Please use this identifier to cite or link to this item: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12959
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dc.contributor.authorTeasdale, S. B.-
dc.contributor.authorArdill-Young, O.-
dc.contributor.authorMorell, R.-
dc.contributor.authorWard, P. B.-
dc.contributor.authorKhandaker, G. M.-
dc.contributor.authorUpthegrove, R.-
dc.contributor.authorCurtis, J.-
dc.contributor.authorPerry, B. I.-
dc.date.accessioned2024-09-02T05:56:58Z-
dc.date.available2024-09-02T05:56:58Z-
dc.date.issued2024-
dc.identifier.issn10398562 (ISSN)-
dc.identifier.urihttps://swslhd.intersearch.com.au/swslhdjspui/handle/1/12959-
dc.description.abstractObjective: To examine the accuracy and likely clinical usefulness of the Psychosis Metabolic Risk Calculator (PsyMetRiC) in predicting up-to six-year risk of incident metabolic syndrome in an Australian sample of young people with first-episode psychosis. Method: We conducted a retrospective study at a secondary care early psychosis treatment service among people aged 16-35 years, extracting relevant data at the time of antipsychotic commencement and between one-to-six-years later. We assessed algorithm accuracy primarily via discrimination (C-statistic), calibration (calibration plots) and clinical usefulness (decision curve analysis). Model updating and recalibration generated a site-specific (Australian) PsyMetRiC version. Results: We included 116 people with baseline and follow-up data: 73% male, mean age 20.1 years, mean follow-up 2.6 years, metabolic syndrome prevalence 13%. C-statistics for both partial- (C = 0.71, 95% CI 0.64-0.75) and full-models (C = 0.72, 95% CI 0.65-0.77) were acceptable; however, calibration plots demonstrated consistent under-prediction of risk. Recalibration and updating led to slightly improved C-statistics, greatly improved agreement between observed and predicted risk, and a narrow window of likely clinical usefulness improved significantly. Conclusion: An updated and recalibrated PsyMetRiC model, PsyMetRiC-Australia, shows promise. Validation in a large sample is required to confirm its accuracy and clinical usefulness for the Australian population. � The Royal Australian and New Zealand College of Psychiatrists 2024.-
dc.publisherSAGE Publications Inc.-
dc.subjectantipsychotic mental disorders metabolic syndrome psychosis risk prediction validation study-
dc.titleMetabolic syndrome risk prediction in an Australian sample with first-episode psychosis using the psychosis metabolic risk calculator: A validation study-
dc.typeJournal Article-
dc.contributor.swslhdauthorWard, Philip B.-
dc.description.affiliatesDiscipline of Psychiatry and Mental Health, School of Clinical Medicine, UNSW Sydney, Kensington, NSW, Australia Mindgardens Neuroscience Network, Randwick, NSW, Australia Schizophrenia Research Unit, South Western Sydney Local Health District, Ingham Institute of Applied Medical Research, Liverpool Hospital, Liverpool, NSW, Australia Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom Centre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom Institute for Mental Health and Centre for Human Brain Health, University of Birmingham, Birmingham, United Kingdom Early Intervention Service, Birmingham Women?s and Children?s NHS Foundation Trust, Birmingham, United Kingdom Early Psychosis Programme, South Eastern Sydney Local Health District, Bondi Junction, NSW, Australia Department of General Psychiatry, Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, United Kingdom-
dc.identifier.doi10.1177/10398562241269171-
dc.identifier.departmentLiverpool Hospital, Schizophrenia Research Unit-
dc.type.studyortrialArticle-
dc.identifier.journaltitleAustralasian Psychiatry-
Appears in Collections:Liverpool Hospital
South Western Sydney Local Health District

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