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Updated: Sep 20, 2025

Human Fetal Blood Flow Quantification with Magnetic Resonance Imaging and Motion Compensation
Published on: January 7, 2021
A Novel Prenatal Pipeline for Three-Dimensional Hemodynamic Modeling of the Fetal Aorta
Joanne Sarsam1, Angela Desmond2,3, Mehrdad Roustaei4
1Department of Computational and Systems Biology, UCLA, Los Angeles, California, USA.
Insights
This study introduces a new method to create 3D models of the fetal aorta from 2D echocardiograms, enabling noninvasive hemodynamic predictions for congenital heart disease (CHD) diagnosis.
Area of Science:
- Biomedical Engineering
- Cardiovascular Research
- Medical Imaging
Background:
- Congenital heart disease (CHD) is a leading cause of infant mortality.
- Standard fetal echocardiography lacks detailed hemodynamic insights.
- Existing computational models rely on 3D imaging, not readily available for fetal diagnosis.
Purpose of the Study:
- To develop a methodology for creating pulsatile 3D aortic models from 2D fetal echocardiograms.
- To enable noninvasive prediction of fetal hemodynamics for improved CHD diagnosis.
- To bridge the gap between standard imaging and advanced computational modeling in prenatal care.
Main Methods:
- Utilized 2D fetal echocardiograms with edge detection algorithms for vessel segmentation.
- Reconstructed 3D geometric models of the aortic arch using SimVascular.
- Developed patient-specific simulations for fetuses with and without coarctation of the aorta (CoA).
Main Results:
- Proposed a validated methodology for physiologically reasonable fetal hemodynamic quantification.
- Generated noninvasive predictions of fetal aortic pressures and flow patterns.
- Demonstrated insight into the impact of abnormal morphology on prenatal aortic flow.
Conclusions:
- Presented a clinically applicable pipeline for fetal aortic flow simulations.
- Captured fluid-structure interactions and predicted diagnostic hemodynamic indicators noninvasively.
- Enhanced diagnostic precision for CHD by integrating patient-specific physiology beyond morphology visualization.
Objective:
Congenital heart disease (CHD) is the most common birth defect and the leading cause of infant death from congenital anomalies. Limitations in standard-of-care fetal echocardiography lack hemodynamic insight. Cardiovascular computational modeling methods have been developed to simulate patient-specific morphology and hemodynamics, but are limited in applications for fetal diagnosis, as existing pipelines depend upon 3D CMR imaging data. There is no existing workflow for converting 2D echocardiograms into models of the fetal aorta. We aim to develop a methodology to create pulsatile 3D-aortic models from standard-of-care 2D echocardiograms to supplement fetal imaging with noninvasive predictions of hemodynamics in CHD diagnosis.
Methods:
Utilizing 2D fetal echocardiograms, edge detection algorithms are applied to delineate vessel boundaries. Cross-sectional diameters along the aortic arch and branch centerlines were segmented, integrated into 3D geometric models, and reconstructed using SimVascular. Patient-specific simulations were developed for three false-positive coarctation of the aorta (CoA) fetuses and 3 true positive CoA fetuses (postnatally confirmed), using echocardiogram and Doppler source data.
Results:
We propose a modeling methodology and set of boundary conditions that generate physiologically reasonable and cross-validated quantifications of fetal hemodynamics. Noninvasive predictions of fetal aortic pressures, flow streamlines, and vessel displacement offer insight into real-time hemodynamics and the stress of abnormal morphology on flow directions in the prenatal aorta.
Conclusions:
We present a clinically useful pipeline for generating simulations of flow in the fetal aorta that capture fluid-structure interactions and generate noninvasive predictions of diagnostic hemodynamic indicators that could not previously be captured prenatally. This pipeline integrates into clinical diagnosis and offers insight into patient-specific physiology beyond a visualization of cardiac morphology alone, offering the potential to enhance the diagnostic precision of CHDs.
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