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Randomized Controlled Trial
. 2023 Nov;35(11):664-672.
doi: 10.1017/S1041610223000327. Epub 2023 Apr 17.

Cost consequence analysis of Apathy in Dementia Methylphenidate Trial 2 (ADMET 2)

Affiliations
Randomized Controlled Trial

Cost consequence analysis of Apathy in Dementia Methylphenidate Trial 2 (ADMET 2)

Krista L Lanctôt et al. Int Psychogeriatr. 2023 Nov.

Abstract

Background: This paper used data from the Apathy in Dementia Methylphenidate Trial 2 (NCT02346201) to conduct a planned cost consequence analysis to investigate whether treatment of apathy with methylphenidate is economically attractive.

Methods: A total of 167 patients with clinically significant apathy randomized to either methylphenidate or placebo were included. The Resource Utilization in Dementia Lite instrument assessed resource utilization for the past 30 days and the EuroQol five dimension five level questionnaire assessed health utility at baseline, 3 months, and 6 months. Resources were converted to costs using standard sources and reported in 2021 USD. A repeated measures analysis of variance compared change in costs and utility over time between the treatment and placebo groups. A binary logistic regression was used to assess cost predictors.

Results: Costs were not significantly different between groups whether the cost of methylphenidate was excluded (F(2,330) = 0.626, ηp2 = 0.004, p = 0.535) or included (F(2,330) = 0.629, ηp2 = 0.004, p = 0.534). Utility improved with methylphenidate treatment as there was a group by time interaction (F(2,330) = 7.525, ηp2 = 0.044, p < 0.001).

Discussion: Results from this study indicated that there was no evidence for a difference in resource utilization costs between methylphenidate and placebo treatment. However, utility improved significantly over the 6-month follow-up period. These results can aid in decision-making to improve quality of life in patients with Alzheimer's disease while considering the burden on the healthcare system.

Keywords: Alzheimer’s disease (AD); apathy; dementia; health economics.

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Conflict of interest statement

KLL has received research grants from the National Institutes of Aging, Alzheimer’s Drug Discovery Foundation, the Alzheimer Society of Canada, Alzheimer’s Association, Canadian Institutes of Health Research, Weston Brain Institute; honoraria from BioXcel, Cerevel, Eisai, and Praxis.

NH has received peer-reviewed research grants from the Alzheimer Drug Discovery Foundation, the Alzheimer Society of Canada, the National Institute of Health, Canadian Institutes of Health Research.

PBR has received research grants from the National Institutes of Aging, Alzheimer’s Clinical Trials Consortium, Richman Family Precision Medicine Center of Excellence on Alzheimer’s Disease, Eisai, Functional Neuromodulation, and Lilly; honoraria from GLG, Leerink, Cerevel, Cerevance, Bioxcel, Sunovion, Acadia, Medalink, Novo Nordisk, Noble Insights, TwoLabs, Otsuka, Lundbeck, Acadia, MedaCorp, ExpertConnect, HMP Global, Synaptogenix, and Neurology Week.

The remaining authors have nothing to disclose.

Comment in

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