Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/88170
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dc.contributorDepartment of Applied Mathematicsen_US
dc.contributorSchool of Optometryen_US
dc.contributorSchool of Nursingen_US
dc.creatorYang, Len_US
dc.creatorChu, TKen_US
dc.creatorLian, JXen_US
dc.creatorLo, CWen_US
dc.creatorZhao, Sen_US
dc.creatorHe, DHen_US
dc.creatorQin, Jen_US
dc.creatorLiang, Jen_US
dc.date.accessioned2020-09-18T02:13:23Z-
dc.date.available2020-09-18T02:13:23Z-
dc.identifier.urihttp://hdl.handle.net/10397/88170-
dc.language.isoenen_US
dc.publisherBMJ Publishing Group Ltden_US
dc.rightsThis is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.en_US
dc.rights© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.en_US
dc.rightsThe following publication Yang, L., Chu, T. K., Lian, J. X., Lo, C. W., Zhao, S., He, D. H., . . . Liang, J. (2020). Individualised risk prediction model for new-onset, progression and regression of chronic kidney disease in a retrospective cohort of patients with type 2 diabetes under primary care in Hong Kong. Bmj Open, 10(7), 1-9 is available at https://dx.doi.org/10.1136/bmjopen-2019-035308en_US
dc.subjectDiabetic nephropathy & vascular diseaseen_US
dc.subjectEpidemiologyen_US
dc.subjectPrimary careen_US
dc.subjectStatistics & research methodsen_US
dc.titleIndividualised risk prediction model for new-onset, progression and regression of chronic kidney disease in a retrospective cohort of patients with type 2 diabetes under primary care in Hong Kongen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1en_US
dc.identifier.epage9en_US
dc.identifier.volume10en_US
dc.identifier.issue7en_US
dc.identifier.doi10.1136/bmjopen-2019-035308en_US
dcterms.abstractObjectives This study is aimed to develop and validate a prediction model for multistate transitions across different stages of chronic kidney disease (CKD) in patients with type 2 diabetes mellitus under primary care. Setting We retrieved the anonymised electronic health records of a population-based retrospective cohort in Hong Kong. Participants A total of 26 197 patients were included in the analysis. Primary and secondary outcome measures The new-onset, progression and regression of CKD were defined by the transitions of four stages that were classified by combining glomerular filtration rate and urine albumin-to-creatinine ratio. We applied a multiscale multistate Poisson regression model to estimate the rates of the stage transitions by integrating the baseline demographic characteristics, routine laboratory test results and clinical data from electronic health records.en_US
dcterms.abstractResults During the mean follow-up time of 1.8 years, there were 2632 patients newly diagnosed with CKD, 1746 progressed to the next stage and 1971 regressed into an earlier stage. The models achieved the best performance in predicting the new-onset and progression with the predictors of sex, age, body mass index, systolic blood pressure, diastolic blood pressure, serum creatinine, haemoglobin A1c, total cholesterol, low-density lipoprotein, high-density lipoprotein, triglycerides and drug prescriptions.en_US
dcterms.abstractConclusions This study demonstrated that individual risks of new-onset and progression of CKD can be predicted from the routine physical and laboratory test results. The individualised prediction curves developed from this study could potentially be applied to routine clinical practices, to facilitate clinical decision making, risk communications with patients and early interventions.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBMJ open, July 2020, v. 10, no. 7, e035308, p. 1-9en_US
dcterms.isPartOfBMJ openen_US
dcterms.issued2020-07-
dc.identifier.isiWOS:000561427800058-
dc.identifier.pmid32641324-
dc.identifier.eissn2044-6055en_US
dc.identifier.artne035308en_US
dc.description.validate202009 bcrcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera0982-n22, OA_Scopus/WOSen_US
dc.identifier.SubFormID2281-
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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