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Optimizing dosing in atypical neuroleptic monotherapy

Atypical neuroleptics have become the first line of treatment for psychotic disorders, but some questions remain: what are their optimal dosages and is more medication more efficacious? For clozapine, it is recommended to aim for a plasma level above 350 ng/mL for nonresponders and partial responder...

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Detalles Bibliográficos
Autores principales: Trémeau, Fabien, Citrome, Leslie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Les Laboratoires Servier 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181693/
https://www.ncbi.nlm.nih.gov/pubmed/22033705
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author Trémeau, Fabien
Citrome, Leslie
author_facet Trémeau, Fabien
Citrome, Leslie
author_sort Trémeau, Fabien
collection PubMed
description Atypical neuroleptics have become the first line of treatment for psychotic disorders, but some questions remain: what are their optimal dosages and is more medication more efficacious? For clozapine, it is recommended to aim for a plasma level above 350 ng/mL for nonresponders and partial responders. It should be specified that this plasma level should be obtained exactly 12 h after the last dose. For risperidone, optimal daily doses range between 4 and 8 mg, and there is no indication that a higher dose would bring additional improvement. For olanzapine, a quite different situation is encountered. There is a good indication that daily doses of 30 and 40 mg can increase clinical response. It appears that plasma levels above 23 ng/mL may predict response. For quetiapine, reports on the utility of dosages greater than 800 mg/day are anecdotal at this point, and more studies should be conducted. For ziprasidone, dosages above 40 mg/day should be used, but daily doses above 200 mg have not yet been systematically investigated.
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spelling pubmed-31816932011-10-27 Optimizing dosing in atypical neuroleptic monotherapy Trémeau, Fabien Citrome, Leslie Dialogues Clin Neurosci Pharmacological Aspects Atypical neuroleptics have become the first line of treatment for psychotic disorders, but some questions remain: what are their optimal dosages and is more medication more efficacious? For clozapine, it is recommended to aim for a plasma level above 350 ng/mL for nonresponders and partial responders. It should be specified that this plasma level should be obtained exactly 12 h after the last dose. For risperidone, optimal daily doses range between 4 and 8 mg, and there is no indication that a higher dose would bring additional improvement. For olanzapine, a quite different situation is encountered. There is a good indication that daily doses of 30 and 40 mg can increase clinical response. It appears that plasma levels above 23 ng/mL may predict response. For quetiapine, reports on the utility of dosages greater than 800 mg/day are anecdotal at this point, and more studies should be conducted. For ziprasidone, dosages above 40 mg/day should be used, but daily doses above 200 mg have not yet been systematically investigated. Les Laboratoires Servier 2002-12 /pmc/articles/PMC3181693/ /pubmed/22033705 Text en Copyright: © 2002 LLS http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Pharmacological Aspects
Trémeau, Fabien
Citrome, Leslie
Optimizing dosing in atypical neuroleptic monotherapy
title Optimizing dosing in atypical neuroleptic monotherapy
title_full Optimizing dosing in atypical neuroleptic monotherapy
title_fullStr Optimizing dosing in atypical neuroleptic monotherapy
title_full_unstemmed Optimizing dosing in atypical neuroleptic monotherapy
title_short Optimizing dosing in atypical neuroleptic monotherapy
title_sort optimizing dosing in atypical neuroleptic monotherapy
topic Pharmacological Aspects
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181693/
https://www.ncbi.nlm.nih.gov/pubmed/22033705
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