Evidence map›Paper›PMID 30420809›Full record

ArticleFrontiers in physiology2018

Muscle Thickness and Curvature Influence Atrial Conduction Velocities.

Simone Rossi, Stephen Gaeta, Boyce E Griffith, Craig S Henriquez

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Automated analysis of electrogram characteristics in baseline rhythm can distinguish isthmus regions and segments in reentrant ventricular tachycardia.Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing · 2026
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  8. Identification of local atrial conduction heterogeneities using high-density conduction velocity estimation.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2021
    Article
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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

4 authors at 3 institutions in 1 country.

Simone RossiCardiovascular Modeling and Simulation Laboratory, Carolina Center for Interdisciplinary Applied Mathematics, University of North Carolina, Chapel Hill, NC, United States.
Stephen GaetaClinical Cardiac Electrophysiology/Cardiology Division, Duke University Medical Center, Durham, NC, United States.
Boyce E GriffithCardiovascular Modeling and Simulation Laboratory, Carolina Center for Interdisciplinary Applied Mathematics, University of North Carolina, Chapel Hill, NC, United States.
Craig S HenriquezDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC, United States.
Applied Physical Sciences (United States) · USDuke Medical Center · USDuke University · US

Funding

Multiscale Modeling of Clotting Risk in Atrial FibrillationU01HL143336 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GRIFFITH, BOYCE EUGENE · 2018 to 2022
$2.8M
Mathematical modeling and computer simulation of aortic dissectionR01HL117063 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GRIFFITH, BOYCE EUGENE · 2013 to 2017
$2.3M
NHLBI NIH HHS R01 HL117063NHLBI NIH HHS U01 HL143336
6 · The paper itself

Abstract

Electroanatomical mapping is currently used to provide clinicians with information about the electrophysiological state of the heart and to guide interventions like ablation. These maps can be used to identify ectopic triggers of an arrhythmia such as atrial fibrillation (AF) or changes in the conduction velocity (CV) that have been associated with poor cell to cell coupling or fibrosis. Unfortunately, many factors are known to affect CV, including membrane excitability, pacing rate, wavefront curvature, and bath loading, making interpretation challenging. In this work, we show how endocardial conduction velocities are also affected by the geometrical factors of muscle thickness and wall curvature. Using an idealized three-dimensional strand, we show that transverse conductivities and boundary conditions can slow down or speed up signal propagation, depending on the curvature of the muscle tissue. In fact, a planar wavefront that is parallel to a straight line normal to the mid-surface does not remain normal to the mid-surface in a curved domain. We further demonstrate that the conclusions drawn from the idealized test case can be used to explain spatial changes in conduction velocities in a patient-specific reconstruction of the left atrial posterior wall. The simulations suggest that the widespread assumption of treating atrial muscle as a two-dimensional manifold for electrophysiological simulations will not accurately represent the endocardial conduction velocities in regions of the heart thicker than 0.5 mm with significant wall curvature.

Indexed as

atrial fibrillationbath-loading conditionsbidomain modelcardiac electrophysiologyconduction velocityelectroanatomical mappingleft atrial posterior wall

Identifiers

PMID30420809
PMCPMC6215968
OpenAlexW2898915656

What OpenQuestion holds

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LicenceCC BY
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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.