Evidence map›Paper›PMID 23113842›Full record

ArticleComputer methods in biomechanics and biomedical engineering2014

Computational modelling of electrocardiograms: repolarisation and T-wave polarity in the human heart.

Daniel E Hurtado, Ellen Kuhl

Abstract read
In one paragraph

Article in Computer methods in biomechanics and biomedical engineering, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 37 citations in OpenAlex.

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  9. Predicting the cardiac toxicity of drugs using a novel multiscale exposure-response simulator.Computer methods in biomechanics and biomedical engineering · 2018
    Article
  10. Article
  11. The importance of mechano-electrical feedback and inertia in cardiac electromechanics.Computer methods in applied mechanics and engineering · 2017
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  16. Computational modeling of chemo-electro-mechanical coupling: a novel implicit monolithic finite element approach.International journal for numerical methods in biomedical engineering · 2013
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Daniel E Hurtadoa Department of Structural and Geotechnical Engineering, Biomedical Engineering Group , Pontificia Universidad Católica de Chile , Santiago , Chile.
Ellen Kuhl
Pontificia Universidad Católica de Chile · CLStanford University · US

Funding

Physics-based Simulation of Biological Structures(RMI)U54GM072970 · NIGMS · STANFORD UNIVERSITY · PI ALTMAN, RUSS BIAGIO · 2004 to 2013
$33.5M
NIGMS NIH HHS U54 GM072970
6 · The paper itself

Abstract

For more than a century, electrophysiologists, cardiologists and engineers have studied the electrical activity of the human heart to better understand rhythm disorders and possible treatment options. Although the depolarisation sequence of the heart is relatively well characterised, the repolarisation sequence remains a subject of great controversy. Here, we study regional and temporal variations in both depolarisation and repolarisation using a finite element approach. We discretise the governing equations in time using an unconditionally stable implicit Euler backward scheme and in space using a consistently linearised Newton-Raphson-based finite element solver. Through systematic parameter-sensitivity studies, we establish a direct relation between a normal positive T-wave and the non-uniform distribution of the controlling parameter, which we have termed refractoriness. To establish a healthy baseline model, we calibrate the refractoriness using clinically measured action potential durations at different locations in the human heart. We demonstrate the potential of our model by comparing the computationally predicted and clinically measured depolarisation and repolarisation profiles across the left ventricle. The proposed framework allows us to explore how local action potential durations on the microscopic scale translate into global repolarisation sequences on the macroscopic scale. We anticipate that our calibrated human heart model can be widely used to explore cardiac excitation in health and disease. For example, our model can serve to identify optimal pacing sites in patients with heart failure and to localise optimal ablation sites in patients with cardiac fibrillation.

Indexed as

Computer SimulationElectrocardiographyModels, CardiovascularAction PotentialsFinite Element AnalysisHeartHumans

Identifiers

PMID23113842
PMCPMC3574176
OpenAlexW2106301723

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.