mlsanityData to 7 Oct 2026

Automated generation of 0D and 1D reduced-order models of patient-specific blood flow

arXiv 2111.04878 ↗First posted 8 Nov 2021cs.CEcited by 15

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Abstract (arXiv)

Three-dimensional (3D) cardiovascular fluid dynamics simulations typically require hours to days of computing time on a high-performance computing cluster. One-dimensional (1D) and lumped-parameter zero-dimensional (0D) models show great promise for accurately predicting blood bulk flow and pressure waveforms with only a fraction of the cost. They can also accelerate uncertainty quantification, optimization, and design parameterization studies. Despite several prior studies generating 1D and 0D models and comparing them to 3D solutions, these were typically limited to either 1D or 0D and a singular category of vascular anatomies. This work proposes a fully automated and openly available framework to generate and simulate 1D and 0D models from 3D patient-specific geometries, automatically detecting vessel junctions and stenosis segments. Our only input is the 3D geometry; we do not use any prior knowledge from 3D simulations. All computational tools presented in this work are implemented in the open-source software platform SimVascular. We demonstrate the reduced-order approximation quality against rigid-wall 3D solutions in a comprehensive comparison with N=72 publicly available models from various anatomies, vessel types, and disease conditions. Relative average approximation errors of flows and pressures typically ranged from 1% to 10% for both 1D and 0D models, measured at the outlets of terminal vessel branches. In general, 0D model errors were only slightly higher than 1D model errors despite requiring only a third of the 1D runtime. Automatically generated ROMs can significantly speed up model development and shift the computational load from high-performance machines to personal computers.

Key facts. Cited by 15 papers in the map (data through 7 Oct 2026). First posted on arXiv 8 Nov 2021.

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Cited by year (2026 to 7 Oct)

Citing papers per year: 2022: 1; 2023: 2; 2024: 3; 2025: 4; 2026: 5.

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  1. 2023Learning Reduced-Order Models for Cardiovascular Simulations with Graph Neural Networkscited by 20
  2. 2023A Probabilistic Neural Twin for Treatment Planning in Peripheral Pulmonary Artery Stenosiscited by 3
  3. 2024Quantification of total uncertainty in the physics-informed reconstruction of CVSim-6 physiologycited by 3
  4. 2025Learning Hemodynamic Scalar Fields on Coronary Artery Meshes: A Benchmark of Geometric Deep Learning Modelscited by 2
  5. 2022Deep learning-based surrogate model for 3-D patient-specific computational fluid dynamicscited by 1
  6. 2024InVAErt networks for amortized inference and identifiability analysis of lumped parameter hemodynamic modelscited by 1
  7. 2024Data-driven discovery of mechanical models directly from MRI spectral datacited by 1
  8. 2025GReAT: leveraging geometric artery data to improve wall shear stress assessmentcited by 1
  9. 2025Data-Driven Bifurcation Handling in Physics-Based Reduced-Order Vascular Hemodynamic Modelscited by 1
  10. 2025On the performance of multi-fidelity and reduced-dimensional neural emulators for inference of physiological boundary conditionscited by 0
  11. 2026FalconBC: Flow matching for Amortized inference of Latent-CONditioned physiologic Boundary Conditionscited by 0
  12. 2026Real-Time Surrogate Modeling for Personalized Blood Flow Prediction and Hemodynamic Analysiscited by 0
3 more
  1. 2026Asymptotic-Preserving Neural Networks for Viscoelastic Parameter Identification in Multiscale Blood Flow Modelingcited by 0
  2. 2026Tokenised Flow Matching for Hierarchical Simulation Based Inferencecited by 0
  3. 2026Same Branches, Different Trees: A Bifurcation Connectedness Metric for Coronary Artery Segmentation and FFR-CT Decision Agreementcited by 0