A double-blind randomised comparison of risperidone and haloperidol in the treatment of behavioural and psychological symptoms in Chinese dementia patients
✍ Scribed by Wai-chi Chan; Linda Chiu-wa Lam; Caroline Nga-pui Choy; Vivian Pui-yiu Leung; Siu-wah Li; Helen Fung-kum Chiu
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 76 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0885-6230
- DOI
- 10.1002/gps.504
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Background
Behavioural and psychological symptoms (BPSD) are common during the course of dementia and present severe problems to patients and their caregivers.
Objectives
To assess the therapeutic efficacy and safety of haloperidol and risperidone in treating BPSD in Chinese dementia patients.
Methods
A 12‐week double‐blind randomised comparison of haloperidol and risperidone treatments was conducted in 58 patients with DSM‐IV diagnosis of dementia of Alzheimer's type or vascular dementia. They were randomly assigned to receive flexible doses (0.5 to 2 mg/day) of haloperidol or risperidone. Clinical response was evaluated using the Cohen‐Mansfield Agitation Inventory (CMAI), the Behavioral Pathology in Alzheimer's Disease Rating Scale (BEHAVE‐AD), Simpson‐Angus Scale, Functional Assessment Staging and Cantonese version of the Mini‐Mental State Examination.
Results
The mean doses at the last week were 0.90 mg/day of haloperidol and 0.85 mg/day of risperidone. Both haloperidol and risperidone significantly reduced the severity of BPSD (scores on CMAI and BEHAVE‐AD), with no significant between‐group differences. Haloperidol‐treated patients showed a worsening on Simpson‐Angus scale while there was no significant change in this measure in risperidone‐treated patients.
Conclusions
Low‐dose haloperidol and risperidone were well tolerated and associated with reductions in the severity and frequency of behavioural symptoms in subjects with dementia. Risperidone may have a more favourable risk‐benefit profile in view of its lower propensity to induce extrapyramidal symptoms. Copyright © 2001 John Wiley & Sons, Ltd.
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