Evidence map›Paper›PMID 31542646›Full record

ArticleComputers in biology and medicine2019

A robust computational framework for estimating 3D Bi-Atrial chamber wall thickness.

Yufeng Wang, Zhaohan Xiong, Aaqel Nalar, Brian J Hansen, Sanjay Kharche, Gunnar Seemann, Axel Loewe, Vadim V Fedorov, Jichao Zhao

Abstract read
In one paragraph

Article in Computers in biology and medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

9 authors.

Yufeng WangAuckland Bioengineering Institute, The University of Auckland, Auckland, 1142, New Zealand.
Zhaohan XiongAuckland Bioengineering Institute, The University of Auckland, Auckland, 1142, New Zealand.
Aaqel NalarAuckland Bioengineering Institute, The University of Auckland, Auckland, 1142, New Zealand.
Brian J HansenDepartment of Physiology and Cell Biology, The Ohio State University Wexner Medical Center, Columbus, USA.
Sanjay KharcheDepartment of Medical Biophysics, Western University, Canada.
Gunnar SeemannThe Institute for Experimental Cardiovascular Medicine, University Heart Center Freiburg, Bad Krozingen, Faculty of Medicine, Albert-Ludwigs University, Freiburg, Germany.
Axel LoeweThe Institute of Biomedical Engineering, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Vadim V FedorovDepartment of Physiology and Cell Biology, The Ohio State University Wexner Medical Center, Columbus, USA.
Jichao ZhaoAuckland Bioengineering Institute, The University of Auckland, Auckland, 1142, New Zealand. Electronic address: j.zhao@auckland.ac.nz.

Funding

Targeting the Arrhythmogenic Sources of Human Atrial FibrillationR01HL135109 · NHLBI · OHIO STATE UNIVERSITY · PI Vadim V Fedorov · 2017 to 2026
$6.0M
Integration of structure and signaling in cardiac pacemaker functionR01HL115580 · NHLBI · OHIO STATE UNIVERSITY · PI FEDOROV, VADIM V · 2013 to 2021
$4.2M
Integrated functional and structural mapping for targeting substrates of reentrant atrial fibrillation drivers in the human heartF30HL142179 · NHLBI · OHIO STATE UNIVERSITY · PI HANSEN, BRIAN J. · 2018 to 2021
$139k
NHLBI NIH HHS F30 HL142179NHLBI NIH HHS R01 HL115580NHLBI NIH HHS R01 HL135109
6 · The paper itself

Abstract

Atrial fibrillation (AF) is the most prevalent form of cardiac arrhythmia. The atrial wall thickness (AWT) can potentially improve our understanding of the mechanism underlying atrial structure that drives AF and provides important clinical information. However, most existing studies for estimating AWT rely on ruler-based measurements performed on only a few selected locations in 2D or 3D using digital calipers. Only a few studies have developed automatic approaches to estimate the AWT in the left atrium, and there are currently no methods to robustly estimate the AWT of both atrial chambers. Therefore, we have developed a computational pipeline to automatically calculate the 3D AWT across bi-atrial chambers and extensively validated our pipeline on both ex vivo and in vivo human atria data. The atrial geometry was first obtained by segmenting the atrial wall from the MRIs using a novel machine learning approach. The epicardial and endocardial surfaces were then separated using a multi-planar convex hull approach to define boundary conditions, from which, a Laplace equation was solved numerically to automatically separate bi-atrial chambers. To robustly estimate the AWT in each atrial chamber, coupled partial differential equations by coupling the Laplace solution with two surface trajectory functions were formulated and solved. Our pipeline enabled the reconstruction and visualization of the 3D AWT for bi-atrial chambers with a relative error of 8% and outperformed existing algorithms by >7%. Our approach can potentially lead to improved clinical diagnosis, patient stratification, and clinical guidance during ablation treatment for patients with AF.

Indexed as

AgedAlgorithmsFemaleHeart AtriaHumansImaging, Three-DimensionalMagnetic Resonance ImagingMaleMiddle AgedAtrial fibrillationAtrial wall thicknessHuman atriaLaplace solutionMRI

Identifiers

PMID31542646
PMCPMC6817405

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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.