A randomized controlled trial of quetiapine for psychosis in Parkinson’s disease

Paul Shotbolt1, Michael Samuel2,3, Chris Fox3,4, Anthony S David11Section of Cognitive Neuropsychiatry, Institute of Psychiatry, King’s College, London, UK; 2Department of Neurology, King’s College hospital, London, UK; 3East Kent hospitals NHS Trust, William Harvey Hospi...

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Autores principales: Paul Shotbolt, Michael Samuel, Chris Fox, Anthony S David
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Publicado: Dove Medical Press 2009
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spelling oai:doaj.org-article:6e587c3603b044e4b2a262c0049051092021-12-02T03:44:12ZA randomized controlled trial of quetiapine for psychosis in Parkinson’s disease1176-63281178-2021https://doaj.org/article/6e587c3603b044e4b2a262c0049051092009-05-01T00:00:00Zhttp://www.dovepress.com/a-randomized-controlled-trial-of-quetiapine-for-psychosis-in-parkinson-a3162https://doaj.org/toc/1176-6328https://doaj.org/toc/1178-2021Paul Shotbolt1, Michael Samuel2,3, Chris Fox3,4, Anthony S David11Section of Cognitive Neuropsychiatry, Institute of Psychiatry, King’s College, London, UK; 2Department of Neurology, King’s College hospital, London, UK; 3East Kent hospitals NHS Trust, William Harvey Hospital, Ashford, Kent, UK; 4Kent and Medway NHS and Social Care and Partnership Trust, Kent, UKIntroduction: Psychosis (delusions and/or hallucinations) is a well-recognized complication of treatment of Parkinson’s disease (PD). Quetiapine is a currently favored treatment, but data on its efficacy are equivocal. This trial aimed to provide further evidence on the efficacy of quetiapine in PD psychosis.Methods: We conducted a 12 week double blind randomized placebo-controlled trial. Time to dropout due to lack of improvement of psychosis was the primary outcome measure. Other important secondary outcomes were evaluated using standard rating scales for PD and psychiatric symptoms.Results: Twenty-four eligible subjects gave consent. The primary outcome, time to dropout, was examined using survival analysis. It was shown that patients in the quetiapine group dropped out earlier than those in the placebo group, but this difference was not significant (p = 0.68). No significant changes were found for any of the secondary outcome measures in either group. Conclusions: In this study, quetiapine at doses of up to 150 mg/day failed to significantly improve psychosis compared to placebo, however the small sample size does not allow any conclusive interpretation of the results. Quetiapine did not appear to worsen PD motor functioning, but its use was limited by a faster drop out compared with placebo. Significant impediments were difficulty with recruitment and natural fluctuation in symptoms during the trial. Keywords: Parkinson’s disease, psychosis, antipsychotics, quetiapine Paul ShotboltMichael SamuelChris FoxAnthony S DavidDove Medical PressarticleNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571Neurology. Diseases of the nervous systemRC346-429ENNeuropsychiatric Disease and Treatment, Vol 2009, Iss default, Pp 327-332 (2009)
institution DOAJ
collection DOAJ
language EN
topic Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
spellingShingle Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
Paul Shotbolt
Michael Samuel
Chris Fox
Anthony S David
A randomized controlled trial of quetiapine for psychosis in Parkinson’s disease
description Paul Shotbolt1, Michael Samuel2,3, Chris Fox3,4, Anthony S David11Section of Cognitive Neuropsychiatry, Institute of Psychiatry, King’s College, London, UK; 2Department of Neurology, King’s College hospital, London, UK; 3East Kent hospitals NHS Trust, William Harvey Hospital, Ashford, Kent, UK; 4Kent and Medway NHS and Social Care and Partnership Trust, Kent, UKIntroduction: Psychosis (delusions and/or hallucinations) is a well-recognized complication of treatment of Parkinson’s disease (PD). Quetiapine is a currently favored treatment, but data on its efficacy are equivocal. This trial aimed to provide further evidence on the efficacy of quetiapine in PD psychosis.Methods: We conducted a 12 week double blind randomized placebo-controlled trial. Time to dropout due to lack of improvement of psychosis was the primary outcome measure. Other important secondary outcomes were evaluated using standard rating scales for PD and psychiatric symptoms.Results: Twenty-four eligible subjects gave consent. The primary outcome, time to dropout, was examined using survival analysis. It was shown that patients in the quetiapine group dropped out earlier than those in the placebo group, but this difference was not significant (p = 0.68). No significant changes were found for any of the secondary outcome measures in either group. Conclusions: In this study, quetiapine at doses of up to 150 mg/day failed to significantly improve psychosis compared to placebo, however the small sample size does not allow any conclusive interpretation of the results. Quetiapine did not appear to worsen PD motor functioning, but its use was limited by a faster drop out compared with placebo. Significant impediments were difficulty with recruitment and natural fluctuation in symptoms during the trial. Keywords: Parkinson’s disease, psychosis, antipsychotics, quetiapine
format article
author Paul Shotbolt
Michael Samuel
Chris Fox
Anthony S David
author_facet Paul Shotbolt
Michael Samuel
Chris Fox
Anthony S David
author_sort Paul Shotbolt
title A randomized controlled trial of quetiapine for psychosis in Parkinson’s disease
title_short A randomized controlled trial of quetiapine for psychosis in Parkinson’s disease
title_full A randomized controlled trial of quetiapine for psychosis in Parkinson’s disease
title_fullStr A randomized controlled trial of quetiapine for psychosis in Parkinson’s disease
title_full_unstemmed A randomized controlled trial of quetiapine for psychosis in Parkinson’s disease
title_sort randomized controlled trial of quetiapine for psychosis in parkinson’s disease
publisher Dove Medical Press
publishDate 2009
url https://doaj.org/article/6e587c3603b044e4b2a262c004905109
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