Inferring left atrial stasis and flow from patient-specific 4D contrast dynamics -- physics-informed neural networks with hard constraints vs. indicator dilution theory

ORAL

Abstract

Atrial fibrillation (AF) is the most common cardiac arrhythmia, characterized by irregular left atrial (LA) contractions that impair blood flow and promote stasis, particularly in the left atrial appendage (LAA), increasing thrombosis risk. AF affects nearly one in three individuals over their lifetime and increases the ischemic stroke risk fivefold; it is estimated to be responsible for one third of all strokes. Current risk stratification methods lack patient-specific precision and offer moderate predictive accuracy, particularly in cases where the benefits of anticoagulation therapy are unclear.

Patient-specific computational fluid dynamics (CFD) has shown promise in predicting LAA blood stasis. However, CFD analysis requires high-quality segmentation and meshing of the left atrium and appendage --tasks that remain challenging to automate -- and is sensitive to modeling assumptions such as inflow boundary conditions and blood rheology. This study investigates an alternative approach: using a physics-informed neural network (PINN) to infer LAA flow and stasis directly from the 4D spatiotemporal dynamics of a contrast agent imaged over multiple heartbeats, thereby eliminating the need for LA segmentation and explicit specification of inflow or rheological parameters.

The underlying physical models in our method consist of Navier-Stokes, continuity, a contrast transport equation, and a residence time equation. We incorporated hard constraints in the PINN architecture to enforce initial conditions on residence time and ensure temporal periodicity. We validated PINN predictions for flow velocity and residence time using data from patient-specific CFD simulations as ground-truth data. We also compare these predictions with those obtained by a simplified compartment model of indicator dilution that fits the contrast profile at each image voxel by a gamma-variate function and approximates residence time as the first-order moment of the gamma-variate.

*PREFI-CM and Santander, Spain; NIH (1R01HL160024 and 1R01HL158667); Medtronic; American Heart Association (25CSA1421482).

Presenters

  • Bahetihazi Maidu

    • University of Washington

Authors

  • Bahetihazi Maidu

    • University of Washington
  • Alejandro Gonzalo

    • University of Washington
  • Manuel Guerrero-Hurtado

    • Universidad Carlos III de Madrid
  • Clarissa Bargellini

    • University of Washington
  • Pablo Martinez-Legazpi

    • Universidad Nacional de Educación a Distancia
    • Universidad Nacional de Educación a Distancia & CIBERCV
  • Javier Bermejo

    • Hospital General Universitario Gregorio Marañón
    • Hospital General Universitario Gregorio Marañón & CIBERCV
  • Oscar Flores

    • University Carlos III De Madrid
  • Manuel García-Villalba

    • TU Wien
    • Technical University of Vienna
  • Elliot McVeigh

    • University of California San Diego
  • Andrew M Kahn

    • University of California San Diego
  • Juan C del Alamo

    • Department of Mechanical Engineering, University of Washington, Seattle, Washington; Center for Cardiovascular Biology, University of Washington, Seattle, Washington
    • University of Washington