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Cariprazine in Three Acute Patients with Schizophrenia: A Real-World Experience

There are still some unmet needs in the treatment of schizophrenia like the persistence of negative symptoms. Cariprazine is a new-generation antipsychotic with partial agonism of the dopamine receptors, distinct from other antipsychotics by its 10 times greater affinity for D3 receptors. This mecha...

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Autores principales: Montes, Jose M, Montes, Paloma, Hernández-Huerta, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868213/
https://www.ncbi.nlm.nih.gov/pubmed/33568908
http://dx.doi.org/10.2147/NDT.S298005
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author Montes, Jose M
Montes, Paloma
Hernández-Huerta, Daniel
author_facet Montes, Jose M
Montes, Paloma
Hernández-Huerta, Daniel
author_sort Montes, Jose M
collection PubMed
description There are still some unmet needs in the treatment of schizophrenia like the persistence of negative symptoms. Cariprazine is a new-generation antipsychotic with partial agonism of the dopamine receptors, distinct from other antipsychotics by its 10 times greater affinity for D3 receptors. This mechanism of action could be especially favorable on patients with predominant negative symptoms. This report is showing three clinical cases of acute schizophrenia exacerbation that required hospitalization and were successfully treated with cariprazine. All of them had predominant positive symptoms and two of them had substance use. Efficacy of cariprazine was also crucial on negative and cognitive symptoms with excellent tolerability.
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spelling pubmed-78682132021-02-09 Cariprazine in Three Acute Patients with Schizophrenia: A Real-World Experience Montes, Jose M Montes, Paloma Hernández-Huerta, Daniel Neuropsychiatr Dis Treat Case Series There are still some unmet needs in the treatment of schizophrenia like the persistence of negative symptoms. Cariprazine is a new-generation antipsychotic with partial agonism of the dopamine receptors, distinct from other antipsychotics by its 10 times greater affinity for D3 receptors. This mechanism of action could be especially favorable on patients with predominant negative symptoms. This report is showing three clinical cases of acute schizophrenia exacerbation that required hospitalization and were successfully treated with cariprazine. All of them had predominant positive symptoms and two of them had substance use. Efficacy of cariprazine was also crucial on negative and cognitive symptoms with excellent tolerability. Dove 2021-02-03 /pmc/articles/PMC7868213/ /pubmed/33568908 http://dx.doi.org/10.2147/NDT.S298005 Text en © 2021 Montes et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Case Series
Montes, Jose M
Montes, Paloma
Hernández-Huerta, Daniel
Cariprazine in Three Acute Patients with Schizophrenia: A Real-World Experience
title Cariprazine in Three Acute Patients with Schizophrenia: A Real-World Experience
title_full Cariprazine in Three Acute Patients with Schizophrenia: A Real-World Experience
title_fullStr Cariprazine in Three Acute Patients with Schizophrenia: A Real-World Experience
title_full_unstemmed Cariprazine in Three Acute Patients with Schizophrenia: A Real-World Experience
title_short Cariprazine in Three Acute Patients with Schizophrenia: A Real-World Experience
title_sort cariprazine in three acute patients with schizophrenia: a real-world experience
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868213/
https://www.ncbi.nlm.nih.gov/pubmed/33568908
http://dx.doi.org/10.2147/NDT.S298005
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