Abstract

The volume and complexity of diagnostic imaging is increasing at a pace faster than the availability of human expertise to interpret it. Artificial intelligence has shown great promise in classifying two-dimensional photographs of some common diseases and typically relies on databases of millions of annotated images. Until now, the challenge of reaching the performance of expert clinicians in a real-world clinical pathway with three-dimensional diagnostic scans has remained unsolved. Here, we apply a novel deep learning architecture to a clinically heterogeneous set of three-dimensional optical coherence tomography scans from patients referred to a major eye hospital. We demonstrate performance in making a referral recommendation that reaches or exceeds that of experts on a range of sight-threatening retinal diseases after training on only 14,884 scans. Moreover, we demonstrate that the tissue segmentations produced by our architecture act as a device-independent representation; referral accuracy is maintained when using tissue segmentations from a different type of device. Our work removes previous barriers to wider clinical use without prohibitive training data requirements across multiple pathologies in a real-world setting.

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Acknowledgements

We thank K. Kavukcuoglu, A. Zisserman, M. Jaderberg, K. Simonyan for discussions, A. Cain and M. Cant for work on the visuals, D. Mitchell and M. Johnson for infrastructure and systems administration, J. Morgan and OpenEyes for providing the electronic health record records, T. Peto, P. Blows, A. O’Shea and the NIHR Clinical Research Facility for work on the labeling, T. Heeran, M. Lukic, K. Kortum, K. Fasler, S. Wagner and N. Pontikos for work on the labeling, E. Steele, V. Louw, S. Gill and the rest of Moorfields IT team for work on the data collection and deidentification, S. Al-Abed and N. Smith for Moorfields technical advice at project initiation, R. Wood and D. Corder at Softwire for engineering support at Moorfields, R. Ogbe and the Moorfields Information Governance team for support, M. Hassard for Moorfields research and development support, K. Bonstein and the National Institute for Health Research (NIHR) for support at the Moorfields Biomedical Research Centre (BRC), J. Besley for legal assistance, E. Manna for patient engagement and support, and the rest of the DeepMind team for their support, ideas and encouragement. P.A.K. is supported by an NIHR Clinician Scientist Award (NIHR-CS-2014-14-023). D.A.S., A.T., C.E. and P.T.K. are supported by the NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology and the NIHR Moorfields Clinical Research Facility. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. R.C. receives studentship support from the College of Optometrists, United Kingdom.

Author information

Author notes

    • Julien Cornebise

    Present address: University College London, London, UK

  1. These authors contributed equally: Julien Cornebise, Pearse A. Keane, Olaf Ronneberger.

Affiliations

  1. DeepMind, London, UK

    • Jeffrey De Fauw
    • , Joseph R. Ledsam
    • , Bernardino Romera-Paredes
    • , Stanislav Nikolov
    • , Nenad Tomasev
    • , Sam Blackwell
    • , Harry Askham
    • , Xavier Glorot
    • , Brendan O’Donoghue
    • , Daniel Visentin
    • , George van den Driessche
    • , Balaji Lakshminarayanan
    • , Clemens Meyer
    • , Faith Mackinder
    • , Simon Bouton
    • , Kareem Ayoub
    • , Dominic King
    • , Alan Karthikesalingam
    • , Cían O. Hughes
    • , Demis Hassabis
    • , Trevor Back
    • , Mustafa Suleyman
    • , Julien Cornebise
    •  & Olaf Ronneberger
  2. NIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK

    • Reena Chopra
    • , Julian Hughes
    • , Dawn A. Sim
    • , Catherine Egan
    • , Adnan Tufail
    • , Peng T. Khaw
    •  & Pearse A. Keane

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Contributions

P.A.K., M.S., J.C., D.H., P.T.K., T.B. and K.A. initiated the project and the collaboration. O.R., J.D.F., B.R.-P. and S.N. developed the network architectures, training and testing setup. P.A.K., J.R.L. and R.C. designed the clinical setup. P.A.K., J.R.L., J.C., R.C., D.A.S., C.E. and A.T. created the dataset and defined clinical labels. J.D.F., B.R.-P., S.N., N.T., S.Bl., H.A., B.O., D.V., G.v.d.D., O.R. and J.C. contributed to the software engineering. J.R.L., S.Bl. and H.A. created the database. P.A.K., J.R.L., D.K., A.K., C.O.H. and R.R. contributed clinical expertise. O.R., P.A.K., J.D.F., J.R.L., B.R.-P., S.N., N.T. and X.G. analysed the data. T.B., S.Bo., J.C., J.H., F.M. and C.M. managed the project. O.R., P.A.K., J.R.L., J.D.F., B.R.-P., G.R. and H.M. wrote the paper. B.L. contributed to the uncertainty estimation.

Competing interests

P.A.K., G.R., H.M. and R.R. are paid contractors of DeepMind. P.A.K. has received speaker fees from Heidelberg Engineering, Topcon, Haag-Streit, Allergan, Novartis and Bayer. P.A.K. has served on advisory boards for Novartis and Bayer, and is an external consultant for DeepMind and Optos. A.T. has served on advisory boards for the following companies: Allergan, Bayer, Genentech, GlaxoSmithKline, Novartis, Roche. C.E. has received speaker fees from Heidelberg Engineering and Haag-Streit UK. P.T.K. has served on advisory boards for Aerie, Allergan, Alcon, Belkin Laser, Novartis and Santen. D.A.S. has received speaker fees from Novartis, Bayer, Allergan, Haag-Streit. The authors have no other competing interests to disclose.

Corresponding authors

Correspondence to Pearse A. Keane or Olaf Ronneberger.

Supplementary Information

  1. Supplementary Text and Figures

    Supplementary Figures 1–16 and Supplementary Tables 1–10

  2. Reporting Summary

  3. Supplementary Video 1

    OCT viewer | This video demonstrates the interaction with the OCT viewer. The OCT scan belongs to a 72 year old female presented with increasing visual distortion over a 4 month period; the OCT shows loss of RPE consistent with geographic atrophy. The view first goes through the whole volume (128 slices) for a fixed tissue map hypothesis, followed by showing the different tissue map hypotheses for a given slice. Finally, we let the collage cycle through the different hypotheses continually while scrolling through the volume, pausing on several slices briefly to show the variations. The color legend for all segmentation maps is available in Supplementary Table 2.

  4. Supplementary Video 2

    Wet AMD | Choroidal neovascularization (CNV) is the pathognomonic feature of the neovascular (“wet”) form of age-related macular degeneration (AMD) and requires urgent treatment to prevent irreversible visual loss. A 72-year old man presented with a history of reduced vision in his left eye. Best corrected visual acuity in the affected eye was 38 Early Treatment Diabetic Retinopathy Study (ETDRS) letters. The model correctly selects the Most Urgent Diagnosis as “CNV”, suggesting referral to an ophthalmologist on an urgent basis. The model segmentation highlights growth of the neovascular tissue in the sub-retinal pigment epithelium (RPE) space – a so-called fibrovascular pigment epithelium detachment (PED). Subretinal fluid can be seen surrounding the inferior margins of the fibrovascular PED indicating the presence of ongoing CNV leakage.

  5. Supplementary Video 3

    Normal | Scans are quick and safe to perform and are thus commonly used in the screening of patients without visual symptoms or other ophthalmic findings. A 46-year old man who was referred for retinal specialist review. Best corrected visual acuity was 6/6. The model correctly selects the referral decision as “Observation Only”, suggesting that the OCT findings in isolation do not require referral to an ophthalmologist. The model accurately delineates the neurosensory retina without the presence of any pathologic compartments. It also highlights partial separation of the posterior hyaloid of the vitreous – this is a normal finding as the vitreous gel increasingly liquefies with age.

  6. Supplementary Video 4

    Diabetic macular edema | Accumulation of this fluid in the macula – diabetic macular edema (DME) – is the commonest cause of visual impairment in diabetes. A 54-year old man with diabetes was referred to Moorfields for ophthalmologist review with best corrected visual acuity in the affected eye of 45 ETDRS letters. The model correctly detects the presence of macular retinal edema (MRE) and suggests semi-urgent ophthalmology referral. The model highlights intraretinal fluid accumulation, with cystoid spaces in both the inner nuclear and outer plexiform layers, and a mixed petaloid/honeycomb appearance on the en face images. There is also an accompanying significant increase in total retinal thickness.

  7. Supplementary Video 5

    Ambiguous case (chronic central serous retinopathy) | In chronic CSR, diagnosis of secondary CNV formation is often challenging due to the frequent presence of shallow irregular pigment epithelium detachments (PEDs). A 60-64 year old woman presented with a history of CSR in her left eye. The model correctly detects the presence of CSR but is far less certain about the presence of CNV. It highlights a gravitational tract of subretinal fluid with a discrete area of fibrovascular PED superior to the fovea.

  8. Supplementary Video 6

    Ambiguous case (advanced geographic atrophy) | In advanced forms of AMD, geographic atrophy (GA) may sometimes coexist with CNV formation. In such cases, the CNV component may be clinically silent, and the fundus appearance may be limited to that of GA, making the diagnosis difficult. A 84-year old man was referred to Moorfields. Best corrected visual acuity in the affected eye was 1/60. The ground truth diagnosis was GA and routine referral was recommended. While the model correctly diagnoses the presence of GA and drusen, it suggests urgent referral due to the possible presence of CNV. The presence of subretinal hyperreflective on model segmentation is suggestive of previous CNV formation.

  9. Supplementary Video 7

    Difficult case of choroidal neovascularization | A 30 year old male patient, with a known history of CSR, presented with acute visual loss in his left eye and was diagnosed with secondary CNV formation. At this visit, the OCT scans lack many of the prototypical features of CSR, such as subretinal fluid accumulation. The model correctly diagnoses the presence of CNV and suggests the presence of CSR, but with far less certainty.

  10. Supplementary Video 8

    Failure case (partial-thickness macular hole) | Ocular media opacities may sometimes cause artefactual reductions in OCT signal strength and this can make accurate image segmentation challenging. Due to localized reduction in OCT signal strength in this case, some of the models erroneously detect the presence of a partial thickness macular hole. As a result, the models are uncertain as to whether the eye is normal or whether routine referral is required.

  11. Supplementary Video 9

    Integration with other clinical information | Retinal angiomatous proliferation (RAP) is a variant of choroidal neovascularization (CNV) due to age-related macular degeneration (AMD). A 75-79 year old woman presented with reduced vision in her left eye. The model segmentation highlights the presence of a fibrovascular pigment epithelium detachment (PED) with subretinal hyperreflective material, overlying intraretinal fluid, and surrounding drusen. These findings are highly suggestive of RAP - in its early stages, this can be misdiagnosed as macular retinal edema (MRE), particularly in elderly patients with diabetes. The interpretable representation reduces the risk of misdiagnosis and allows the clinician to easily correlate these findings with other clinical information, e.g., fundus fluorescein angiography.

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https://doi.org/10.1038/s41591-018-0107-6

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