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CMRPredict TERMINATED

Patient specific magnetic resonance image guided biomechanical modelling of the heart – Anovel tool towards personalized medicine in heart failure

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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0

 CMRPredict project word cloud

Explore the words cloud of the CMRPredict project. It provides you a very rough idea of what is the project "CMRPredict" about.

considerable    prediction    accordingly    imaging    promise    cardiac    innovations    impose    cardiovascular    modalities    tensor    morphology    ultimately    50    disease    mechanics    patient    urgent    time    assessing    additional    standard    gold    diffusion    primarily    biomechanical    mortality    resonance       clinical    attracted    causes    structure    accuracy    scan    mass    models    compromises    magnetic    beating    first    population    ejection    routine    resolution    overcome    biophysical    diagnose    guide    predictive    local    heart    unfortunately    fellowship    sufficient    hf    preserved    sufficiently    spatial    patients    tools    guiding    world    limitations    insights    practical    significantly    progressing    once    myocardial    detected    individual    framework    guided    tool    vivo    made    data    microstructure    rate    microscopic    difficult    infarction    emerged    cmr    tissue    incorporating    treatment    progression    fraction    image    coverage    assumptions    diagnostic   

Project "CMRPredict" data sheet

The following table provides information about the project.

Coordinator
EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH 

Organization address
address: Raemistrasse 101
city: ZUERICH
postcode: 8092
website: https://www.ethz.ch/de.html

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Switzerland [CH]
 Total cost 247˙840 €
 EC max contribution 247˙840 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2016
 Funding Scheme MSCA-IF-GF
 Starting year 2017
 Duration (year-month-day) from 2017-09-01   to  2020-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH CH (ZUERICH) coordinator 247˙840.00
2    University of California San Francisco School of Medicine US (San Francisco) partner 0.00

Map

 Project objective

Heart failure (HF) is a progressing disease currently affecting 2% of the population in the developed world with a mortality rate of 50% within the first five years. While HF with reduced ejection fraction, primarily associated with myocardial infarction, can be detected with sufficient accuracy, HF with preserved ejection fraction is far more difficult to diagnose. Accordingly, there is an urgent need to better diagnose these patients to ultimately guide and improve treatment. Among the clinical imaging modalities, Cardiovascular Magnetic Resonance (CMR) is the gold standard for assessing cardiac mass and ejection fraction, and is capable to assess local cardiac mechanics and tissue properties. Beyond these established methods, cardiac diffusion tensor imaging has emerged as a new tool to enable insights into the microscopic morphology of the beating heart. Unfortunately, due to scan time limitations during clinical routine, compromises in spatial resolution and coverage have to be made. To overcome practical limitations of clinical in vivo CMR imaging and to enable prediction of disease progression for individual patients, additional tools are required. To this end, biomechanical models have attracted considerable attention. Once adapted sufficiently to in-vivo imaging, these models promise patient-specific insights into causes and progression of disease and, help guiding treatment. It is the objective of the present fellowship proposal to significantly advance patient-specific, image-guided modelling of HF by incorporating the most recent developments in both CMR imaging and biophysical modelling. The proposed framework will address limitations of current approaches, which impose generic assumptions about cardiac tissue properties and structure. With recent innovations in CMR imaging, as developed by the applicant, data on local changes of myocardial microstructure will be obtained to achieve the next level of diagnostic and predictive cardiac modelling of HF.

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The information about "CMRPREDICT" are provided by the European Opendata Portal: CORDIS opendata.

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