Pharmaceutical Treatment for Alzheimer's Disease and Related Dementias: Utilization and Disparities.


Journal

Journal of Alzheimer's disease : JAD
ISSN: 1875-8908
Titre abrégé: J Alzheimers Dis
Pays: Netherlands
ID NLM: 9814863

Informations de publication

Date de publication:
2020
Historique:
pubmed: 17 6 2020
medline: 8 5 2021
entrez: 16 6 2020
Statut: ppublish

Résumé

Four prescription drugs (donepezil, galantamine, memantine, and rivastigmine) are approved by the US FDA to treat symptoms of Alzheimer's disease (AD). Even modest effectiveness could potentially reduce the population-level burden of AD and related dementias (ADRD), especially for women and racial/ethnic minorities who have higher incidence of ADRD. Describe the prevalence of antidementia drug use and timing of initiation relative to ADRD diagnosis among a nationally representative group of older Americans, and if there are disparities in prevalence and timing by sex and race/ethnicity. Descriptive analyses and logistic regressions of Medicare claims (2008-2016) for beneficiaries who had an ADRD or dementia-related symptom diagnosis, or use of an FDA approved drug for AD. We investigate prevalence of use and timing of treatment initiation relative to ADRD diagnosis across time and beneficiary characteristics (age, sex, race/ethnicity, socioeconomic status, comorbidities). Among persons diagnosed with ADRD or related symptoms, 33.3% used an approved drug over the study period. Odds of use was higher among Whites than non-Whites. Among ADRD drug users, 40% initiated use within 6 months of the initial ADRD or related symptoms diagnosis, and 16% initiated prior to a diagnosis. We observed disparities by race/ethnicity: 28% of Asians, 24% of Hispanics, 16% of Blacks, and 15% of Whites initiated prior to diagnosis. The use of antidementia drugs is relatively low and varies widely by race/ethnicity. Heterogeneity in timing of initiation and use may affect health and cost outcomes, but these effects merit further study.

Sections du résumé

BACKGROUND
Four prescription drugs (donepezil, galantamine, memantine, and rivastigmine) are approved by the US FDA to treat symptoms of Alzheimer's disease (AD). Even modest effectiveness could potentially reduce the population-level burden of AD and related dementias (ADRD), especially for women and racial/ethnic minorities who have higher incidence of ADRD.
OBJECTIVE
Describe the prevalence of antidementia drug use and timing of initiation relative to ADRD diagnosis among a nationally representative group of older Americans, and if there are disparities in prevalence and timing by sex and race/ethnicity.
METHODS
Descriptive analyses and logistic regressions of Medicare claims (2008-2016) for beneficiaries who had an ADRD or dementia-related symptom diagnosis, or use of an FDA approved drug for AD. We investigate prevalence of use and timing of treatment initiation relative to ADRD diagnosis across time and beneficiary characteristics (age, sex, race/ethnicity, socioeconomic status, comorbidities).
RESULTS
Among persons diagnosed with ADRD or related symptoms, 33.3% used an approved drug over the study period. Odds of use was higher among Whites than non-Whites. Among ADRD drug users, 40% initiated use within 6 months of the initial ADRD or related symptoms diagnosis, and 16% initiated prior to a diagnosis. We observed disparities by race/ethnicity: 28% of Asians, 24% of Hispanics, 16% of Blacks, and 15% of Whites initiated prior to diagnosis.
CONCLUSIONS
The use of antidementia drugs is relatively low and varies widely by race/ethnicity. Heterogeneity in timing of initiation and use may affect health and cost outcomes, but these effects merit further study.

Identifiants

pubmed: 32538845
pii: JAD200133
doi: 10.3233/JAD-200133
pmc: PMC7825250
mid: NIHMS1662157
doi:

Substances chimiques

Cholinesterase Inhibitors 0
Dopamine Agents 0
Nootropic Agents 0
Galantamine 0D3Q044KCA
Donepezil 8SSC91326P
Rivastigmine PKI06M3IW0
Memantine W8O17SJF3T

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

579-589

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL126804
Pays : United States
Organisme : ACL HHS
ID : U01CE002967
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL130462
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG033559
Pays : United States
Organisme : NIA NIH HHS
ID : R34 AG049652
Pays : United States
Organisme : NIA NIH HHS
ID : K76 AG059929
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG055401
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG006781
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG043073
Pays : United States

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Auteurs

Douglas Barthold (D)

The Comparative Health Outcomes, Policy, and Economics (CHOICE) Institute, Department of Pharmacy, University of Washington, Seattle, WA, USA.

Geoffrey Joyce (G)

School of Pharmacy, Schaeffer Center for Health Policy and Economics, University of Southern California, Los Angeles, CA, USA.

Patricia Ferido (P)

Price School of Public Policy, Schaeffer Center for Health Policy and Economics, University of Southern California, Los Angeles, CA, USA.

Emmanuel F Drabo (EF)

Health Policy and Management Department, Johns Hopkins University, Baltimore, MD, USA.

Zachary A Marcum (ZA)

The Comparative Health Outcomes, Policy, and Economics (CHOICE) Institute, Department of Pharmacy, University of Washington, Seattle, WA, USA.

Shelly L Gray (SL)

The Comparative Health Outcomes, Policy, and Economics (CHOICE) Institute, Department of Pharmacy, University of Washington, Seattle, WA, USA.

Julie Zissimopoulos (J)

Price School of Public Policy, Schaeffer Center for Health Policy and Economics, University of Southern California, Los Angeles, CA, USA.

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Classifications MeSH