Flow transport and not ejection fraction determines blood stasis in patients with impaired left ventricular systolic

Pablo Martinez-Legazpi1, Javier Bermejo2, Juan C Del Alamo3

  • 1Department of Mathematical Physics and Fluids, Facultad de Ciencias, Universidad Nacional de Educación a Distancia, UNED and CIBERCV, Madrid, Spain.

PubMed

Insights

Queue models reveal how blood flow dynamics in the left ventricle (LV) impact thrombosis risk. Reduced ejection fraction (EF) combined with direct flow (DF) significantly increases blood stasis, explaining why EF alone is a poor predictor of intraventricular thrombosis.

Area of Science:

  • Cardiovascular Physiology
  • Biomedical Engineering
  • Medical Imaging Analysis

Background:

  • Impaired left ventricular (LV) systolic function increases risk of intraventricular thrombosis and cardioembolism.
  • Left ventricular ejection fraction (EF) has limitations in predicting these thrombotic events below certain thresholds.
  • Additional factors beyond EF contribute to variability in thrombosis risk.

Purpose of the Study:

  • To introduce and validate queue models for analyzing LV blood transit.
  • To connect flow component analysis with residence time (RT) mapping.
  • To elucidate the relationship between EF, direct flow (DF), residual volume (RV), and LV blood RT.

Main Methods:

  • Development of queue models providing closed-form expressions for average LV blood RT.
  • Validation of models against RT data from vector flow mapping in 332 subjects.
  • Inclusion of controls and patients with acute myocardial infarction (AMI), hypertrophic cardiomyopathy (HCM), and dilated cardiomyopathy (DCM).

Main Results:

  • LV blood RT becomes more sensitive to DF as EF decreases.
  • RT is minimized with first-in-first-out (FIFO) blood transit.
  • Direct flow (DF) disrupts FIFO patterns, prolonging RT and increasing blood stasis, especially at low EF.
  • FIFO models demonstrated good performance in assessing RT.

Conclusions:

  • Large direct flows (DF) exacerbate blood stasis in the LV when EF is low.
  • Queue models explain the limitations of EF as a sole predictor of intraventricular thrombosis risk.
  • These models offer a novel framework for understanding LV hemodynamics and thrombosis formation.

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