A hybrid machine learning approach to localizing the origin of ventricular tachycardia using 12-lead electrocardiograms

Ryan Missel, Prashnna K. Gyawali, Jaideep Vitthal Murkute, Zhiyuan Li, Shijie Zhou, Amir AbdelWahab, Jason Davis, James Warren, John L. Sapp, Linwei Wang

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

18 Citas (Scopus)

Resumen

Background: Machine learning models may help localize the site of origin of ventricular tachycardia (VT) using 12-lead electrocardiograms. However, population-based models suffer from inter-subject anatomical variations within ECG data, while patient-specific models face the open challenge of what pacing data to collect for training. Methods: This study presents and validates the first hybrid model that combines population and patient-specific machine learning for rapid “computer-guided pace-mapping”. A population-based deep learning model was first trained offline to disentangle inter-subject variations and regionalize the site of VT origin. Given a new patient with a target VT, an on-line patient-specific model – after being initialized by the population-based prediction – was then built in real time by actively suggesting where to pace next and improving the prediction with each added pacing data, progressively guiding pace-mapping towards the site of VT origin. Results: The population model was trained on pace-mapping data from 38 patients and the patient-specific model was subsequently tuned on one patient. The resulting hybrid model was tested on a separate cohort of eight patients in localizing 1) 193 LV endocardial pacing sites, and 2) nine VTs with clinically determined exit sites. The hybrid model achieved a localization error of 5.3 ± 2.6 mm using 5.4 ± 2.5 pacing sites in localizing LV pacing sites, achieving a significantly higher accuracy with a significantly smaller amount of training sites in comparison to models without active guidance. Conclusion: The presented hybrid model has the potential to assist rapid pace-mapping of interventional targets in VT.

Idioma originalEnglish
Número de artículo104013
PublicaciónComputers in Biology and Medicine
Volumen126
DOI
EstadoPublished - nov. 2020

Nota bibliográfica

Funding Information:
This study was supported by grants from the National Institutes of Health under grant number R15HL140500 , the National Science Foundation under grant number ACI-1350374 , and the Cardiac Arrhythmia Network of Canada .

Funding Information:
Disclosure: Dr. Sapp has served as a consultant to Biosense Webster , has received research funding from Biosense and Abbott, has received speaker honoraria from Medtronic and Abbott, and has received patents for a needle ablation catheter (rights assigned, unlicensed) and for an automated VT localization algorithm (unlicensed).

Publisher Copyright:
© 2020 Elsevier Ltd

ASJC Scopus Subject Areas

  • Computer Science Applications
  • Health Informatics

PubMed: MeSH publication types

  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

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