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Study of mirtazapine for agitated behaviours in dementia (SYMBAD): a randomised, double-blind, placebo-controlled trial.
Banerjee, Sube; High, Juliet; Stirling, Susan; Shepstone, Lee; Swart, Ann Marie; Telling, Tanya; Henderson, Catherine; Ballard, Clive; Bentham, Peter; Burns, Alistair; Farina, Nicolas; Fox, Chris; Francis, Paul; Howard, Robert; Knapp, Martin; Leroi, Iracema; Livingston, Gill; Nilforooshan, Ramin; Nurock, Shirley; O'Brien, John; Price, Annabel; Thomas, Alan J; Tabet, Naji.
Afiliación
  • Banerjee S; Faculty of Health, University of Plymouth, Plymouth, UK. Electronic address: sube.banerjee@plymouth.ac.uk.
  • High J; Norwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
  • Stirling S; Norwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
  • Shepstone L; Norwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
  • Swart AM; Norwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
  • Telling T; Joint Clinical Research Office, University of Sussex, Brighton, UK.
  • Henderson C; Care Policy and Evaluation Centre, London School of Economics and Political Science, London, UK.
  • Ballard C; College of Medicine and Health, University of Exeter, Exeter, UK.
  • Bentham P; Birmingham and Solihull Mental Health Foundation NHS Trust, Birmingham, UK.
  • Burns A; University of Manchester, Manchester, UK.
  • Farina N; Centre for Dementia Studies, Brighton and Sussex Medical School, University of Sussex, Brighton, UK.
  • Fox C; Norwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
  • Francis P; College of Medicine and Health, University of Exeter, Exeter, UK.
  • Howard R; Division of Psychiatry, University College London, London, UK.
  • Knapp M; Care Policy and Evaluation Centre, London School of Economics and Political Science, London, UK.
  • Leroi I; Department of Psychiatry, Global Brain Health Institute, Trinity College, Dublin, Ireland.
  • Livingston G; Division of Psychiatry, University College London, London, UK.
  • Nilforooshan R; Surrey and Borders Partnership NHS Foundation Trust, Leatherhead, UK.
  • Nurock S; Former Carer, Alzheimer's Society Research Network, University of Cambridge School of Medicine, Cambridge, UK.
  • O'Brien J; Department of Psychiatry, University of Cambridge School of Medicine, Cambridge, UK.
  • Price A; Cambridgeshire and Peterborough Foundation Trust, Cambridge, UK.
  • Thomas AJ; Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Tabet N; Centre for Dementia Studies, Brighton and Sussex Medical School, University of Sussex, Brighton, UK.
Lancet ; 398(10310): 1487-1497, 2021 10 23.
Article en En | MEDLINE | ID: mdl-34688369
ABSTRACT

BACKGROUND:

Agitation is common in people with dementia and negatively affects the quality of life of both people with dementia and carers. Non-drug patient-centred care is the first-line treatment, but there is a need for other treatment when this care is not effective. Current evidence is sparse on safer and effective alternatives to antipsychotics. We assessed the efficacy and safety of mirtazapine, an antidepressant prescribed for agitation in dementia.

METHODS:

This parallel-group, double-blind, placebo-controlled trial-the Study of Mirtazapine for Agitated Behaviours in Dementia trial (SYMBAD)-was done in 26 UK centres. Participants had probable or possible Alzheimer's disease, agitation unresponsive to non-drug treatment, and a Cohen-Mansfield Agitation Inventory (CMAI) score of 45 or more. They were randomly assigned (11) to receive either mirtazapine (titrated to 45 mg) or placebo. The primary outcome was reduction in CMAI score at 12 weeks. This trial is registered with ClinicalTrials.gov, NCT03031184, and ISRCTN17411897.

FINDINGS:

Between Jan 26, 2017, and March 6, 2020, 204 participants were recruited and randomised. Mean CMAI scores at 12 weeks were not significantly different between participants receiving mirtazapine and participants receiving placebo (adjusted mean difference -1·74, 95% CI -7·17 to 3·69; p=0·53). The number of controls with adverse events (65 [64%] of 102 controls) was similar to that in the mirtazapine group (67 [66%] of 102 participants receiving mirtazapine). However, there were more deaths in the mirtazapine group (n=7) by week 16 than in the control group (n=1), with post-hoc analysis suggesting this difference was of marginal statistical significance (p=0·065).

INTERPRETATION:

This trial found no benefit of mirtazapine compared with placebo, and we observed a potentially higher mortality with use of mirtazapine. The data from this study do not support using mirtazapine as a treatment for agitation in dementia.

FUNDING:

UK National Institute for Health Research Health Technology Assessment Programme.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Agitación Psicomotora / Ansiolíticos / Demencia / Mirtazapina Tipo de estudio: Clinical_trials / Health_technology_assessment Límite: Aged80 / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Lancet Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Agitación Psicomotora / Ansiolíticos / Demencia / Mirtazapina Tipo de estudio: Clinical_trials / Health_technology_assessment Límite: Aged80 / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Lancet Año: 2021 Tipo del documento: Article