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Randomized Controlled Trial
. 2009 Sep;17(9):744-51.
doi: 10.1097/JGP.0b013e3181ab8c61.

Prazosin for the treatment of behavioral symptoms in patients with Alzheimer disease with agitation and aggression

Affiliations
Randomized Controlled Trial

Prazosin for the treatment of behavioral symptoms in patients with Alzheimer disease with agitation and aggression

Lucy Y Wang et al. Am J Geriatr Psychiatry. 2009 Sep.

Abstract

Objectives: Agitation/aggression in Alzheimer disease (AD) is a major cause of patient distress, caregiver burden, and institutionalization. Enhanced behavioral responsiveness to central nervous system norepinephrine (NE) release may contribute to the pathophysiology of agitation/aggression in AD. Prazosin, a nonsedating generic medication used for hypertension and benign prostatic hypertrophy, antagonizes NE effects at brain postsynaptic alpha-1 adrenoreceptors. This pilot study examined the efficacy and tolerability of prazosin for behavioral symptoms in patients with agitation/aggression in AD.

Design: Double-blind, placebo controlled, parallel group study.

Setting: A university AD center and a nursing home in Seattle, WA.

Participants: Twenty-two nursing home and community-dwelling participants with agitation/aggression and probable or possible AD (mean age: 80.6 +/- 11.2).

Intervention: Randomization to placebo (N = 11) or prazosin (N = 11). Medication was initiated at 1 mg/day and increased up to 6 mg/day using a flexible dosing algorithm.

Measurements: The Brief Psychiatric Rating Scale (BPRS) and Neuropsychiatric Inventory (NPI) at Weeks 1, 2, 4, 6, and 8. The Clinical Global Impression of Change (CGIC) at Week 8.

Results: Participants taking prazosin (mean dose: 5.7 +/- 0.9 mg/day) had greater improvements than those taking placebo (mean dose: 5.6 +/- 1.2 mg/day) on the NPI (mean change: -19 +/- 21 versus -2 +/- 15, chi = 6.32, df = 1, p = 0.012) and BPRS (mean change: -9 +/- 9 versus -3 +/- 5, chi = 4.42, df = 1, p = 0.036) based on linear mixed effects models and the CGIC (mean: 2.6 +/- 1.0 versus 4.5 +/- 1.6, z = 2.57, p = 0.011 [Mann-Whitney test]). Adverse effects and blood pressure changes were similar between prazosin and placebo groups.

Conclusion: Prazosin was well tolerated and improved behavioral symptoms in patients with agitation/aggression in AD.

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References

    1. Cohen-Mansfield J, Marx MS, Rosenthal AS. A description of agitation in a nursing home. J Gerontol. 1989;44:M77–84. - PubMed
    1. Selbaek G, Kirkevold O, Engedal K. The course of psychiatric and behavioral symptoms and the use of psychotropic medication in patients with dementia in Norwegian nursing homes--a 12-month follow-up study. Am J Geriatr Psychiatry. 2008;16:528–536. - PubMed
    1. Swearer JM, Drachman DA, O’Donnell BF, et al. Troublesome and disruptive behaviors in dementia. Relationships to diagnosis and disease severity. J Am Geriatr Soc. 1988;36:784–790. - PubMed
    1. Borson S, Liptzin B, Nininger J, et al. Psychiatry and the nursing home. Am J Psychiatry. 1987;144:1412–1418. - PubMed
    1. Rabins PV, Mace NL, Lucas MJ. The impact of dementia on the family. JAMA. 1982;248:333–335. - PubMed

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