Adherence and Tolerability of Alzheimer's Disease Medications: A Pragmatic Randomized Trial

Noll L Campbell, Anthony J Perkins, Sujuan Gao, Todd C Skaar, Lang Li, Hugh C Hendrie, Nicole Fowler, Christopher M Callahan, Malaz A Boustani, Noll L Campbell, Anthony J Perkins, Sujuan Gao, Todd C Skaar, Lang Li, Hugh C Hendrie, Nicole Fowler, Christopher M Callahan, Malaz A Boustani

Abstract

Background/objectives: Post-marketing comparative trials describe medication use patterns in diverse, real-world populations. Our objective was to determine if differences in rates of adherence and tolerability exist among new users to acetylcholinesterase inhibitors (AChEI's).

Design: Pragmatic randomized, open label comparative trial of AChEI's currently available in the United States.

Setting: Four memory care practices within four healthcare systems in the greater Indianapolis area.

Participants: Eligibility criteria included older adults with a diagnosis of possible or probable Alzheimer's disease (AD) who were initiating treatment with an AChEI. Participants were required to have a caregiver to complete assessments, access to a telephone, and be able to understand English. Exclusion criteria consisted of a prior severe adverse event from AChEIs.

Intervention: Participants were randomized to one of three AChEIs in a 1:1:1 ratio and followed for 18 weeks.

Measurements: Caregiver-reported adherence, defined as taking or not taking study medication, and caregiver-reported adverse events, defined as the presence of an adverse event.

Results: 196 participants were included with 74.0% female, 30.6% African Americans, and 72.9% who completed at least twelfth grade. Discontinuation rates after 18 weeks were 38.8% for donepezil, 53.0% for galantamine, and 58.7% for rivastigmine (P = .063) in the intent to treat analysis. Adverse events and cost explained 73.1% and 25.4% of discontinuation. No participants discontinued donepezil due to cost. Adverse events were reported by 81.2% of all participants; no between-group differences in total adverse events were statistically significant.

Conclusions: This pragmatic comparative trial showed high rates of adverse events and cost-related non-adherence with AChEIs. Interventions improving adherence and persistence to AChEIs may improve AD management.

Trial registration: Clinicaltrials.gov: NCT01362686 (https://ichgcp.net/clinical-trials-registry/NCT01362686).

Keywords: Alzheimer's; clinical care; dementia.

Conflict of interest statement

Conflict of Interest: The authors declare that they have no competing interests. Neither the funding agency nor any outside organization had a role in study design, data collection, data analysis, the decision to publish or manuscript preparation.

© 2017, Copyright the Authors Journal compilation © 2017, The American Geriatrics Society.

Figures

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Figure:
Description of participant flow through study procedures.

Source: PubMed

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