Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/114201
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dc.contributorSchool of Optometryen_US
dc.creatorLian, Jen_US
dc.creatorSo, Cen_US
dc.creatorMcGhee, SMen_US
dc.creatorThach, TQen_US
dc.creatorLam, CLKen_US
dc.creatorFung, CSCen_US
dc.creatorKwong, ASKen_US
dc.creatorChan, JCHen_US
dc.date.accessioned2025-07-15T08:44:20Z-
dc.date.available2025-07-15T08:44:20Z-
dc.identifier.issn2233-6079en_US
dc.identifier.urihttp://hdl.handle.net/10397/114201-
dc.language.isoenen_US
dc.publisherKorean Diabetes Association,Daehan Dangnyobyeong Hakoeen_US
dc.rightsCopyright © 2025 Korean Diabetes Associationen_US
dc.rightsT his is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication Lian J, So C, McGhee SM, Thach T, Lam CLK, Fung CSC, et al. To Determine the Risk-Based Screening Interval for Diabetic Retinopathy: Development and Validation of Risk Algorithm from a Retrospective Cohort Study. Diabetes Metab J 2025;49:286-297 is available at https://doi.org/10.4093/dmj.2024.0142.en_US
dc.subjectCohort studiesen_US
dc.subjectDiabetic retinopathyen_US
dc.subjectPrognosisen_US
dc.subjectTime-to-treatmenten_US
dc.subjectVision screeningen_US
dc.titleTo determine the risk-based screening interval for diabetic retinopathy : development and validation of risk algorithm from a retrospective cohort studyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage286en_US
dc.identifier.epage297en_US
dc.identifier.volume49en_US
dc.identifier.issue2en_US
dc.identifier.doi10.4093/dmj.2024.0142en_US
dcterms.abstractBackground: The optimal screening interval for diabetic retinopathy (DR) remains controversial. This study aimed to develop a risk algorithm to predict the individual risk of referable sight-threatening diabetic retinopathy (STDR) in a mainly Chinese population and to provide evidence for risk-based screening intervals.en_US
dcterms.abstractMethods: The retrospective cohort data from 117,418 subjects who received systematic DR screening in Hong Kong between 2010 and 2016 were included to develop and validate the risk algorithm using a parametric survival model. The risk algorithm can be used to predict the individual risk of STDR within a specific time interval, or the time to reach a specific risk margin and thus to allocate a screening interval. The calibration performance was assessed by comparing the cumulative STDR events versus predicted risk over 2 years, and discrimination by using receiver operative characteristics (ROC) curve.en_US
dcterms.abstractResults: Duration of diabetes, glycosylated hemoglobin, systolic blood pressure, presence of chronic kidney disease, diabetes medication, and age were included in the risk algorithm. The validation of prediction performance showed that there was no significant difference between predicted and observed STDR risks in males (5.6% vs. 5.1%, P=0.724) or females (4.8% vs. 4.6%, P=0.099). The area under the receiver operating characteristic curve was 0.80 (95% confidence interval [CI], 0.78 to 0.81) for males and 0.81 (95% CI, 0.79 to 0.83) for females.en_US
dcterms.abstractConclusion: The risk algorithm has good prediction performance for referable STDR. Using a risk-based screening interval allows us to allocate screening visits disproportionally more to those at higher risk, while reducing the frequency of screening of lower risk people.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationDiabetes & metabolism journal, Mar. 2025, v. 49, no. 2, p. 286-297en_US
dcterms.isPartOfDiabetes & metabolism journalen_US
dcterms.issued2025-03-
dc.identifier.scopus2-s2.0-105000973766-
dc.identifier.eissn2233-6087en_US
dc.description.validate202507 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera3892-
dc.identifier.SubFormID51574-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextHMRFen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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