| Literature DB >> 35600754 |
Sina Nawzad1, Wiepke Cahn2, Heshu Abdullah-Koolmees3.
Abstract
Patients with dementia often suffer from behavioral changes. A common behavioral change is acute physical aggressive behavior which is the most distressing change. This can lead to harm, which is especially problematic in nursing homes. Despite the serious safety concerns, antipsychotics are often prescribed to combat this problem. This article is aimed to review the evidence of the efficacy of utilizing antipsychotics in acutely treating physical aggressive behavior in patients with dementia in nursing homes. Therefore, a systematic literature search was performed. The results demonstrated that a meta-analysis confirmed statistically significant reduction in physical aggression when risperidone was compared to placebo. However, a randomized controlled trial showed no change in physical aggressive behavior between quetiapine and placebo. More research is needed to fully investigate the benefits of physical aggressive behavior and safety concerns of all the antipsychotics in patients with dementia in nursing homes.Entities:
Keywords: Cohen-Mansfield Agitation Inventory (CMAI) scale; aggressive behavior; antipsychotics; dementia; neuropsychiatric symptoms
Year: 2022 PMID: 35600754 PMCID: PMC9118396 DOI: 10.1177/20451253221097452
Source DB: PubMed Journal: Ther Adv Psychopharmacol ISSN: 2045-1253
Summary of trial design.[12–16]
| Study | Objective | Patient selection | Trial design | Efficacy assessment |
|---|---|---|---|---|
| Meta-analysis De Deyn | Pooled data analysis that examined the efficacy of risperidone for the treatment of aggression associated with dementia in elderly nursing home residents. | Patients (aged > 55 years) lived in an institution and had to have been diagnosed according to | 12-week, phase IIIA, double-blind, placebo-controlled, parallel-group preceded by 1-week single-blind washout periods during which all other psychotropic medications were discontinued. | Change in CMAI physical-aggression score from baseline to evaluated points (weeks 4, 8, 12, and at endpoint). |
| Zhong | To evaluate the efficacy of two fixed doses of quetiapine compared with placebo in treating agitation in patients with dementia. | Patients (aged > 55 years) were residents of nursing homes and assisted living facilities. They had diagnoses of probable or possible AD or vascular dementia according to | 10-week, randomized, multicenter, double-blind, placebo-controlled, fixed-dose (quetiapine 200 and 100 mg/day) study. | Change in CMAI physical-aggression score from baseline to evaluated points (weeks 1, 2, 4, 6, and 10 or at study withdrawal) |
AD: Alzheimer’s disease; BPSD: behavioral and psychological symptoms of dementia; CMAI: Cohen-Mansfield agitation inventory; DSM-IV: Diagnostic and Statistical Manual of Mental Disorders–Fourth Edition; NINCDS/ADRDA: National Institute of Neurological and Communicative Disorders and Stroke/the Alzheimer’s Disease and Related Disorders Association.
Results of the CMAI physical-aggression subscale score: mean change from baseline to endpoint.[12,16].
| Intervention | Placebo | Overall | ||||||
|---|---|---|---|---|---|---|---|---|
| Study | Intervention, mean dose (mg/day) |
| 95% CI |
|
| 95% CI | ||
| De Deyn | Risperidone, 1.0 | 713 | −3.5 (0.34) | −4.21; −2.87 | 426 | −1.4 (0.48) | −2.32; −3.2 | <0.001 |
| Zhong | Quetiapine, 100 | 120 | −3.2 (0.9) | −1.7; 2.2 | 94 | −2.9 (0.8) | Missing data | 0.796 |
| Quetiapine, 200 | 114 | −3.7 (0.9) | −2.0; 1.9 | 0.976 | ||||
CI: confidence Interval; CMAI: Cohen–Mansfield agitation inventory; SE, standard error.