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Clozapine once- versus multiple-daily dosing: a two-center cross-sectional study, systematic review and meta-analysis

Evidence regarding effectiveness and safety of clozapine once- vs. multiple-daily dosing is limited. We compared demographic and clinical parameters between patients with once- vs. multiple-daily dosing in the Department of Psychiatry and Psychotherapy, University of Regensburg, Germany (AGATE datas...

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Autores principales: Kuzo, Nazar, Haen, Ekkehard, Ho, Dominic M., Takeuchi, Hiroyoshi, Piras, Marianna, Eap, Chin-Bin, de Filippis, Renato, Homan, Philipp, Kane, John M., Roy, Marc-André, Paulzen, Michael, Schoretsanitis, Georgios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465369/
https://www.ncbi.nlm.nih.gov/pubmed/36580106
http://dx.doi.org/10.1007/s00406-022-01542-1
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author Kuzo, Nazar
Haen, Ekkehard
Ho, Dominic M.
Takeuchi, Hiroyoshi
Piras, Marianna
Eap, Chin-Bin
de Filippis, Renato
Homan, Philipp
Kane, John M.
Roy, Marc-André
Paulzen, Michael
Schoretsanitis, Georgios
author_facet Kuzo, Nazar
Haen, Ekkehard
Ho, Dominic M.
Takeuchi, Hiroyoshi
Piras, Marianna
Eap, Chin-Bin
de Filippis, Renato
Homan, Philipp
Kane, John M.
Roy, Marc-André
Paulzen, Michael
Schoretsanitis, Georgios
author_sort Kuzo, Nazar
collection PubMed
description Evidence regarding effectiveness and safety of clozapine once- vs. multiple-daily dosing is limited. We compared demographic and clinical parameters between patients with once- vs. multiple-daily dosing in the Department of Psychiatry and Psychotherapy, University of Regensburg, Germany (AGATE dataset), and the Department of Psychiatry, Lausanne University Hospital, Switzerland, using non-parametric tests. Effectiveness and safety outcomes were available in the AGATE dataset. We performed a systematic review in PubMed/Embase until February 2022, meta-analyzing studies comparing clozapine once- vs. multiple-daily-dosing. We estimated a pooled odds ratio for adverse drug-induced reactions (ADRs) and meta-analyzed differences regarding clinical symptom severity, age, percentage males, smokers, clozapine dose, and co-medications between patients receiving once- vs. multiple-daily dosing. Study quality was assessed using the Newcastle–Ottawa-Scale. Of 1494 and 174 patients included in AGATE and Lausanne datasets, clozapine was prescribed multiple-daily in 74.8% and 67.8%, respectively. In the AGATE cohort, no differences were reported for the clinical symptoms severity or ADR rate (p > 0.05). Meta-analyzing eight cohorts with a total of 2810 clozapine-treated individuals, we found more severe clinical symptoms (p = 0.036), increased ADR risk (p = 0.01), higher clozapine doses (p < 0.001), more frequent co-medication with other antipsychotics (p < 0.001), benzodiazepines (p < 0.001), anticholinergics (p = 0.039), and laxatives (p < 0.001) in patients on multiple- vs. once-daily dosing. Of six studies, five were rated as good, and one as poor quality. Patients responding less well to clozapine may be prescribed higher doses multiple-daily, also treated with polypharmacy, potentially underlying worse safety outcomes. Patient preferences and adherence should be considered during regimen selection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00406-022-01542-1.
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spelling pubmed-104653692023-08-31 Clozapine once- versus multiple-daily dosing: a two-center cross-sectional study, systematic review and meta-analysis Kuzo, Nazar Haen, Ekkehard Ho, Dominic M. Takeuchi, Hiroyoshi Piras, Marianna Eap, Chin-Bin de Filippis, Renato Homan, Philipp Kane, John M. Roy, Marc-André Paulzen, Michael Schoretsanitis, Georgios Eur Arch Psychiatry Clin Neurosci Original Paper Evidence regarding effectiveness and safety of clozapine once- vs. multiple-daily dosing is limited. We compared demographic and clinical parameters between patients with once- vs. multiple-daily dosing in the Department of Psychiatry and Psychotherapy, University of Regensburg, Germany (AGATE dataset), and the Department of Psychiatry, Lausanne University Hospital, Switzerland, using non-parametric tests. Effectiveness and safety outcomes were available in the AGATE dataset. We performed a systematic review in PubMed/Embase until February 2022, meta-analyzing studies comparing clozapine once- vs. multiple-daily-dosing. We estimated a pooled odds ratio for adverse drug-induced reactions (ADRs) and meta-analyzed differences regarding clinical symptom severity, age, percentage males, smokers, clozapine dose, and co-medications between patients receiving once- vs. multiple-daily dosing. Study quality was assessed using the Newcastle–Ottawa-Scale. Of 1494 and 174 patients included in AGATE and Lausanne datasets, clozapine was prescribed multiple-daily in 74.8% and 67.8%, respectively. In the AGATE cohort, no differences were reported for the clinical symptoms severity or ADR rate (p > 0.05). Meta-analyzing eight cohorts with a total of 2810 clozapine-treated individuals, we found more severe clinical symptoms (p = 0.036), increased ADR risk (p = 0.01), higher clozapine doses (p < 0.001), more frequent co-medication with other antipsychotics (p < 0.001), benzodiazepines (p < 0.001), anticholinergics (p = 0.039), and laxatives (p < 0.001) in patients on multiple- vs. once-daily dosing. Of six studies, five were rated as good, and one as poor quality. Patients responding less well to clozapine may be prescribed higher doses multiple-daily, also treated with polypharmacy, potentially underlying worse safety outcomes. Patient preferences and adherence should be considered during regimen selection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00406-022-01542-1. Springer Berlin Heidelberg 2022-12-29 2023 /pmc/articles/PMC10465369/ /pubmed/36580106 http://dx.doi.org/10.1007/s00406-022-01542-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Kuzo, Nazar
Haen, Ekkehard
Ho, Dominic M.
Takeuchi, Hiroyoshi
Piras, Marianna
Eap, Chin-Bin
de Filippis, Renato
Homan, Philipp
Kane, John M.
Roy, Marc-André
Paulzen, Michael
Schoretsanitis, Georgios
Clozapine once- versus multiple-daily dosing: a two-center cross-sectional study, systematic review and meta-analysis
title Clozapine once- versus multiple-daily dosing: a two-center cross-sectional study, systematic review and meta-analysis
title_full Clozapine once- versus multiple-daily dosing: a two-center cross-sectional study, systematic review and meta-analysis
title_fullStr Clozapine once- versus multiple-daily dosing: a two-center cross-sectional study, systematic review and meta-analysis
title_full_unstemmed Clozapine once- versus multiple-daily dosing: a two-center cross-sectional study, systematic review and meta-analysis
title_short Clozapine once- versus multiple-daily dosing: a two-center cross-sectional study, systematic review and meta-analysis
title_sort clozapine once- versus multiple-daily dosing: a two-center cross-sectional study, systematic review and meta-analysis
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465369/
https://www.ncbi.nlm.nih.gov/pubmed/36580106
http://dx.doi.org/10.1007/s00406-022-01542-1
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