Machine learning in sudden cardiac death risk prediction: a systematic review

Author:

Barker Joseph12ORCID,Li Xin13ORCID,Khavandi Sarah4ORCID,Koeckerling David5,Mavilakandy Akash1,Pepper Coral6ORCID,Bountziouka Vasiliki1,Chen Long7ORCID,Kotb Ahmed12ORCID,Antoun Ibrahim1ORCID,Mansir John8ORCID,Smith-Byrne Karl9ORCID,Schlindwein Fernando S13ORCID,Dhutia Harshil12,Tyukin Ivan10ORCID,Nicolson William B12,Ng G Andre1211ORCID

Affiliation:

1. Department of Cardiovascular Sciences, University of Leicester , Leicester , UK

2. Cardiology Department, Glenfield Hospital, University Hospitals Leicester , Leicester , UK

3. School of Engineering, University of Leicester , Leicester , UK

4. Faculty of Medicine, Imperial College School of Medicine, Imperial College London , London , UK

5. Division of Angiology, Swiss Cardiovascular Center, Inselspital, Bern University Hospital, University of Bern , Bern , Switzerland

6. Library and Information Service, University Hospitals of Leicester NHS Trust , Leicester , UK

7. School of Computing and Mathematical Sciences, University of Leicester , Leicester , UK

8. Independent Scholar , London , UK

9. Cancer Epidemiology Unit, Nuffield Department of Population Health, University of Oxford , Oxford , UK

10. Department of Mathematics, University of Leicester , Leicester , UK

11. Cardiovascular Theme, National Institute for Health Research, Leicester Biomedical Research Centre , Leicester , UK

Abstract

Abstract Aims Most patients who receive implantable cardioverter defibrillators (ICDs) for primary prevention do not receive therapy during the lifespan of the ICD, whilst up to 50% of sudden cardiac death (SCD) occur in individuals who are considered low risk by conventional criteria. Machine learning offers a novel approach to risk stratification for ICD assignment. Methods and results Systematic search was performed in MEDLINE, Embase, Emcare, CINAHL, Cochrane Library, OpenGrey, MedrXiv, arXiv, Scopus, and Web of Science. Studies modelling SCD risk prediction within days to years using machine learning were eligible for inclusion. Transparency and quality of reporting (TRIPOD) and risk of bias (PROBAST) were assessed. A total of 4356 studies were screened with 11 meeting the inclusion criteria with heterogeneous populations, methods, and outcome measures preventing meta-analysis. The study size ranged from 122 to 124 097 participants. Input data sources included demographic, clinical, electrocardiogram, electrophysiological, imaging, and genetic data ranging from 4 to 72 variables per model. The most common outcome metric reported was the area under the receiver operator characteristic (n = 7) ranging between 0.71 and 0.96. In six studies comparing machine learning models and regression, machine learning improved performance in five. No studies adhered to a reporting standard. Five of the papers were at high risk of bias. Conclusion Machine learning for SCD prediction has been under-applied and incorrectly implemented but is ripe for future investigation. It may have some incremental utility in predicting SCD over traditional models. The development of reporting standards for machine learning is required to improve the quality of evidence reporting in the field.

Funder

NIHR

British Heart Foundation Programme

Medical Research Council Biomedical Catalyst Developmental Pathway Funding Scheme

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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