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Lea J. Köglmeier

Publications and source records attributed to Lea J. Köglmeier.

2 recordsLinked to original sources

Multi-Physics-Enhanced Bayesian Inverse Analysis: Information Gain from Additional Fields

Inverse analysis, such as model calibration, often suffers from a lack of informative data in complex real-world scenarios. The standard remedy, designing new experimental setups, is often costly and time-consuming, while readily available but seemingly useless data are ignored. This work proposes incorporating such data from additional physical fields into the inverse analysis, even when the forward model solves a single-physics problem. A Bayesian framework easily incorporates the additional data and quantifies the resulting uncertainty reduction. We formally introduce the proposed method, which we denote as multi-physics-enhanced Bayesian inverse analysis. Moreover, this work is the first to quantify the reduction in parameter uncertainty by comparing the information gain from the prior to the posterior when using single-physics versus multi-physics data. We demonstrate the potential of the proposed method in two exemplary applications. Our results show that even a few or noisy data points from an additional physical field can considerably increase the information gain, even when the physical field is only weakly or one-way coupled. Overall, this work proposes and promotes the future use of multi-physics-enhanced Bayesian inverse analysis as a cost- and time-saving game-changer across various fields of science and industry, particularly in medicine.

cs.CE↗

Pressure- and time-dependent alveolar recruitment/derecruitment in a spatially resolved patient-specific computational model for injured human lungs

We present a novel computational model for the dynamics of alveolar recruitment/derecruitment (RD), which reproduces the underlying characteristics typically observed in injured lungs. The basic idea is a pressure- and time-dependent variation of the stress-free reference volume in reduced dimensional viscoelastic elements representing the acinar tissue. We choose a variable reference volume triggered by critical opening and closing pressures in a time-dependent manner from a straightforward mechanical point of view. In the case of (partially and progressively) collapsing alveolar structures, the volume available for expansion during breathing reduces and vice versa, eventually enabling consideration of alveolar collapse and reopening in our model. We further introduce a method for patient-specific determination of the underlying critical parameters of the new alveolar RD dynamics when integrated into the tissue elements, referred to as terminal units, of a spatially resolved physics-based lung model that simulates the human respiratory system in an anatomically correct manner. Relevant patient-specific parameters of the terminal units are herein determined based on medical image data and the macromechanical behavior of the lung during artificial ventilation. We test the whole modeling approach for a real-life scenario by applying it to the clinical data of a mechanically ventilated patient. The generated lung model is capable of reproducing clinical measurements such as tidal volume and pleural pressure during various ventilation maneuvers. We conclude that this new model is an important step toward personalized treatment of ARDS patients by considering potentially harmful mechanisms - such as cyclic RD and overdistension - and might help in the development of relevant protective ventilation strategies to reduce ventilator-induced lung injury (VILI).

physics.med-ph↗