Evidence map›Paper›PMID 33570241›Full record

ArticleJournal of cardiovascular electrophysiology2021

Novel mapping techniques for rotor core detection using simulated intracardiac electrograms.

Vasanth Ravikumar, Elizabeth Annoni, Preethy Parthiban, Sharon Zlochiver, Henri Roukoz, Siva K Mulpuru, Elena G Tolkacheva

Open access · greenAbstract read
In one paragraph

Article in Journal of cardiovascular electrophysiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Complexity analysis of electrical activity during endocardial and epicardial biventricular mapping of ventricular fibrillation.Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing · 2026
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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

7 authors at 3 institutions in 1 country.

Vasanth RavikumarDepartment of Electrical Engineering, University of Minnesota, Minneapolis, Minnesota, USA.ORCID 0000-0002-8959-3214
Elizabeth AnnoniDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota, USA.
Preethy ParthibanDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota, USA.
Sharon ZlochiverDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota, USA.
Henri RoukozDivision of Cardiovascular, Medical School, University of Minnesota, Minneapolis, Minnesota, USA.ORCID 0000-0002-8011-0829
Siva K MulpuruDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-7694-3617
Elena G TolkachevaDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota, USA.ORCID 0000-0003-1624-5793
University of Minnesota · USMayo Clinic · USUniversity of Minnesota Medical Center · US

Funding

Unfolded Protein Response and ArrhythmiasR01HL134791 · NHLBI · UNIVERSITY OF MINNESOTA · PI DUDLEY, SAMUEL C · 2017 to 2020
$1.8M
NHLBI NIH HHS R01 HL134791
6 · The paper itself

Abstract

backgroundCatheter ablation is associated with limited success rates in patients with persistent atrial fibrillation (AF). Currently, existing mapping systems fail to identify critical target sites for ablation. Recently, we proposed and validated several techniques (multiscale frequency [MSF], Shannon entropy [SE], kurtosis [Kt], and multiscale entropy [MSE]) to identify pivot point of rotors using ex-vivo optical mapping animal experiments. However, the performance of these techniques is unclear for the clinically recorded intracardiac electrograms (EGMs), due to the different nature of the signals.

objectiveThis study aims to evaluate the performance of MSF, MSE, SE, and Kt techniques to identify the pivot point of the rotor using unipolar and bipolar EGMs obtained from numerical simulations.

methodsStationary and meandering rotors were simulated in a 2D human atria. The performances of new approaches were quantified by comparing the "true" core of the rotor with the core identified by the techniques. Also, the performances of all techniques were evaluated in the presence of noise, scar, and for the case of the multielectrode multispline and grid catheters.

resultsOur results demonstrate that all the approaches are able to accurately identify the pivot point of both stationary and meandering rotors from both unipolar and bipolar EGMs. The presence of noise and scar tissue did not significantly affect the performance of the techniques. Finally, the core of the rotors was correctly identified for the case of multielectrode multispline and grid catheter simulations.

conclusionThe core of rotors can be successfully identified from EGMs using novel techniques; thus, providing motivation for future clinical implementations.

Indexed as

Atrial FibrillationCatheter AblationAnimalsElectrophysiologic Techniques, CardiacEntropyHeart AtriaHumansatrial fibrillationclinical limitationskurtosismultiscale entropymultiscale frequencyrotorsShannon entropysimulated intracardiac electrograms

Identifiers

PMID33570241
PMCPMC8119376
OpenAlexW3127856355

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.