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Parametrization of an in-silico circulatory simulation by clinical datasets – towards prediction of ventricular function following assist device implantation

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Published/Copyright: March 6, 2017

Abstract

Background:

Left ventricular assist device (LVAD) therapy has revolutionized the way end stage heart failure is treated today. Analysis of LVAD interaction with the whole cardiovascular system and its biological feedback loops is often conducted by means of computer models. Generating real time pressure volume loops (PV-loops) in patients, not using conductance catheters but routine diagnostics to feed an in-silico model could help to predict postoperative complications.

Methods:

Routinely obtained hemodynamic measurements to evaluate myocardial function prior to LVAD implantation like pressure readings in the aorta, the left atrium and the left ventricle and simultaneous three-dimensional (3D) echocardiography recordings were assessed to parametrize a reduced computational model of the cardiovascular system. An automatic parameter identification procedure has been developed.

Results:

The results constitute a patient-individual computational simulation model. An exemplary in-silico study focusing on the effect of different ventricular assist device (VAD) speeds has been conducted. Results allow for estimation of the resulting hemodynamic parameters and changes of the PV-loops.

Conclusion:

The model improves understanding and prediction of the interaction between pump and ventricles. Future modifications in exporting and merging routinely assessed real time hemodynamic patient data are necessary to investigate various clinical and pathological conditions of LVAD recipients.


Corresponding author: Andreas Goetzenich, MD, PhD, Department of Thoracic and Cardiovascular Surgery, University Hospital RWTH Aachen, Pauwelsstr. 30, 52074 Aachen, Germany, Phone: +49 241 80 35556, Fax: +49 241 80 333 555 6
aAjay Moza and Jonas Gesenhues: These authors contributed equally to this work.

Acknowledgments

This work was supported by the German Research Foundation (DFG) within the Smart Life Suport 2.0 PathoMod project (PAK 183-2). The authors declare to have no conflicting interests.

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Received: 2016-3-31
Accepted: 2017-1-12
Published Online: 2017-3-6
Published in Print: 2017-4-1

©2017 Walter de Gruyter GmbH, Berlin/Boston

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