Anticonvulsants in the Treatment of Behavioral and Psychological Symptoms in Dementia: A Systematic Review.

Anticonvulsants BPSD carbamazepine dementia oxcarbazepine topiramate valproate

Journal

The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry
ISSN: 1545-7214
Titre abrégé: Am J Geriatr Psychiatry
Pays: England
ID NLM: 9309609

Informations de publication

Date de publication:
16 May 2024
Historique:
received: 18 11 2023
revised: 05 05 2024
accepted: 06 05 2024
medline: 14 6 2024
pubmed: 14 6 2024
entrez: 13 6 2024
Statut: aheadofprint

Résumé

Behavioral and psychological symptoms of dementia (BPSD) are common and impart a significant burden to patients, caregivers, and the health system. However, there are few pharmacological options for treating BPSD. We conducted a systematic review of clinical trials examining the efficacy of anticonvulsants in BPSD. We searched five electronic databases through January 2023, for randomized controlled trials and systematic reviews evaluating the efficacy of non-benzodiazepine anticonvulsants for the treatment of BPSD. We used the Cochrane risk of bias tool to ascertain the risk of bias in included trials. Because statistical pooling of results using meta-analysis was not feasible, we synthesized findings using the Cochrane Synthesis Without Meta-analysis reporting guidelines. We identified 12 studies, including randomized controlled trials (RCTs) and 1 systematic review. Five RCTs evaluating valproic acid were synthesized by a recent Cochrane review which concluded that this drug is likely ineffective for BPSD. We extracted data from 6 trials involving 248 individuals comparing non-benzodiazepine anticonvulsants to either placebo or risperidone. Four trials (n = 97 participants) evaluated carbamazepine, only one of which demonstrated an improvement in the Brief Psychiatric Rating Scale measuring agitation, hostility, psychosis, and withdrawal/depression (effect size: 1.13; 95% confidence interval [CI]: 0.54-1.73) relative to placebo. Adverse effects were more common in patients receiving carbamazepine (20/27; 74%) relative to placebo (5/24; 21%). There is low quality evidence that oxcarbazepine is likely ineffective and that topiramate may be comparable to risperidone. Anticonvulsants are unlikely to be effective in BPSD, although the quality of existing evidence is low.

Identifiants

pubmed: 38871629
pii: S1064-7481(24)00333-6
doi: 10.1016/j.jagp.2024.05.004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

DISCLOSURES The authors have no disclosures to report.

Auteurs

Sophiya Benjamin (S)

Department of Psychiatry and Behavioural Neurosciences (BS, SS), McMaster University, Hamilton, Ontario, Canada; Schlegel-UW Research Institute for Aging (BS, JM-W), Waterloo, Ontario, Canada; GeriMedRisk (BS, JM-W, TJ), Waterloo, Ontario, Canada. Electronic address: benjas@mcmaster.ca.

Joanne Man-Wai Ho (JM)

Schlegel-UW Research Institute for Aging (BS, JM-W), Waterloo, Ontario, Canada; GeriMedRisk (BS, JM-W, TJ), Waterloo, Ontario, Canada; Department of Medicine (JM-W), McMaster University, Waterloo, Ontario, Canada.

Jennifer Tung (J)

GeriMedRisk (BS, JM-W, TJ), Waterloo, Ontario, Canada; Grand River Hospital (TJ), Kitchener, Ontario, Canada.

Saumil Dholakia (S)

The Ottawa Hospital | L'Hôpital d'Ottawa (DS), Ottawa, Canada; University of Ottawa | l'Université d'Ottawa (DS), Ottawa, Canada.

Howard An (H)

Unity Health Toronto (AH), University of Toronto, Toronto, Ontario, Canada.

Tony Antoniou (T)

Department of Family and Community Medicine (AT), University of Toronto, Toronto, Ontario, Canada; Li Ka Shing Knowledge Institute (AT), St. Michael's Hospital, Toronto, Ontario, Canada.

Stephanie Sanger (S)

Department of Psychiatry and Behavioural Neurosciences (BS, SS), McMaster University, Hamilton, Ontario, Canada.

John W Williams (JW)

Division of General Internal Medicine (WJW), Duke University, Durham, NC.

Classifications MeSH