Validation and Clinical Applicability of Whole-Volume Automated Segmentation of Optical Coherence Tomography in Retinal Disease Using Deep Learning.


Journal

JAMA ophthalmology
ISSN: 2168-6173
Titre abrégé: JAMA Ophthalmol
Pays: United States
ID NLM: 101589539

Informations de publication

Date de publication:
01 Sep 2021
Historique:
pubmed: 9 7 2021
medline: 21 4 2022
entrez: 8 7 2021
Statut: ppublish

Résumé

Quantitative volumetric measures of retinal disease in optical coherence tomography (OCT) scans are infeasible to perform owing to the time required for manual grading. Expert-level deep learning systems for automatic OCT segmentation have recently been developed. However, the potential clinical applicability of these systems is largely unknown. To evaluate a deep learning model for whole-volume segmentation of 4 clinically important pathological features and assess clinical applicability. This diagnostic study used OCT data from 173 patients with a total of 15 558 B-scans, treated at Moorfields Eye Hospital. The data set included 2 common OCT devices and 2 macular conditions: wet age-related macular degeneration (107 scans) and diabetic macular edema (66 scans), covering the full range of severity, and from 3 points during treatment. Two expert graders performed pixel-level segmentations of intraretinal fluid, subretinal fluid, subretinal hyperreflective material, and pigment epithelial detachment, including all B-scans in each OCT volume, taking as long as 50 hours per scan. Quantitative evaluation of whole-volume model segmentations was performed. Qualitative evaluation of clinical applicability by 3 retinal experts was also conducted. Data were collected from June 1, 2012, to January 31, 2017, for set 1 and from January 1 to December 31, 2017, for set 2; graded between November 2018 and January 2020; and analyzed from February 2020 to November 2020. Rating and stack ranking for clinical applicability by retinal specialists, model-grader agreement for voxelwise segmentations, and total volume evaluated using Dice similarity coefficients, Bland-Altman plots, and intraclass correlation coefficients. Among the 173 patients included in the analysis (92 [53%] women), qualitative assessment found that automated whole-volume segmentation ranked better than or comparable to at least 1 expert grader in 127 scans (73%; 95% CI, 66%-79%). A neutral or positive rating was given to 135 model segmentations (78%; 95% CI, 71%-84%) and 309 expert gradings (2 per scan) (89%; 95% CI, 86%-92%). The model was rated neutrally or positively in 86% to 92% of diabetic macular edema scans and 53% to 87% of age-related macular degeneration scans. Intraclass correlations ranged from 0.33 (95% CI, 0.08-0.96) to 0.96 (95% CI, 0.90-0.99). Dice similarity coefficients ranged from 0.43 (95% CI, 0.29-0.66) to 0.78 (95% CI, 0.57-0.85). This deep learning-based segmentation tool provided clinically useful measures of retinal disease that would otherwise be infeasible to obtain. Qualitative evaluation was additionally important to reveal clinical applicability for both care management and research.

Identifiants

pubmed: 34236406
pii: 2781797
doi: 10.1001/jamaophthalmol.2021.2273
pmc: PMC8444027
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

964-973

Subventions

Organisme : Medical Research Council
ID : MR/T019050/1
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

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Auteurs

Marc Wilson (M)

Google Health, London, United Kingdom.

Reena Chopra (R)

Google Health, London, United Kingdom.
National Institute for Health Research Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital NHS (National Health Service) Foundation Trust, London, United Kingdom.
University College London Institute of Ophthalmology, London, United Kingdom.

Megan Z Wilson (MZ)

Google Health, London, United Kingdom.

Charlotte Cooper (C)

Google Health, London, United Kingdom.

Patricia MacWilliams (P)

Google Health, London, United Kingdom.

Yun Liu (Y)

Google Health, Palo Alto, California.

Ellery Wulczyn (E)

Google Health, Palo Alto, California.

Daniela Florea (D)

National Institute for Health Research Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital NHS (National Health Service) Foundation Trust, London, United Kingdom.
University College London Institute of Ophthalmology, London, United Kingdom.

Cían O Hughes (CO)

Google Health, London, United Kingdom.

Alan Karthikesalingam (A)

Google Health, London, United Kingdom.

Hagar Khalid (H)

National Institute for Health Research Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital NHS (National Health Service) Foundation Trust, London, United Kingdom.
University College London Institute of Ophthalmology, London, United Kingdom.

Sandra Vermeirsch (S)

National Institute for Health Research Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital NHS (National Health Service) Foundation Trust, London, United Kingdom.
University College London Institute of Ophthalmology, London, United Kingdom.

Luke Nicholson (L)

National Institute for Health Research Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital NHS (National Health Service) Foundation Trust, London, United Kingdom.
University College London Institute of Ophthalmology, London, United Kingdom.

Pearse A Keane (PA)

National Institute for Health Research Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital NHS (National Health Service) Foundation Trust, London, United Kingdom.
University College London Institute of Ophthalmology, London, United Kingdom.

Konstantinos Balaskas (K)

National Institute for Health Research Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital NHS (National Health Service) Foundation Trust, London, United Kingdom.
University College London Institute of Ophthalmology, London, United Kingdom.

Christopher J Kelly (CJ)

Google Health, London, United Kingdom.

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Classifications MeSH