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Article type: Short Communication
Authors: Thunell, Johannaa | Ferido, Patriciaa | Zissimopoulos, Juliea; b; *
Affiliations: [a] USC Schaeffer Center for Health Policy and Economics, Los Angeles, CA, USA | [b] USC Price School of Public Policy, Los Angeles, CA, USA
Correspondence: [*] Correspondence to: Julie Zissimopoulos, PhD, USC Price School of Public Policy, Schaeffer Center for Health Policy and Economics, University of Southern California, 635 Downey Way, Los Angeles, CA 90089, USA. Tel.: +1 213 821 7947; E-mail: zissimop@usc.edu.
Abstract: We examined how methods used for identifying dementia in administrative claims affected dementia incidence across racial/ethnic populations using a 100% sample of Medicare beneficiaries (n = 23,793,452). We found levels differed by method from 3.1% annual incidence to 3.6% in 2014. Dementia incidence declined from 2007 to 2014, but choice of method differentially impacted levels and trends by race/ethnicity. Methods using codes for dementia diagnosis and drugs to treat symptoms identified proportionally more Hispanics and Asians with dementia than other race/ethnicities, while codes for dementia diagnosis, drugs, and symptoms identified proportionally more whites and American Indians/Alaska Natives with dementia than other race/ethnicities.
Keywords: Alzheimer’s disease, dementia, diagnosis, incidence, measurement
DOI: 10.3233/JAD-190310
Journal: Journal of Alzheimer's Disease, vol. 72, no. 1, pp. 29-33, 2019
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