Gilbert Lim

Dr. Gilbert Lim

School of Computing, National University of Singapore, Singapore
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 December 2017 in JAMA
Verified
Journal Article
Open access
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DTDaniel Shu Wei Ting
Daniel Shu Wei Ting
CCCarol Yim-Lui Cheung
Carol Yim-Lui Cheung
GLGilbert Lim
Gilbert Lim
GTGavin Siew Wei Tan
Gavin Siew Wei Tan
NQNguyen D. Quang
Nguyen D. Quang
TWTien Yin Wong
Tien Yin Wong
By 2040, it is projected that approximately 600 million people will have diabetes, with one-third expected to have diabetic retinopathy.1-3 Screening for diabetic retinopathy, coupled with timely referral and treatment, is a universally accepted strategy for blindness prevention.2 However, programs for screening diabetic retinopathy are challenged by issues related to implementation, availability of human assessors, and long-term financial sustainability.2,4-7

1 May 2019 in The Lancet Digital Health
Verified
Journal Article
Open access
VBValentina Bellemo
Valentina Bellemo
ZLZhan W Lim
Zhan W Lim
GLGilbert Lim
Gilbert Lim
QNQuang D Nguyen
Quang D Nguyen
YXYuchen Xie
Yuchen Xie
DTDarren Shu Jeng Ting
Darren Shu Jeng Ting
Radical measures are required to identify and reduce blindness due to diabetes to achieve the Sustainable Development Goals by 2030. Therefore, we evaluated the accuracy of an artificial intelligence (AI) model using deep learning in a population-based diabetic retinopathy screening programme in Zambia, a lower-middle-income country. We adopted an ensemble AI model consisting of a combination of two convolutional neural networks (an adapted VGGNet architecture and a residual neural network architecture) for classifying retinal colour fundus images. We trained our model on 76 370 retinal fundus images from 13 099 patients with diabetes who had participated in the Singapore Integrated Diabetic Retinopathy Program, between 2010 and 2013, which has been published previously. In this clinical validation study, we included all patients with a diagnosis of diabetes that attended a mobile screening unit in five urban centres in the Copperbelt province of Zambia from Feb 1 to June 31, 2012. In our model, referable diabetic retinopathy was defined as moderate non-proliferative diabetic retinopathy or worse, diabetic macular oedema, and ungradable images. Vision-threatening diabetic retinopathy comprised severe non-proliferative and proliferative diabetic retinopathy. We calculated the area under the curve (AUC), sensitivity, and specificity for referable diabetic retinopathy, and sensitivities of vision-threatening diabetic retinopathy and diabetic macular oedema compared with the grading by retinal specialists. We did a multivariate analysis for systemic risk factors and referable diabetic retinopathy between AI and human graders. A total of 4504 retinal fundus images from 3093 eyes of 1574 Zambians with diabetes were prospectively recruited. Referable diabetic retinopathy was found in 697 (22·5%) eyes, vision-threatening diabetic retinopathy in 171 (5·5%) eyes, and diabetic macular oedema in 249 (8·1%) eyes. The AUC of the AI system for referable diabetic retinopathy was 0·973 (95% CI 0·969-0·978), with corresponding sensitivity of 92·25% (90·10-94·12) and specificity of 89·04% (87·85-90·28). Vision-threatening diabetic retinopathy sensitivity was 99·42% (99·15-99·68) and diabetic macular oedema sensitivity was 97·19% (96·61-97·77). The AI model and human graders showed similar outcomes in referable diabetic retinopathy prevalence detection and systemic risk factors associations. Both the AI model and human graders identified longer duration of diabetes, higher level of glycated haemoglobin, and increased systolic blood pressure as risk factors associated with referable diabetic retinopathy. An AI system shows clinically acceptable performance in detecting referable diabetic retinopathy, vision-threatening diabetic retinopathy, and diabetic macular oedema in population-based diabetic retinopathy screening. This shows the potential application and adoption of such AI technology in an under-resourced African population to reduce the incidence of preventable blindness, even when the model is trained in a different population. National Medical Research Council Health Service Research Grant, Large Collaborative Grant, Ministry of Health, Singapore; the SingHealth Foundation; and the Tanoto Foundation.

5 September 2019 in Eye
Verified
Journal Article
Closed access
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Andrzej GrzybowskiAndrzej Grzybowski
Andrzej Grzybowski
PBPiotr Brona
Piotr Brona
GLGilbert Lim
Gilbert Lim
PRPaisan Ruamviboonsuk
Paisan Ruamviboonsuk
GTGavin S. W. Tan
Gavin S. W. Tan
DTDarren Shu Jeng Ting
Darren Shu Jeng Ting

1 May 2020 in The Lancet Digital Health
Verified
Journal Article
Open access
YXYuchen Xie
Yuchen Xie
QNQuang D Nguyen
Quang D Nguyen
HHHaslina Hamzah
Haslina Hamzah
GLGilbert Lim
Gilbert Lim
VBValentina Bellemo
Valentina Bellemo
DTDarren Shu Jeng Ting
Darren Shu Jeng Ting
Deep learning is a novel machine learning technique that has been shown to be as effective as human graders in detecting diabetic retinopathy from fundus photographs. We used a cost-minimisation analysis to evaluate the potential savings of two deep learning approaches as compared with the current human assessment: a semi-automated deep learning model as a triage filter before secondary human assessment; and a fully automated deep learning model without human assessment. In this economic analysis modelling study, using 39 006 consecutive patients with diabetes in a national diabetic retinopathy screening programme in Singapore in 2015, we used a decision tree model and TreeAge Pro to compare the actual cost of screening this cohort with human graders against the simulated cost for semi-automated and fully automated screening models. Model parameters included diabetic retinopathy prevalence rates, diabetic retinopathy screening costs under each screening model, cost of medical consultation, and diagnostic performance (ie, sensitivity and specificity). The primary outcome was total cost for each screening model. Deterministic sensitivity analyses were done to gauge the sensitivity of the results to key model assumptions. From the health system perspective, the semi-automated screening model was the least expensive of the three models, at US$62 per patient per year. The fully automated model was $66 per patient per year, and the human assessment model was $77 per patient per year. The savings to the Singapore health system associated with switching to the semi-automated model are estimated to be $489 000, which is roughly 20% of the current annual screening cost. By 2050, Singapore is projected to have 1 million people with diabetes; at this time, the estimated annual savings would be $15 million. This study provides a strong economic rationale for using deep learning systems as an assistive tool to screen for diabetic retinopathy. Ministry of Health, Singapore.

31 July 2019 in Current Diabetes Reports
Verified
Journal Article
Closed access
VBValentina Bellemo
Valentina Bellemo
GLGilbert Lim
Gilbert Lim
TRTyler Hyungtaek Rim
Tyler Hyungtaek Rim
GTGavin S. W. Tan
Gavin S. W. Tan
CCCarol Y. Cheung
Carol Y. Cheung
DTDarren Shu Jeng Ting
Darren Shu Jeng Ting

1 May 2013 in Investigative Ophthalmology & Visual Science
Verified
Journal Article
Open access
PDF file
ETEmanuele Trucco
Emanuele Trucco
ARAlfredo Ruggeri
Alfredo Ruggeri
TKThomas Karnowski
Thomas Karnowski
Luca GiancardoLuca Giancardo
Luca Giancardo
ECEdward Chaum
Edward Chaum
BDBal Dhillon
Bal Dhillon
This paper concerns the validation of automatic retinal image analysis (ARIA) algorithms. For reasons of space and consistency, we concentrate on the validation of algorithms processing color fundus camera images, currently the largest section of the ARIA literature. We sketch the context (imaging instruments and target tasks) of ARIA validation, summarizing the main image analysis and validation techniques. We then present a list of recommendations focusing on the creation of large repositories of test data created by international consortia, easily accessible via moderated Web sites, including multicenter annotations by multiple experts, specific to clinical tasks, and capable of running submitted software automatically on the data stored, with clear and widely agreed-on performance criteria, to provide a fair comparison.