Shape Morphing and Slice Shift Correction in Congenital Heart Defect Model Generation

Conference Paper (2023)
Author(s)

Puck Pentenga (Student TU Delft)

Ashley Stroh (Dassault Systèmes Simulia Corporation)

Wouter van Genuchten (Erasmus MC)

Wim A. Helbing (Erasmus MC)

Mathias Peirlinck (TU Delft - Medical Instruments & Bio-Inspired Technology)

Research Group
Medical Instruments & Bio-Inspired Technology
Copyright
© 2023 Puck Pentenga, Ashley Stroh, Wouter van Genuchten, Wim A. Helbing, M. Peirlinck
DOI related publication
https://doi.org/10.1007/978-3-031-35302-4_36
More Info
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Publication Year
2023
Language
English
Copyright
© 2023 Puck Pentenga, Ashley Stroh, Wouter van Genuchten, Wim A. Helbing, M. Peirlinck
Research Group
Medical Instruments & Bio-Inspired Technology
Bibliographical Note
Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public. @en
Pages (from-to)
347-355
ISBN (print)
978-3-0313-5301-7
Reuse Rights

Other than for strictly personal use, it is not permitted to download, forward or distribute the text or part of it, without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license such as Creative Commons.

Abstract

Computational heart modeling is a promising approach for improving the prognosis of patients born with congenital heart defects. To create accurate physics-based digital cardiac twins of this population, it is crucial to accurately represent the highly diverse and unique subject-specific heart geometry. In young pediatric patients, this is a challenging endeavor given the lack of high-spatial-resolution imaging data and the risk of slice misalignment. In this study, we set up a multistep shape morphing and slice correction approach to accommodate these challenges and establish a population of biventricular heart models for a variety of healthy, Fallot, and Fontan pediatric patients.

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