Facilitating diabetic retinopathy screening using automated retinal image analysis in underresourced settings

被引:2
|
作者
Quinn, Nicola [1 ,2 ]
Brazionis, Laima [1 ,3 ]
Zhu, Benjamin [1 ]
Ryan, Chris [1 ,3 ]
D'Aloisio, Rossella [2 ,4 ]
Lilian Tang, Hongying [5 ]
Peto, Tunde [2 ]
Jenkins, Alicia [1 ,2 ,3 ]
机构
[1] Univ Sydney, NHMRC Clin Trials Ctr, Sydney, NSW, Australia
[2] Queens Univ, Ctr Publ Hlth, Belfast, Antrim, North Ireland
[3] Univ Melbourne, Dept Med, Melbourne, Vic, Australia
[4] Univ G dAnnunzio, Dept Med & Sci Ageing, Ophthalmol Clin, Chieti, Italy
[5] Univ Surrey, Dept Comp Sci, Guildford, Surrey, England
基金
英国医学研究理事会;
关键词
diabetic retinopathy; Indigenous Australians; automated retinal image analysis; VALIDATION; EYE;
D O I
10.1111/dme.14582
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim To evaluate an automated retinal image analysis (ARIA) of indigenous retinal fundus images against a human grading comparator for the classification of diabetic retinopathy (DR) status. Methods Indigenous Australian adults with type 2 diabetes (n = 410) from three remote and very remote primary-care services in the Northern Territory, Australia, underwent teleretinal DR screening. A single, central retinal fundus photograph (opportunistic mydriasis) for each eye was later regraded using a single ARIA and a UK human grader and national DR classification system. The sensitivity and specificity of ARIA were assessed relative to the comparator. Proportionate agreement and a Kappa statistic were also computed. Results Retinal images from 391 and 393 participants were gradable for 'Any DR' by the human grader and ARIA grader, respectively. 'Any DR' was detected by the human grader in 185 (47.3%) participants and by ARIA in 202 (48.6%) participants (agreement =88.0%, Kappa = 0.76,), whereas proliferative DR was detected in 31 (7.9%) and 37 (9.4%) participants (agreement = 98.2%, Kappa = 0.89,), respectively. The ARIA software had 91.4 (95% CI, 86.3-95.0) sensitivity and 85.0 (95% CI, 79.3-89.5) specificity for detecting 'Any DR' and 96.8 (95% CI, 83.3-99.9) sensitivity and 98.3 (95% CI, 96.4-99.4) specificity for detecting proliferative DR. Conclusions This ARIA software has high sensitivity for detecting 'Any DR', hence could be used as a triage tool for human graders. High sensitivity was also found for detection of proliferative DR by ARIA. Future versions of this ARIA should include maculopathy and referable DR (CSME and/or PDR). Such ARIA software may benefit diabetes care in less-resourced regions.
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页数:7
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