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Health care in adults with Down syndrome: a longitudinal cohort study

dc.contributor.authorJensen, K. M.en_US
dc.contributor.authorDavis, M. M.en_US
dc.date.accessioned2013-09-04T17:18:30Z
dc.date.available2014-12-01T17:22:17Zen_US
dc.date.issued2013-10en_US
dc.identifier.citationJensen, K. M.; Davis, M. M. (2013). "Health care in adults with Down syndrome: a longitudinal cohort study." Journal of Intellectual Disability Research (10): 947-958.en_US
dc.identifier.issn0964-2633en_US
dc.identifier.issn1365-2788en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/99631
dc.description.abstractBackground  Individuals with Down syndrome increasingly survive into adulthood, yet little is known about their healthcare patterns as adults. Our study sought to characterise patterns of health care among adults with Down syndrome based on whether they had fully transitioned to adult‐oriented providers by their inception in this cohort. Methods  In this retrospective observational cohort study, healthcare utilisation and annualised patient charges were evaluated in patients with Down syndrome aged 18–45 years who received care in a single academic health centre from 2000 to 2008. Comparisons were made based on patients' provider mix (only adult‐focused or ‘mixed’ child‐ and adult‐focused providers). Results  The cohort included 205 patients with median index age = 28 years; 52% of these adult patients had incompletely transitioned to adult providers and received components of their care from child‐focused providers. A higher proportion of these ‘mixed’ patients were seen exclusively by subspecialty providers (mixed = 81%, adult = 46%, P  < 0.001), suggesting a need for higher intensity specialised services. Patients in the mixed provider group incurred higher annualised charges in analyses adjusted for age, mortality, total annualised encounters, and number of subspecialty disciplines accessed. These differences were most pronounced when stratified by whether patients were hospitalised during the study period (e.g. difference in adjusted means between mixed versus adult provider groups: $571 without hospitalisation, $19 061 with hospitalisation). Conclusions  In this unique longitudinal cohort of over 200 adults aged 18–45 years with Down syndrome, over half demonstrated incomplete transition to adult care. Persistent use of child‐focused care, often with a subspecialty emphasis, has implications for healthcare charges. Future studies must identify reasons for distinct care patterns, examine their relationship with clinical outcomes, and evaluate which provider types deliver the highest quality care for adults with Down syndrome and a wide variety of comorbidities.en_US
dc.publisherBlackwell Publishing Ltden_US
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherHealthcare Utilisationen_US
dc.subject.otherHealth Services Researchen_US
dc.subject.otherIntellectual Disabilityen_US
dc.subject.otherHealthcare Transitionen_US
dc.subject.otherDown Syndromeen_US
dc.titleHealth care in adults with Down syndrome: a longitudinal cohort studyen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumGerald R. Ford School of Public Policy, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartments of Internal Medicine and Pediatrics, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/99631/1/jir1589.pdf
dc.identifier.doi10.1111/j.1365-2788.2012.01589.xen_US
dc.identifier.sourceJournal of Intellectual Disability Researchen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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