Robust automated calcification meshing for personalized cardiovascular biomechanics

Calcification has significant influence over cardiovascular diseases and interventions. Detailed characterization of calcification is thus desired for predictive modeling, but calcium deposits on cardiovascular structures are still often manually reconstructed for physics-driven simulations. This poses a major bottleneck for large-scale adoption of computational simulations for research or clinical use. To address this, we propose an end-to-end automated image-to-mesh algorithm that enables robust incorporation of patient-specific calcification onto a given cardiovascular tissue mesh. The algorithm provides a substantial speed-up from several hours of manual meshing to ~1 min of automated computation, and it solves an important problem that cannot be addressed with recent template-based meshing techniques. We validated our final calcified tissue meshes with extensive simulations, demonstrating our ability to accurately model patient-specific aortic stenosis and Transcatheter Aortic Valve Replacement. Our method may serve as an important tool for accelerating the development and usage of personalized cardiovascular biomechanics.

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Publication Details

Journal
npj Digital Medicine
Published
2024-08-15
DOI
https://doi.org/10.1038/s41746-024-01202-9
Citations
2
Primary Topic
Cardiac Valve Diseases and Treatments
Type
article
Field-Weighted Citation Impact
0.80

Funders

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article

Robust automated calcification meshing for personalized cardiovascular biomechanics

Çağlar Öztürk, Ellen T. Roche, James S. Duncan, Rudolph L. Gleason et al.
2 citations
npj Digital Medicine
Cardiac Valve Diseases and Treatments
0.80
article

Robust automated calcification meshing for personalized cardiovascular biomechanics

Çağlar Öztürk, Ellen T. Roche, James S. Duncan, Rudolph L. Gleason, Daniel H. Pak, Minliang Liu, Raymond G. McKay, Theodore Kim
article en
2 citations

Abstract

Calcification has significant influence over cardiovascular diseases and interventions. Detailed characterization of calcification is thus desired for predictive modeling, but calcium deposits on cardiovascular structures are still often manually reconstructed for physics-driven simulations. This poses a major bottleneck for large-scale adoption of computational simulations for research or clinical use. To address this, we propose an end-to-end automated image-to-mesh algorithm that enables robust incorporation of patient-specific calcification onto a given cardiovascular tissue mesh. The algorithm provides a substantial speed-up from several hours of manual meshing to ~1 min of automated computation, and it solves an important problem that cannot be addressed with recent template-based meshing techniques. We validated our final calcified tissue meshes with extensive simulations, demonstrating our ability to accurately model patient-specific aortic stenosis and Transcatheter Aortic Valve Replacement. Our method may serve as an important tool for accelerating the development and usage of personalized cardiovascular biomechanics.

npj Digital MedicineVol. 7(1)
Texas Tech University (US), Hartford Hospital (US), Georgia Institute of Technology (US), Yale University (US), University of Southampton (GB), Massachusetts Institute of Technology (US)
Texas Tech University, National Institutes of Health, National Heart, Lung, and Blood Institute
Zero hunger
Openalex Percentile: Top 24%
Cardiac Valve Diseases and Treatments
0.80
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