SeqSeg: Learning Local Segments for Automatic Vascular Model Construction
Numi Sveinsson Cepero, Shawn C. Shadden
TL;DR
SeqSeg presents a seed-initiated, sequential segmentation approach to automatic vascular model construction that operates on local subvolumes with a 3D U-Net. By iteratively tracing along vessel centerlines and handling bifurcations, SeqSeg builds a globally connected vascular segmentation and surface mesh, outperforming state-of-the-art global nnU-Net baselines in covering distal branches and maintaining topology. The method demonstrates robust generalization to unseen vascular regions and de novo data, with favorable Dice, Hausdorff, and centerline overlap metrics and improved connectivity for physics-based simulations. It leverages adaptive subvolume sizing, probabilistic fusion across overlaps, and explicit handling of vessels’ geometry to deliver simulation-ready vascular models more efficiently than global pixel-wise approaches. The work is supported by public datasets and open-source code, enabling reuse for broader vascular anatomies and future integration with multi-physics workflows.
Abstract
Computational modeling of cardiovascular function has become a critical part of diagnosing, treating and understanding cardiovascular disease. Most strategies involve constructing anatomically accurate computer models of cardiovascular structures, which is a multistep, time-consuming process. To improve the model generation process, we herein present SeqSeg (sequential segmentation): a novel deep learning based automatic tracing and segmentation algorithm for constructing image-based vascular models. SeqSeg leverages local U-Net-based inference to sequentially segment vascular structures from medical image volumes. We tested SeqSeg on CT and MR images of aortic and aortofemoral models and compared the predictions to those of benchmark 2D and 3D global nnU-Net models, which have previously shown excellent accuracy for medical image segmentation. We demonstrate that SeqSeg is able to segment more complete vasculature and is able to generalize to vascular structures not annotated in the training data.
