Evidence map›Paper›PMID 35737662›Full record

ArticlePloS one2022

Identifying locations susceptible to micro-anatomical reentry using a spatial network representation of atrial fibre maps.

Max Falkenberg, James A Coleman, Sam Dobson, David J Hickey, Louie Terrill, Alberto Ciacci, Belvin Thomas, Arunashis Sau, Fu Siong Ng, Jichao Zhao and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

12 authors at 2 institutions in 2 countries.

Max FalkenbergCentre for Complexity Science, Imperial College London, London, United Kingdom.ORCID 0000-0002-2986-2494
James A ColemanDepartment of Physics, Imperial College London, London, United Kingdom.
Sam DobsonDepartment of Physics, Imperial College London, London, United Kingdom.
David J HickeyDepartment of Physics, Imperial College London, London, United Kingdom.ORCID 0000-0003-0149-712X
Louie TerrillDepartment of Physics, Imperial College London, London, United Kingdom.ORCID 0000-0002-0237-794X
Alberto CiacciCentre for Complexity Science, Imperial College London, London, United Kingdom.
Belvin ThomasAuckland Bioengineering Institute, The University of Auckland, Auckland, New Zealand.ORCID 0000-0001-6012-7212
Arunashis SauElectroCardioMaths Programme, Imperial Centre for Cardiac Engineering, National Heart & Lung Institute, Imperial College London, London, United Kingdom.ORCID 0000-0002-0204-7078
Fu Siong NgElectroCardioMaths Programme, Imperial Centre for Cardiac Engineering, National Heart & Lung Institute, Imperial College London, London, United Kingdom.
Jichao ZhaoAuckland Bioengineering Institute, The University of Auckland, Auckland, New Zealand.
Nicholas S PetersElectroCardioMaths Programme, Imperial Centre for Cardiac Engineering, National Heart & Lung Institute, Imperial College London, London, United Kingdom.
Kim ChristensenCentre for Complexity Science, Imperial College London, London, United Kingdom.
Imperial College London · GBUniversity of Auckland · NZ

Funding

British Heart Foundation FS/CRTF/21/24183British Heart Foundation RG/16/3/32175British Heart Foundation RG/F/22/110078
6 · The paper itself

Abstract

Micro-anatomical reentry has been identified as a potential driver of atrial fibrillation (AF). In this paper, we introduce a novel computational method which aims to identify which atrial regions are most susceptible to micro-reentry. The approach, which considers the structural basis for micro-reentry only, is based on the premise that the accumulation of electrically insulating interstitial fibrosis can be modelled by simulating percolation-like phenomena on spatial networks. Our results suggest that at high coupling, where micro-reentry is rare, the micro-reentrant substrate is highly clustered in areas where the atrial walls are thin and have convex wall morphology, likely facilitating localised treatment via ablation. However, as transverse connections between fibres are removed, mimicking the accumulation of interstitial fibrosis, the substrate becomes less spatially clustered, and the bias to forming in thin, convex regions of the atria is reduced, possibly restricting the efficacy of localised ablation. Comparing our algorithm on image-based models with and without atrial fibre structure, we find that strong longitudinal fibre coupling can suppress the micro-reentrant substrate, whereas regions with disordered fibre orientations have an enhanced risk of micro-reentry. With further development, these methods may be useful for modelling the temporal development of the fibrotic substrate on an individualised basis.

Indexed as

Atrial FibrillationCatheter AblationFibrosisHeart AtriaHumans

Identifiers

PMID35737662
PMCPMC9223322
OpenAlexW4283331810

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.