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Second International Consensus Study of Antipsychotic Dosing (ICSAD-2)

BACKGROUND: Expert consensus-based clinically equivalent dose estimates and dosing recommendations can provide valuable support for the use of drugs for psychosis in clinical practice and research. AIMS: This second International Consensus Study of Antipsychotic Dosing provides dosing equivalencies...

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Autores principales: McAdam, Matthew KT, Baldessarini, Ross J, Murphy, Andrea L, Gardner, David M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10612374/
https://www.ncbi.nlm.nih.gov/pubmed/37842908
http://dx.doi.org/10.1177/02698811231205688
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author McAdam, Matthew KT
Baldessarini, Ross J
Murphy, Andrea L
Gardner, David M
author_facet McAdam, Matthew KT
Baldessarini, Ross J
Murphy, Andrea L
Gardner, David M
author_sort McAdam, Matthew KT
collection PubMed
description BACKGROUND: Expert consensus-based clinically equivalent dose estimates and dosing recommendations can provide valuable support for the use of drugs for psychosis in clinical practice and research. AIMS: This second International Consensus Study of Antipsychotic Dosing provides dosing equivalencies and recommendations for newer drugs for psychosis and previously reported drugs with low consensus. METHODS: We used a two-step Delphi survey process to establish and update consensus with a broad, international sample of clinical and research experts regarding 26 drug formulations to obtain dosing recommendations (start, target range, and maximum) and estimates of clinically equivalent doses for the treatment of schizophrenia. Reference agents for equivalent dose estimates were oral olanzapine 20 mg/day for 15 oral and 7 long-acting injectable (LAI) agents and intramuscular haloperidol 5 mg for 4 short-acting injectable (SAI) agents. We also provide a contemporary list of equivalency estimates and dosing recommendations for a total of 44 oral, 16 LAI, and 14 SAI drugs for psychosis. RESULTS: Survey participants (N = 72) from 24 countries provided equivalency estimates and dosing recommendations for oral, LAI, and SAI formulations. Consensus improved from survey stages I to II. The final consensus was highest for LAI formulations, intermediate for oral agents, and lowest for SAI formulations of drugs for psychosis. CONCLUSIONS: As randomized, controlled, fixed, multiple-dose trials to optimize the dosing of drugs for psychosis remain rare, expert consensus remains a useful alternative for estimating clinical dosing equivalents. The present findings can support clinical practice, guideline development, and research design and interpretation involving drugs for psychosis.
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spelling pubmed-106123742023-10-29 Second International Consensus Study of Antipsychotic Dosing (ICSAD-2) McAdam, Matthew KT Baldessarini, Ross J Murphy, Andrea L Gardner, David M J Psychopharmacol Original Papers BACKGROUND: Expert consensus-based clinically equivalent dose estimates and dosing recommendations can provide valuable support for the use of drugs for psychosis in clinical practice and research. AIMS: This second International Consensus Study of Antipsychotic Dosing provides dosing equivalencies and recommendations for newer drugs for psychosis and previously reported drugs with low consensus. METHODS: We used a two-step Delphi survey process to establish and update consensus with a broad, international sample of clinical and research experts regarding 26 drug formulations to obtain dosing recommendations (start, target range, and maximum) and estimates of clinically equivalent doses for the treatment of schizophrenia. Reference agents for equivalent dose estimates were oral olanzapine 20 mg/day for 15 oral and 7 long-acting injectable (LAI) agents and intramuscular haloperidol 5 mg for 4 short-acting injectable (SAI) agents. We also provide a contemporary list of equivalency estimates and dosing recommendations for a total of 44 oral, 16 LAI, and 14 SAI drugs for psychosis. RESULTS: Survey participants (N = 72) from 24 countries provided equivalency estimates and dosing recommendations for oral, LAI, and SAI formulations. Consensus improved from survey stages I to II. The final consensus was highest for LAI formulations, intermediate for oral agents, and lowest for SAI formulations of drugs for psychosis. CONCLUSIONS: As randomized, controlled, fixed, multiple-dose trials to optimize the dosing of drugs for psychosis remain rare, expert consensus remains a useful alternative for estimating clinical dosing equivalents. The present findings can support clinical practice, guideline development, and research design and interpretation involving drugs for psychosis. SAGE Publications 2023-10-16 2023-10 /pmc/articles/PMC10612374/ /pubmed/37842908 http://dx.doi.org/10.1177/02698811231205688 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Papers
McAdam, Matthew KT
Baldessarini, Ross J
Murphy, Andrea L
Gardner, David M
Second International Consensus Study of Antipsychotic Dosing (ICSAD-2)
title Second International Consensus Study of Antipsychotic Dosing (ICSAD-2)
title_full Second International Consensus Study of Antipsychotic Dosing (ICSAD-2)
title_fullStr Second International Consensus Study of Antipsychotic Dosing (ICSAD-2)
title_full_unstemmed Second International Consensus Study of Antipsychotic Dosing (ICSAD-2)
title_short Second International Consensus Study of Antipsychotic Dosing (ICSAD-2)
title_sort second international consensus study of antipsychotic dosing (icsad-2)
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10612374/
https://www.ncbi.nlm.nih.gov/pubmed/37842908
http://dx.doi.org/10.1177/02698811231205688
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