Antony Sutherland, Christopher Kyndt, David Darby, Maja Christensen, Fari Islam, Samantha M Loi, Amy Brodtmann
{"title":"2009-2019年澳大利亚三级认知神经病学门诊转诊模式和诊断结果","authors":"Antony Sutherland, Christopher Kyndt, David Darby, Maja Christensen, Fari Islam, Samantha M Loi, Amy Brodtmann","doi":"10.1002/dad2.70120","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Young-onset dementia (YOD) and atypical dementias often experience diagnostic delays, particularly in outpatient settings where timely referrals are crucial.</p><p><strong>Methods: </strong>A 10-year retrospective audit (2009-2019) of 626 patients at a specialist cognitive neurology clinic reviewed demographics, referral sources, and time to diagnosis. Data were compared between YOD and late-onset dementia (LOD), and with and without dementia groups.</p><p><strong>Results: </strong>Fifty-three percent of patients were diagnosed with dementia (mean age: 65 ± 11.9 years). Non-neurodegenerative conditions were more frequent in < 65 years (61%). Among YOD cases, Alzheimer's dementia (AD) and behavioral variant frontotemporal dementia accounted for 40% and 34% of diagnoses, respectively, while AD predominated in LOD (65%). Language-variant dementias were similar between groups (14%). Diagnostic delays in YOD averaged 1 year longer than in LOD.</p><p><strong>Discussion: </strong>Higher YOD and language-variant dementia referrals to specialist services reveal diagnostic delays, underscoring the need for better referral and diagnostic pathways.</p><p><strong>Highlights: </strong>Delayed diagnosis common in young-onset dementia (YOD) and atypical dementia.Specialist clinics see more YOD and language-variant dementia referrals.YOD has longer time from symptom onset to diagnosis compared to late-onset cases.Behavioral variant frontotemporal dementia (bvFTD) a more common diagnosis in YOD patients.</p>","PeriodicalId":53226,"journal":{"name":"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring","volume":"17 2","pages":"e70120"},"PeriodicalIF":4.0000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12122257/pdf/","citationCount":"0","resultStr":"{\"title\":\"Referral patterns and diagnostic outcomes in an outpatient Australian tertiary cognitive neurology service: 2009-2019.\",\"authors\":\"Antony Sutherland, Christopher Kyndt, David Darby, Maja Christensen, Fari Islam, Samantha M Loi, Amy Brodtmann\",\"doi\":\"10.1002/dad2.70120\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Young-onset dementia (YOD) and atypical dementias often experience diagnostic delays, particularly in outpatient settings where timely referrals are crucial.</p><p><strong>Methods: </strong>A 10-year retrospective audit (2009-2019) of 626 patients at a specialist cognitive neurology clinic reviewed demographics, referral sources, and time to diagnosis. Data were compared between YOD and late-onset dementia (LOD), and with and without dementia groups.</p><p><strong>Results: </strong>Fifty-three percent of patients were diagnosed with dementia (mean age: 65 ± 11.9 years). Non-neurodegenerative conditions were more frequent in < 65 years (61%). Among YOD cases, Alzheimer's dementia (AD) and behavioral variant frontotemporal dementia accounted for 40% and 34% of diagnoses, respectively, while AD predominated in LOD (65%). Language-variant dementias were similar between groups (14%). Diagnostic delays in YOD averaged 1 year longer than in LOD.</p><p><strong>Discussion: </strong>Higher YOD and language-variant dementia referrals to specialist services reveal diagnostic delays, underscoring the need for better referral and diagnostic pathways.</p><p><strong>Highlights: </strong>Delayed diagnosis common in young-onset dementia (YOD) and atypical dementia.Specialist clinics see more YOD and language-variant dementia referrals.YOD has longer time from symptom onset to diagnosis compared to late-onset cases.Behavioral variant frontotemporal dementia (bvFTD) a more common diagnosis in YOD patients.</p>\",\"PeriodicalId\":53226,\"journal\":{\"name\":\"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring\",\"volume\":\"17 2\",\"pages\":\"e70120\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-05-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12122257/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/dad2.70120\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/4/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/dad2.70120","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Referral patterns and diagnostic outcomes in an outpatient Australian tertiary cognitive neurology service: 2009-2019.
Introduction: Young-onset dementia (YOD) and atypical dementias often experience diagnostic delays, particularly in outpatient settings where timely referrals are crucial.
Methods: A 10-year retrospective audit (2009-2019) of 626 patients at a specialist cognitive neurology clinic reviewed demographics, referral sources, and time to diagnosis. Data were compared between YOD and late-onset dementia (LOD), and with and without dementia groups.
Results: Fifty-three percent of patients were diagnosed with dementia (mean age: 65 ± 11.9 years). Non-neurodegenerative conditions were more frequent in < 65 years (61%). Among YOD cases, Alzheimer's dementia (AD) and behavioral variant frontotemporal dementia accounted for 40% and 34% of diagnoses, respectively, while AD predominated in LOD (65%). Language-variant dementias were similar between groups (14%). Diagnostic delays in YOD averaged 1 year longer than in LOD.
Discussion: Higher YOD and language-variant dementia referrals to specialist services reveal diagnostic delays, underscoring the need for better referral and diagnostic pathways.
Highlights: Delayed diagnosis common in young-onset dementia (YOD) and atypical dementia.Specialist clinics see more YOD and language-variant dementia referrals.YOD has longer time from symptom onset to diagnosis compared to late-onset cases.Behavioral variant frontotemporal dementia (bvFTD) a more common diagnosis in YOD patients.
期刊介绍:
Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.