4.6 Article

Antipsychotic use in dementia: the relationship between neuropsychiatric symptom profiles and adverse outcomes

Journal

EUROPEAN JOURNAL OF EPIDEMIOLOGY
Volume 36, Issue 1, Pages 89-101

Publisher

SPRINGER
DOI: 10.1007/s10654-020-00643-2

Keywords

Dementia; Antipsychotics; Risk stratification; Prognosis; Mortality; Stroke

Funding

  1. EPSRC [EP/N027280/1] Funding Source: UKRI
  2. MRC [MC_PC_17214] Funding Source: UKRI

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This study found that antipsychotic prescriptions in patients with dementia, specifically those with psychosis but no agitation, may increase the risk of hospitalised stroke. Overall, antipsychotic use was also associated with an increased risk of all-cause mortality and stroke-specific mortality in the sample.
Antipsychotic treatments are associated with safety concerns in people with dementia. The authors aimed to investigate whether risk of adverse outcomes related to antipsychotic prescribing differed according to major neuropsychiatric syndromes-specifically psychosis, agitation, or a combination. A cohort of 10,106 patients with a diagnosis of dementia was assembled from a large dementia care database in South East London. Neuropsychiatric symptoms closest to first dementia diagnosis were determined according to the Health of the Nation Outcome Scales' mental and behavioural problem scores and the sample was divided into four groups: 'agitation and psychosis', 'agitation, but no psychosis', 'psychosis, but no agitation', and 'neither psychosis nor agitation'. Antipsychotic prescription in a one-year window around first dementia diagnosis was ascertained as exposure variable through natural language processing from free text. Cox regression models were used to analyse associations of antipsychotic prescription with all-cause and stroke-specific mortality, emergency hospitalisation and hospitalised stroke adjusting for sixteen potential confounders including demographics, cognition, functioning, as well as physical and mental health. Only in the group 'psychosis, but no agitation' (n = 579), 30% of whom were prescribed an antipsychotic, a significant antipsychotic-associated increased risk of hospitalised stroke was present after adjustment (adjusted hazard ratio (HR) 2.16; 95% confidence interval (CI) 1.09-4.25). An increased antipsychotic-related all-cause (adjusted HR 1.14; 95% CI 1.04-1.24) and stroke-specific mortality risk (adjusted HR 1.28; 95% CI 1.01-1.63) was detected in the whole sample, but no interaction between the strata and antipsychotic-related mortality. In conclusion, the adverse effects of antipsychotics in dementia are complex. Stroke risk may be highest when used in patients presenting with psychosis without agitation, indicating the need for novel interventions for this group.

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