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Merck

Galantamine versus risperidone for agitation in people with dementia: a randomized, twelve-week, single-center study.

Dementia and geriatric cognitive disorders (2014-06-28)
Yvonne Freund-Levi, Victor Bloniecki, Bjørn Auestad, Ann Christine Tysen Bäckström, Marie Lärksäter, Dag Aarsland
RESUMEN

To examine the effects of galantamine and risperidone on agitation in patients with dementia. A total of 100 patients with dementia and neuropsychiatric symptoms (mean age ± SD: 78.6 ± 7.5 years; 67% female) were included in this 12-week, randomized, parallel-group, controlled, single-center trial. The participants received galantamine (n = 50; target dose: 24 mg) or risperidone (n = 50; target dose: 1.5 mg) for 12 weeks. Both galantamine and risperidone treatment resulted in reduced agitation. However, risperidone showed a significant advantage over galantamine both at week 3 (mean difference in total Cohen-Mansfield Agitation Inventory score: 3.7 points; p = 0.03) and at week 12 (4.3 points; p = 0.01). Agitation improved in both groups, even if the treatment effects were more pronounced in the risperidone group; however, the effects on cognition and other aspects of tolerability were stronger with galantamine.

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Sigma-Aldrich
Risperidone, ≥98% (HPLC), powder
USP
Risperidone, United States Pharmacopeia (USP) Reference Standard
Risperidone for system suitability, European Pharmacopoeia (EP) Reference Standard
Risperidone, European Pharmacopoeia (EP) Reference Standard