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PMID: 25157924 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Towards a fast and efficient approach for modelling the patient-specific ventricular haemodynamics.

Progress in biophysics and molecular biology ·Vol. 116 ·No. 1 ·2014-09-00 ·页码 3-10

de Vecchi A, Gomez A, Pushparajah K, Schaeffter T, Nordsletten DA, Simpson JM, Penney GP, Smith NP

Abstract

Computer modelling of the heart has emerged over the past decade as a powerful technique to explore the cardiovascular pathophysiology and inform clinical diagnosis. The current state-of-the-art in biophysical modelling requires a wealth of, potentially invasive, clinical data for the parametrisation and validation of the models, a process that is still too long and complex to be compatible with the clinical decision-making time. Therefore, there remains a need for models that can be quickly customised to reconstruct physical processes difficult to measure directly in patients. In this paper, we propose a less resource-intensive approach to modelling, whereby computational fluid-dynamics (CFD) models are constrained exclusively by boundary motion derived from imaging data through a validated wall tracking algorithm. These models are generated and parametrised based solely on ultrasound data, whose acquisition is fast, inexpensive and routine in all patients. To maximise the time and computational efficiency, a semi-automated pipeline is embedded in an image processing workflow to personalise the models. Applying this approach to two patient cases, we demonstrate this tool can be directly used in the clinic to interpret and complement the available clinical data by providing a quantitative indication of clinical markers that cannot be easily derived from imaging, such as pressure gradients and the flow energy.

Keywords
3D blood flow reconstruction B-Mode echocardiography Cardiac haemodynamics Colour Doppler Personalized numerical modelling
MeSH 主题词
Blood Flow Velocity/physiology Blood Pressure/physiology Computer Simulation Humans Imaging, Three-Dimensional/methods Models, Cardiovascular Myocardial Contraction/physiology Patient-Specific Modeling Rheology/methods Ventricular Function/physiology
作者与单位
共 8 位作者,点击展开单位 / ORCID
de Vecchi A
Division of Imaging Sciences and Biomedical Engineering, King's College London, St. Thomas' Hospital, London SE1 7EH, UK.
Gomez A
Division of Imaging Sciences and Biomedical Engineering, King's College London, St. Thomas' Hospital, London SE1 7EH, UK.
Pushparajah K
Evelina London Children's Hospital, London SE1 7EH, UK.
Schaeffter T
Division of Imaging Sciences and Biomedical Engineering, King's College London, St. Thomas' Hospital, London SE1 7EH, UK.
Nordsletten D A
Division of Imaging Sciences and Biomedical Engineering, King's College London, St. Thomas' Hospital, London SE1 7EH, UK.
Simpson J M
Evelina London Children's Hospital, London SE1 7EH, UK.
Penney G P
Division of Imaging Sciences and Biomedical Engineering, King's College London, St. Thomas' Hospital, London SE1 7EH, UK.
Smith N P
Division of Imaging Sciences and Biomedical Engineering, King's College London, St. Thomas' Hospital, London SE1 7EH, UK. Electronic address: [email protected].
Article Info
Journal
Progress in biophysics and molecular biology
Abbr.
Prog Biophys Mol Biol
ISSN
1873-1732
Corresponding email
Published
2014-09-00
电子出版
2014-00-23
页码
3-10
Language
English
Country/Region
England
NLM ID
0401233
基金资助
British Heart Foundation · NH/11/5/29058 · United Kingdom
Wellcome Trust · WT088641/Z/09/Z · United Kingdom
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