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Automated Diabetic Retinopathy Image Assessment Software: Diagnostic Accuracy and Cost-Effectiveness Compared with Human Graders.

Tufail, A; Rudisill, C; Egan, C; Kapetanakis, VV; Salas-Vega, S; Owen, CG; Lee, A; Louw, V; Anderson, J; Liew, G; et al. Tufail, A; Rudisill, C; Egan, C; Kapetanakis, VV; Salas-Vega, S; Owen, CG; Lee, A; Louw, V; Anderson, J; Liew, G; Bolter, L; Srinivas, S; Nittala, M; Sadda, S; Taylor, P; Rudnicka, AR (2017) Automated Diabetic Retinopathy Image Assessment Software: Diagnostic Accuracy and Cost-Effectiveness Compared with Human Graders. Ophthalmology, 124 (3). pp. 343-351. ISSN 1549-4713 https://doi.org/10.1016/j.ophtha.2016.11.014
SGUL Authors: Owen, Christopher Grant Rudnicka, Alicja Regina

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Abstract

OBJECTIVE: With the increasing prevalence of diabetes, annual screening for diabetic retinopathy (DR) by expert human grading of retinal images is challenging. Automated DR image assessment systems (ARIAS) may provide clinically effective and cost-effective detection of retinopathy. We aimed to determine whether ARIAS can be safely introduced into DR screening pathways to replace human graders. DESIGN: Observational measurement comparison study of human graders following a national screening program for DR versus ARIAS. PARTICIPANTS: Retinal images from 20 258 consecutive patients attending routine annual diabetic eye screening between June 1, 2012, and November 4, 2013. METHODS: Retinal images were manually graded following a standard national protocol for DR screening and were processed by 3 ARIAS: iGradingM, Retmarker, and EyeArt. Discrepancies between manual grades and ARIAS results were sent to a reading center for arbitration. MAIN OUTCOME MEASURES: Screening performance (sensitivity, false-positive rate) and diagnostic accuracy (95% confidence intervals of screening-performance measures) were determined. Economic analysis estimated the cost per appropriate screening outcome. RESULTS: Sensitivity point estimates (95% confidence intervals) of the ARIAS were as follows: EyeArt 94.7% (94.2%-95.2%) for any retinopathy, 93.8% (92.9%-94.6%) for referable retinopathy (human graded as either ungradable, maculopathy, preproliferative, or proliferative), 99.6% (97.0%-99.9%) for proliferative retinopathy; Retmarker 73.0% (72.0 %-74.0%) for any retinopathy, 85.0% (83.6%-86.2%) for referable retinopathy, 97.9% (94.9%-99.1%) for proliferative retinopathy. iGradingM classified all images as either having disease or being ungradable. EyeArt and Retmarker saved costs compared with manual grading both as a replacement for initial human grading and as a filter prior to primary human grading, although the latter approach was less cost-effective. CONCLUSIONS: Retmarker and EyeArt systems achieved acceptable sensitivity for referable retinopathy when compared with that of human graders and had sufficient specificity to make them cost-effective alternatives to manual grading alone. ARIAS have the potential to reduce costs in developed-world health care economies and to aid delivery of DR screening in developing or remote health care settings.

Item Type: Article
Additional Information: © 2016 by the American Academy of Ophthalmology This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). Published by Elsevier Inc.
Keywords: Ophthalmology & Optometry, 1103 Clinical Sciences, 1113 Ophthalmology And Optometry, 1117 Public Health And Health Services
SGUL Research Institute / Research Centre: Academic Structure > Population Health Research Institute (INPH)
Journal or Publication Title: Ophthalmology
ISSN: 1549-4713
Language: eng
Dates:
DateEvent
23 December 2016Published Online
10 November 2016Accepted
1 March 2017Published
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
Projects:
Project IDFunderFunder ID
11/21/02National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
PubMed ID: 28024825
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/108379
Publisher's version: https://doi.org/10.1016/j.ophtha.2016.11.014

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