Takaisin Tulosta

Atypical antipsychotics for agitation and psychosis in people with Alzheimer’s disease and vascular dementia

Evidence summaries
3.3.2022 • Latest change 3.3.2022
Editors

Level of evidence: B

Atypical antipsychotics appear to have some effect on agitation in Alzheimer’s disease and vascular dementia.

The quality of evidence is downgraded by study limitations (incomplete outcome data, selective reporting and/or short follow-up).

Weak recommendation for using an intervention: ↑

Atypical antipsychotics are suggested for agitation in Alzheimer’s disease or vascular dementia, if nonpharmacological methods are insufficient.

The recommendation is weak because of uncertain trade-off between benefits and harms/burden of treatment.

Summary

A Cochrane review «Antipsychotics for agitation and psychosis in people with Alzheimer's disease and vascular dementia»1 «Mühlbauer V, Möhler R, Dichter MN et al. Antipsychotics for agitation and psychosis in people with Alzheimer's disease and vascular dementia. Cochrane Database Syst Rev 2021;(12):CD013304. »1 included 20 studies with a total of 5909 subjects. Neuropsychiatric symptoms are a common accompaniment of dementia. These include agitation/aggression, delusions and hallucinations. In some cases, the delusions or hallucinations meet the criteria for dementia-associated psychosis. Eight of the trials (n=2320) tested an atypical antipsychotic for agitation and 12 for psychosis (n=3589). The trials were performed in institutionalised or hospitalised for agitation and institutionalized, hospitalised and community-dwelling patients, or a combination of those, for psychosis. The trials had a duration between 3 to 12 weeks.

See table «Atypical antipsychotics compared to placebo in people with Alzheimer’s disease and vascular dementia.»1.

Table 1. Atypical antipsychotics compared to placebo in people with Alzheimer’s disease and vascular dementia.
OutcomesAbsolute mean change from baseline or absolute risk in each group Comparison of mean changes or risks between groups (treatment effect)
Placebo groupAntipsychotics group (95%CI) Relative effect, RR (95% CI) Absolute effect, MD or RD (95% CI)
Agitation in units on CMAI (higher is worse), baseline mean was 58.8; SMD 0.21 less (0.30 to 0.12) 15.0 decrease18.0 decrease (19.3 to 16.7)NA3.0 greater decrease (4.3 to 1.7)
Psychosis in units of NPI-NH P (higher is worse), baseline mean was 11.2; SMD 0.11 less (0.18 to 0.03) 4.7 decrease5.3 decrease (5.7 to 4.9) NA0.6 greater decrease (1.0 to 0.2)
Extrapyramidal symptoms8 per 10011 per 100 (9 to 14) 1.39 (1.14 to 1.68)3 more per 100 (1 to 6 more)
Somnolence7 per 10014 per 100 (11 to 17) 1.93 (1.57 to 2.39)7 more per 100 (4 to 10 more)
Death19 per 100026 per 1000 (17 to 39) 1.36 (0.90 to 2.05)7 more per 1000 (2 less to 20 more)

Clinical comments

Overall, the evidence shows that most of the decrease in agitation and psychosis seen can be attributed to a favourable natural course of these symptoms, as observed in the placebo groups. Due to the unfavourable balance between beneficial effects and risks of adverse events of the atypical antipsychotics, it is advised to look at alternative therapeutic options. Treatment of the underlying possible psychosocial and somatic causes of agitation or psychosis should always be considered.

References

  1. Mühlbauer V, Möhler R, Dichter MN et al. Antipsychotics for agitation and psychosis in people with Alzheimer's disease and vascular dementia. Cochrane Database Syst Rev 2021;(12):CD013304. «PMID: 34918337»PubMed