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Robust automated calcification meshing for personalized cardiovascular biomechanics.
Pak, Daniel H; Liu, Minliang; Kim, Theodore; Ozturk, Caglar; McKay, Raymond; Roche, Ellen T; Gleason, Rudolph; Duncan, James S.
Afiliación
  • Pak DH; Yale University, 300 Cedar St, New Haven, CT, 06511, USA. daniel.pak@yale.edu.
  • Liu M; Texas Tech University, 805 Boston Avenue, Lubbock, TX, 79409, USA.
  • Kim T; Yale University, 300 Cedar St, New Haven, CT, 06511, USA.
  • Ozturk C; Massachusetts Institute of Technology, 45 Carleton St, Cambridge, MA, 02142, USA.
  • McKay R; University of Southampton, University Road, Southampton, SO17 1BJ, UK.
  • Roche ET; Hartford Hospital, 85 Seymour St, Hartford, CT, 06106, USA.
  • Gleason R; Massachusetts Institute of Technology, 45 Carleton St, Cambridge, MA, 02142, USA.
  • Duncan JS; Georgia Institute of Technology, 315 Ferst Dr NW, Atlanta, GA, 30332, USA.
NPJ Digit Med ; 7(1): 213, 2024 Aug 15.
Article en En | MEDLINE | ID: mdl-39143242
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.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: NPJ Digit Med Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: NPJ Digit Med Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos