An artificial intelligence tool for automated analysis of large-scale unstructured clinical cine cardiac magnetic resonance databases

Author:

Mariscal-Harana Jorge1,Asher Clint12,Vergani Vittoria1,Rizvi Maleeha12,Keehn Louise3ORCID,Kim Raymond J4,Judd Robert M4,Petersen Steffen E5678ORCID,Razavi Reza12ORCID,King Andrew P1ORCID,Ruijsink Bram129,Puyol-Antón Esther1ORCID

Affiliation:

1. School of Biomedical Engineering & Imaging Sciences Rayne Institute , 4th Floor, Lambeth Wing St. Thomas' Hospital Westminster Bridge Road London SE1 7EH

2. Department of Adult and Paediatric Cardiology, Guy’s and St Thomas’ NHS Foundation Trust , Westminster Bridge Road, London SE1 7EH, London , UK

3. Department of Clinical Pharmacology, King’s College London British Heart Foundation Centre, St Thomas’ Hospital , London, Westminster Bridge Road, London SE1 7EH , UK

4. Division of Cardiology, Department of Medicine, Duke University , 40 Duke Medicine Circle, Durham, NC 27710 , USA

5. William Harvey Research Institute, NIHR Barts Biomedical Research Centre, Queen Mary University of London , Charterhouse Square, London EC1M 6BQ , UK

6. Barts Heart Centre, St Bartholomew’s Hospital, Barts Health NHS Trust , W Smithfield, London EC1A 7BE , UK

7. Health Data Research UK , Gibbs Building, 215 Euston Rd., London NW1 2BE , UK

8. Alan Turing Institute , 96 Euston Rd., London NW1 2DB , UK

9. Department of Cardiology, Division Heart and Lungs, University Medical Center Utrecht, Utrecht University , 3584 CX Utrecht , the Netherlands

Abstract

Abstract Aims Artificial intelligence (AI) techniques have been proposed for automating analysis of short-axis (SAX) cine cardiac magnetic resonance (CMR), but no CMR analysis tool exists to automatically analyse large (unstructured) clinical CMR datasets. We develop and validate a robust AI tool for start-to-end automatic quantification of cardiac function from SAX cine CMR in large clinical databases. Methods and results Our pipeline for processing and analysing CMR databases includes automated steps to identify the correct data, robust image pre-processing, an AI algorithm for biventricular segmentation of SAX CMR and estimation of functional biomarkers, and automated post-analysis quality control to detect and correct errors. The segmentation algorithm was trained on 2793 CMR scans from two NHS hospitals and validated on additional cases from this dataset (n = 414) and five external datasets (n = 6888), including scans of patients with a range of diseases acquired at 12 different centres using CMR scanners from all major vendors. Median absolute errors in cardiac biomarkers were within the range of inter-observer variability: <8.4 mL (left ventricle volume), <9.2 mL (right ventricle volume), <13.3 g (left ventricular mass), and <5.9% (ejection fraction) across all datasets. Stratification of cases according to phenotypes of cardiac disease and scanner vendors showed good performance across all groups. Conclusion We show that our proposed tool, which combines image pre-processing steps, a domain-generalizable AI algorithm trained on a large-scale multi-domain CMR dataset and quality control steps, allows robust analysis of (clinical or research) databases from multiple centres, vendors, and cardiac diseases. This enables translation of our tool for use in fully automated processing of large multi-centre databases.

Funder

EPSRC

Advancing Impact Award scheme of the Impact Acceleration Account

Wellcome/EPSRC Centre for Medical Engineering

National Institute for Health Research

Cardiovascular MedTech Co-operative award

NIHR comprehensive Biomedical Research Centre

British Heart Foundation

NIHR Biomedical Research Centre

European Union’s Horizon 2020 Research and Innovation Programme

CAP-AI Programme

European Regional Development Fund and Barts Charity

UK Research and Innovation

Publisher

Oxford University Press (OUP)

Subject

Energy Engineering and Power Technology,Fuel Technology

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