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      Model-Based Therapy Planning Allows Prediction of Haemodynamic Outcome after Aortic Valve Replacement

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          Abstract

          Optimizing treatment planning is essential for advances in patient care and outcomes. Precisely tailored therapy for each patient remains a yearned-for goal. Cardiovascular modelling has the potential to simulate and predict the functional response before the actual intervention is performed. The objective of this study was to proof the validity of model-based prediction of haemodynamic outcome after aortic valve replacement. In a prospective study design virtual (model-based) treatment of the valve and the surrounding vasculature were performed alongside the actual surgical procedure (control group). The resulting predictions of anatomic and haemodynamic outcome based on information from magnetic resonance imaging before the procedure were compared to post-operative imaging assessment of the surgical control group in ten patients. Predicted vs. post-operative peak velocities across the valve were comparable (2.97 ± 1.12 vs. 2.68 ± 0.67 m/s; p = 0.362). In wall shear stress (17.3 ± 12.3 Pa vs. 16.7 ± 16.84 Pa; p = 0.803) and secondary flow degree (0.44 ± 0.32 vs. 0.49 ± 0.23; p = 0.277) significant linear correlations (p < 0.001) were found between predicted and post-operative outcomes. Between groups blood flow patterns showed good agreement (helicity p = 0.852, vorticity p = 0.185, eccentricity p = 0.333). Model-based therapy planning is able to accurately predict post-operative haemodynamics after aortic valve replacement. These validated virtual treatment procedures open up promising opportunities for individually targeted interventions.

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          The path to personalized medicine.

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            Aortic dilatation in patients with bicuspid aortic valve.

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              Bicuspid aortic cusp fusion morphology alters aortic three-dimensional outflow patterns, wall shear stress, and expression of aortopathy.

              Aortic 3-dimensional blood flow was analyzed to investigate altered ascending aorta (AAo) hemodynamics in bicuspid aortic valve (BAV) patients and its association with differences in cusp fusion patterns (right-left, RL versus right-noncoronary, RN) and expression of aortopathy. Four-dimensional flow MRI measured in vivo 3-dimensional blood flow in the aorta of 75 subjects: BAV patients with aortic dilatation stratified by leaflet fusion pattern (n=15 RL-BAV, mid AAo diameter=39.9±4.4 mm; n=15 RN-BAV, 39.6±7.2 mm); aorta size controls with tricuspid aortic valves (n=30, 41.0±4.4 mm); healthy volunteers (n=15, 24.9±3.0 mm). Aortopathy type (0-3), systolic flow angle, flow displacement, and regional wall shear stress were determined for all subjects. Eccentric outflow jet patterns in BAV patients resulted in elevated regional wall shear stress (P<0.0125) at the right-anterior walls for RL-BAV and right-posterior walls for RN-BAV in comparison with aorta size controls. Dilatation of the aortic root only (type 1) or involving the entire AAo and arch (type 3) was found in the majority of RN-BAV patients (87%) but was mostly absent for RL-BAV patients (87% type 2). Differences in aortopathy type between RL-BAV and RN-BAV patients were associated with altered flow displacement in the proximal and mid AAo for type 1 (42%-81% decrease versus type 2) and distal AAo for type 3 (33%-39% increase versus type 2). The presence and type of BAV fusion was associated with changes in regional wall shear stress distribution, systolic flow eccentricity, and expression of BAV aortopathy. Hemodynamic markers suggest a physiological mechanism by which the valve morphology phenotype can influence phenotypes of BAV aortopathy.
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                Author and article information

                Contributors
                mkelm@dhzb.de
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                29 August 2017
                29 August 2017
                2017
                : 7
                : 9897
                Affiliations
                [1 ]German Heart Centre Berlin, Department of Congenital Heart Disease, Unit of Cardiovascular Imaging, Berlin, Germany
                [2 ]ISNI 0000 0001 2218 4662, GRID grid.6363.0, , Charité – Universitätsmedizin Berlin, Biofluid Mechanics Laboratory, ; Berlin, Germany
                [3 ]ISNI 0000 0001 2218 4662, GRID grid.6363.0, , Charité – Universitätsmedizin Berlin, Department of Paediatric Cardiology, ; Berlin, Germany
                [4 ]German Heart Centre Berlin, Department of Cardiothoracic and Vascular Surgery, Berlin, Germany
                [5 ]DZHK (German Centre for Cardiovascular Research), Partner Site Berlin, Berlin, Germany
                [6 ]ISNI 0000 0001 2218 4662, GRID grid.6363.0, , Charité - Universitätsmedizin Berlin, Department of Cardiothoracic and Vascular Surgery, ; Berlin, Germany
                [7 ]ISNI 0000 0001 2218 4662, GRID grid.6363.0, Institute for Computational and Imaging Science in Cardiovascular Medicine, , Charité – Universitätsmedizin Berlin, ; Berlin, Germany
                [8 ]Lynkeus Srl, Rome, Italy
                [9 ]ISNI 0000000121901201, GRID grid.83440.3b, Institute for Cardiovascular Science, , University College London, ; London, UK
                [10 ]ISNI 0000 0001 0727 6809, GRID grid.414125.7, Department of Cardiology, , Ospedale Pediatrico Bambino Gesù, ; Rome, Italy
                [11 ]ISNI 0000 0000 9261 3939, GRID grid.4561.6, Cardiovascular Research & Development, , Fraunhofer-Gesellschaft zur Förderung der Angewandten Forschung E.V., ; Bremen, Germany
                [12 ]Image Analytics, Siemens Healthineers, Erlangen, Germany
                [13 ]ISNI 0000 0000 9219 5570, GRID grid.421171.0, , ESI Group, ; Paris, France
                [14 ]ISNI 0000 0000 8988 2476, GRID grid.11598.34, Department of Biophysics, , Medizinische Universität Graz, ; Graz, Austria
                [15 ]GRID grid.436251.7, , Maat France Sarl, ; Argonay, France
                [16 ]ISNI 0000 0001 0789 5319, GRID grid.13063.37, , LSE Health, London School of Economics and Political Science, ; London, UK
                Article
                3693
                10.1038/s41598-017-03693-x
                5575088
                28851875
                cf51033a-d262-437b-9f14-9b101aa67346
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 15 December 2016
                : 26 April 2017
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