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@PHDTHESIS{Haler:1025082,
      author       = {Haßler, Stefan Thomas},
      othercontributors = {Behr, Marek and Steinseifer, Ulrich},
      title        = {{M}odeling and simulation of blood damage in medical
                      devices},
      school       = {Rheinisch-Westfälische Technische Hochschule Aachen},
      type         = {Dissertation},
      address      = {Aachen},
      publisher    = {RWTH Aachen University},
      reportid     = {RWTH-2026-00517},
      pages        = {1 Online-Ressource : Illustrationen},
      year         = {2025},
      note         = {Veröffentlicht auf dem Publikationsserver der RWTH Aachen
                      University 2026; Dissertation, Rheinisch-Westfälische
                      Technische Hochschule Aachen, 2025},
      abstract     = {Heart failure is the main cause of death in developed
                      countries. A heart transplantation is not available for most
                      patients, due to the shortage of donor organs. Ventricular
                      assist devices (VADs) that support the failing heart for
                      several years, can be used as a bridge to transplant or even
                      as a bridge to recovery. However, their development is
                      complicated, costly and time-consuming, while the
                      availability of blood samples for in-vitro tests is limited
                      at the same time. The reliable computational prediction of
                      blood flow and blood damage within a VAD is a very valuable
                      tool in the design phase. While the flow prediction with
                      computational fluid dynamics is well established in
                      engineering, the prediction of blood damage using
                      computational hemodynamics is a matter of ongoing
                      research.This thesis provides a numerically stable approach
                      to hemolysis prediction for complex domains, that tries to
                      take the physiological behavior of red blood cells (RBCs)
                      into account. Here, we follow a three-step-approach: the
                      blood flow is computed first; then we predict the
                      deformation of RBCs within that flow field, using the
                      so-called morphology model; the release of hemoglobin to the
                      blood plasma is finally predicted by a pore formation model,
                      based on the RBCs deformation and the flow properties.
                      Especially the morphology simulation is very challenging,
                      due to the frequent occurrence of unphysical, negative
                      eigenvalues in the shape tensor, which lead to diverging
                      simulations. We apply a logarithmic transformation of the
                      shape tensor — inspired by the work of Knechtges — that
                      preserve the positive eigenvalues by design, and derive its
                      variational multiscale (VMS) stabilized finite element
                      formulation. The usage of the pore formation model — first
                      proposed by Vitale et al. — in an Eulerian frame of
                      reference, is a novelty of this thesis. Furthermore, we
                      propose to consistently use the multiple reference frames
                      (MRF) approach for all three simulation steps, for which we
                      derive the constitutive equations. This allows faster,
                      steady-state simulations, which result in time-averaged
                      approximations to the, in principle, transient fields. It
                      lets us compute the quantities-of-interest directly, like
                      the pressure head provided by the pump or the averaged
                      plasma-free hemoglobin content at the outflow, which are
                      also obtained by experiments.Our model predictions show a
                      good agreement with experimental results for the FDA’s
                      benchmark blood pump. Furthermore, we use this modeling
                      approach to predict the hemocompatibility of a
                      state-of-the-art centrifugal VAD.},
      cin          = {416010},
      ddc          = {620},
      cid          = {$I:(DE-82)416010_20140620$},
      typ          = {PUB:(DE-HGF)11},
      doi          = {10.18154/RWTH-2026-00517},
      url          = {https://publications.rwth-aachen.de/record/1025082},
}