Evidence map›Paper›PMID 36369980›Full record

ArticleEuropace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology2023

Non-invasive localization of post-infarct ventricular tachycardia exit sites to guide ablation planning: a computational deep learning platform utilizing the 12-lead electrocardiogram and intracardiac electrograms from implanted devices.

Sofia Monaci, Shuang Qian, Karli Gillette, Esther Puyol-Antón, Rahul Mukherjee, Mark K Elliott, John Whitaker, Ronak Rajani, Mark O'Neill, Christopher A Rinaldi and 3 more

Open access · hybridAbstract read
In one paragraph

Article in 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, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Value of the 12-lead ECG to localize the origin of ventricular tachycardia.Herzschrittmachertherapie & Elektrophysiologie · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Computational modelling of biological systems now and then: revisiting tools and visions from the beginning of the century.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2025
    Review
  8. Article
  9. Review
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  11. Review
  12. Managing arrhythmia in cardiac resynchronisation therapy.Frontiers in cardiovascular medicine · 2023
    Review
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

13 authors at 3 institutions in 2 countries.

Sofia MonaciBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-6786-5215
Shuang QianBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-2313-0268
Karli GilletteMedical University of Graz, Graz 8036, Austria.ORCID 0000-0002-0420-5375
Esther Puyol-AntónBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-9789-6629
Rahul MukherjeeBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-6462-8740
Mark K ElliottBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0003-2805-3043
John WhitakerBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-5361-5725
Ronak RajaniBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-8816-6296
Mark O'NeillBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-6070-7177
Christopher A RinaldiBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-3930-1957
Gernot PlankMedical University of Graz, Graz 8036, Austria.ORCID 0000-0002-7380-6908
Andrew P KingBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-9965-7015
Martin J BishopBiomedical Engineering & Imaging Sciences, King's College London, London SE1 7EH, United Kingdom.ORCID 0000-0002-6237-1902
King's College London · GBSt Thomas' Hospital · GBMedical University of Graz · AT

Funding

British Heart Foundation PG/22/10871Medical Research Council MR/N011007/1Wellcome Trust
6 · The paper itself

Abstract

aimsExisting strategies that identify post-infarct ventricular tachycardia (VT) ablation target either employ invasive electrophysiological (EP) mapping or non-invasive modalities utilizing the electrocardiogram (ECG). Their success relies on localizing sites critical to the maintenance of the clinical arrhythmia, not always recorded on the 12-lead ECG. Targeting the clinical VT by utilizing electrograms (EGM) recordings stored in implanted devices may aid ablation planning, enhancing safety and speed and potentially reducing the need of VT induction. In this context, we aim to develop a non-invasive computational-deep learning (DL) platform to localize VT exit sites from surface ECGs and implanted device intracardiac EGMs. METHODS AND

resultsA library of ECGs and EGMs from simulated paced beats and representative post-infarct VTs was generated across five torso models. Traces were used to train DL algorithms to localize VT sites of earliest systolic activation; first tested on simulated data and then on a clinically induced VT to show applicability of our platform in clinical settings. Localization performance was estimated via localization errors (LEs) against known VT exit sites from simulations or clinical ablation targets. Surface ECGs successfully localized post-infarct VTs from simulated data with mean LE = 9.61 ± 2.61 mm across torsos. VT localization was successfully achieved from implanted device intracardiac EGMs with mean LE = 13.10 ± 2.36 mm. Finally, the clinically induced VT localization was in agreement with the clinical ablation volume.

conclusionThe proposed framework may be utilized for direct localization of post-infarct VTs from surface ECGs and/or implanted device EGMs, or in conjunction with efficient, patient-specific modelling, enhancing safety and speed of ablation planning.

Indexed as

Catheter AblationDeep LearningTachycardia, VentricularElectrocardiographyElectrophysiologic Techniques, CardiacHumansInfarctionComputational modellingDeep learningElectrocardiogramImplanted device electrogramsNon-invasive VT localizationPre-procedure planning

Identifiers

PMID36369980
PMCPMC9935046
OpenAlexW4308834610

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.