Diagnosing Early Onset Dementia and Then What? A Frustrating System of Aftercare Resources

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Diagnosing Early Onset Dementia and Then What? A Frustrating System of Aftercare Resources

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Title: Diagnosing Early Onset Dementia and Then What? A Frustrating System of Aftercare Resources
Author: Schamber, S; Tarbi, EC; Avila-Urizar, M; Chemali, Zeina N.; Acar, Diler

Note: Order does not necessarily reflect citation order of authors.

Citation: Chemali, Z., S. Schamber, E.C. Tarbi, D. Acar, and M. Avila-Urizar. 2012. Diagnosing early onset dementia and then what? A frustrating system of aftercare resources. International Journal of General Medicine 2012(5): 81-86.
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Abstract: Recent studies indicate that the prevalence of early onset dementia (EOD) is more common than it was once presumed. As such, and considering the substantial challenges EOD presents to the patient, caregivers, and health care providers, this study sought to investigate the mechanism of care delivered to these patients. A medical record chart review was conducted for 85 patients attending a memory disorder unit who initially presented to rule out EOD as a working diagnosis. The results suggest that while the majority of these patients received an extensive work-up and were heavily medicated, they remained at home, where they lacked adequate age-related services and could not be placed, despite the crippling caregiver burden. This manuscript is a platform to discuss our current system limitations in the care of these patients with an eye on new opportunities for this challenging group.
Published Version: doi:10.2147/IJGM.S26523
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265995/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10288954
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