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. Author manuscript; available in PMC: 2021 Jan 23.
Published in final edited form as: J Alzheimers Dis. 2020;76(2):579–589. doi: 10.3233/JAD-200133

Table 1.

Sample description of individuals with use of an antidementia drug, or a diagnosis of AD, non-AD dementia, or dementia-related symptoms (2008–2016)

N 721,878
Patient Characteristics
 Female (N, %) 477,641 (66.2%)
 Age at index date (mean, SD) 80.40 (7.77)
 White (N, %) 600,358 (83.2%)
 Black (N, %) 57,412 (8.0%)
 Hispanic (N, %) 44,082(6.1%)
 Asian (N, %) 20,026 (2.8%)
 Dual eligible (N, %) 225,783 (31.3%)
 Low income subsidy (N, %) 35,593 (4.9%)
 Physician visits in year of index date (mean, SD) 10.09 (8.95)
 HCC (mean, SD) 1.90(1.47)
 Ever saw a specialist (N, %) 255,213 (36.5%)
Dementia-related diagnoses (N, %)
 Alzheimer’s disease 197,561 (27.4%)
 Non-AD dementia 514,633 (71.3%)
 Dementia-related symptoms 420,987 (58.3%)
 Used antidementia drug without diagnosis 11,558 (1.6%)
Antidementia drug use (N, %)
 Any AChEI 208,731 (28.9%)
 Any AChEI & Memantine 70,880 (9.8%)
 Donepezil 187,076 (25.9%)
 Galantamine 6,059 (0.8%)
 Memantine 99,556 (13.8%)
 Rivastigmine 42,484 (5.9%)
Comorbidities, ever diagnosed (N, %)
 Chronic obstructive pulmonary disease 341,695 (47.3%)
 Asthma 166,987 (23.1%)
 Chronic kidney disease 407,612 (56.5%)
 Hypertension 686,880 (95.2%)
 Heart failure 422,864 (58.6%)
 Glaucoma 229,025 (31.7%)
 Acute myocardial infarction 90,192(12.5%)
 Atrial fibrillation 246,688 (34.2%)
 Ischemic heart disease 535,606 (74.2%)

2008–2016 Medicare claims data (20% sample) for individuals aged 67+, with 3 consecutive years of enrollment in fee-for-service and Part D. Drug use defined as at least 7 days and 1 claim for any of the 4 AD drugs [3 AChEIs (donepezil, galantamine, rivastigmine) and memantine]. Index date is first diagnosis, or first antidementia drug use. AD, Alzheimer’s disease; AChEI, acetylcholinesterase inhibitor; ADRD, AD and related dementias; HCC, hierarchical condition category; dx, diagnosis. Dementia-related symptoms are amnesia, aphasia, other symbolic dysfunctions, apraxia, agnosia, and mild cognitive impairment.