement in flow and pressure waveforms (e.g., mean aortic pressure within 4.8% difference).
  • The validated numerical approach proved reliable for simulating complex congenital heart disease hemodynamics.
  • Fluid viscosity and turbulence models had minimal impact on key hemodynamic parameters.

Conclusions:

  • Methodological insights were provided for integrating experimental data into computational models.
  • A multi-scale approach is effective for simulating complex congenital cardiovascular physiology.
  • Validated computational models offer reliable hemodynamic insights for clinical investigations.
Abstract

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