Multi-class point cloud completion networks for 3D cardiac anatomy
reconstruction from cine magnetic resonance images
- URL: http://arxiv.org/abs/2307.08535v2
- Date: Tue, 18 Jul 2023 14:11:18 GMT
- Title: Multi-class point cloud completion networks for 3D cardiac anatomy
reconstruction from cine magnetic resonance images
- Authors: Marcel Beetz, Abhirup Banerjee, Julius Ossenberg-Engels, Vicente Grau
- Abstract summary: We propose a novel fully automatic surface reconstruction pipeline capable of reconstructing multi-class 3D cardiac anatomy meshes.
Its key component is a multi-class point cloud completion network (PCCN) capable of correcting both the sparsity and misalignment issues of the 3D reconstruction task.
- Score: 4.1448595037512925
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Cine magnetic resonance imaging (MRI) is the current gold standard for the
assessment of cardiac anatomy and function. However, it typically only acquires
a set of two-dimensional (2D) slices of the underlying three-dimensional (3D)
anatomy of the heart, thus limiting the understanding and analysis of both
healthy and pathological cardiac morphology and physiology. In this paper, we
propose a novel fully automatic surface reconstruction pipeline capable of
reconstructing multi-class 3D cardiac anatomy meshes from raw cine MRI
acquisitions. Its key component is a multi-class point cloud completion network
(PCCN) capable of correcting both the sparsity and misalignment issues of the
3D reconstruction task in a unified model. We first evaluate the PCCN on a
large synthetic dataset of biventricular anatomies and observe Chamfer
distances between reconstructed and gold standard anatomies below or similar to
the underlying image resolution for multiple levels of slice misalignment.
Furthermore, we find a reduction in reconstruction error compared to a
benchmark 3D U-Net by 32% and 24% in terms of Hausdorff distance and mean
surface distance, respectively. We then apply the PCCN as part of our automated
reconstruction pipeline to 1000 subjects from the UK Biobank study in a
cross-domain transfer setting and demonstrate its ability to reconstruct
accurate and topologically plausible biventricular heart meshes with clinical
metrics comparable to the previous literature. Finally, we investigate the
robustness of our proposed approach and observe its capacity to successfully
handle multiple common outlier conditions.
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