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Deep learning in congenital heart disease imaging: hope but not haste
  1. Rhodri Davies1,2,
  2. Sonya V Babu-Narayan3,4
  1. 1 Barts Heart Centre, St Bartholomew's Hospital, London, UK
  2. 2 Institute of Cardiovascular Science, University College London, London, London, UK
  3. 3 Adult Congenital Heart Centre and National Centre for Pulmonary Hypertension, Royal Brompton Hospital, London, UK
  4. 4 National Heart and Lung Institute, Imperial College, London, UK
  1. Correspondence to Dr Rhodri Davies, Barts Health NHS Trust, London E1 1BB, UK; rhodri.davies2{at}nhs.net

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Deep learning promises to revolutionise cardiac imaging with more accurate and more reproducible interpretation delivered almost instantaneously. But transferring promise into clinical delivery is a considerable task and we lag behind other fields.

The growing demand for cardiac imaging due to an ageing population with growing disease burden is not matched by an increased supply of clinicians trained in image interpretation. This is exacerbated in congenital heart disease due to increasing survivorship, disease complexity and paucity of available expertise. Deep learning has revolutionised the field of image analysis and there are now systems capable of automating cardiac image segmentation. Eliminating tedious tasks such as measuring structures on images can reduce burn-out and refocus clinicians on higher-level functions, the doctor–patient relationship and providing more empathic care.

But deep learning promises much more: it has the potential to improve on expert human image interpretation, and this is being realised with reports of better-than-human performance for breast cancer detection.1 We, as clinical experts, are not as good as we think we are at image interpretation—the minimal detectable change when ejection fraction is measured by an expert on cardiac MRI is 8.7%, mostly due to poor repeatability.2 Deep learning has potential for more accurate and more precise analysis where confidence in reported results can be quantified. Benefits could cascade through healthcare systems, with fewer repeated tests, less follow-up, and ultimately better clinical outcomes.

Cheap hardware and easy-to-use open-source software have made deep …

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Footnotes

  • Contributors RD and SVB-N coauthored the paper, with RD leading the technical and SVB-N leading the clinical aspects.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

  • Patient consent for publication Not required.

  • Provenance and peer review Commissioned; internally peer reviewed.

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