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Continuation rate for asenapine and brexpiprazole treatment in patients with schizophrenia

INTRODUCTION: The current study sought to compare the treatment continuation rates of asenapine and brexpiprazole while specifically investigating the factors influencing this index and the clinical efficacy of brexpiprazole. METHODS: Retrospective study on patients with schizophrenia who were presc...

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Autores principales: Inoue, Yuichi, Suzuki, Hidenobu, Hibino, Hiroyuki, Takaya, Atsuhiko, Mikami, Katsunaka, Yamamoto, Kenji, Matsumoto, Hideo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119821/
https://www.ncbi.nlm.nih.gov/pubmed/33713580
http://dx.doi.org/10.1002/brb3.2109
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author Inoue, Yuichi
Suzuki, Hidenobu
Hibino, Hiroyuki
Takaya, Atsuhiko
Mikami, Katsunaka
Yamamoto, Kenji
Matsumoto, Hideo
author_facet Inoue, Yuichi
Suzuki, Hidenobu
Hibino, Hiroyuki
Takaya, Atsuhiko
Mikami, Katsunaka
Yamamoto, Kenji
Matsumoto, Hideo
author_sort Inoue, Yuichi
collection PubMed
description INTRODUCTION: The current study sought to compare the treatment continuation rates of asenapine and brexpiprazole while specifically investigating the factors influencing this index and the clinical efficacy of brexpiprazole. METHODS: Retrospective study on patients with schizophrenia who were prescribed either asenapine (n = 73) or brexpiprazole (n = 136), as part of their routine medical care. RESULTS: The treatment continuation rates for asenapine and brexpiprazole were 19.0% and 38.6% at 52 weeks, with that of brexpiprazole found to be significantly higher than that of asenapine (p = .002). Moreover, age was found to be a significant factor affecting the treatment continuation rate for brexpiprazole (p = .03). Additionally, patients with a longer continuation duration had significantly lower Clinical Global Impression‐Severity of Illness (CGI‐S) scale scores compared to those who discontinued early (p = .04). The continuation rate was also significantly higher for those who began using the drug as outpatients compared to those first administered the drug as inpatients (p = .04). Furthermore, disease duration, CGI‐S scale, and continuation duration significantly affected the clinical efficacy of brexipiprazole (p < .05 for all). CONCLUSIONS: The continuation rate for brexpiprazole increases as the age of the patient increases, as disease severity decreases, and if the patient first uses the drug as an outpatient. Shorter disease duration and longer drug administration may lead to improved clinical efficacy. These results suggest that brexpiprazole is an effective treatment option for maintenance therapy of schizophrenia.
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spelling pubmed-81198212021-05-20 Continuation rate for asenapine and brexpiprazole treatment in patients with schizophrenia Inoue, Yuichi Suzuki, Hidenobu Hibino, Hiroyuki Takaya, Atsuhiko Mikami, Katsunaka Yamamoto, Kenji Matsumoto, Hideo Brain Behav Original Research INTRODUCTION: The current study sought to compare the treatment continuation rates of asenapine and brexpiprazole while specifically investigating the factors influencing this index and the clinical efficacy of brexpiprazole. METHODS: Retrospective study on patients with schizophrenia who were prescribed either asenapine (n = 73) or brexpiprazole (n = 136), as part of their routine medical care. RESULTS: The treatment continuation rates for asenapine and brexpiprazole were 19.0% and 38.6% at 52 weeks, with that of brexpiprazole found to be significantly higher than that of asenapine (p = .002). Moreover, age was found to be a significant factor affecting the treatment continuation rate for brexpiprazole (p = .03). Additionally, patients with a longer continuation duration had significantly lower Clinical Global Impression‐Severity of Illness (CGI‐S) scale scores compared to those who discontinued early (p = .04). The continuation rate was also significantly higher for those who began using the drug as outpatients compared to those first administered the drug as inpatients (p = .04). Furthermore, disease duration, CGI‐S scale, and continuation duration significantly affected the clinical efficacy of brexipiprazole (p < .05 for all). CONCLUSIONS: The continuation rate for brexpiprazole increases as the age of the patient increases, as disease severity decreases, and if the patient first uses the drug as an outpatient. Shorter disease duration and longer drug administration may lead to improved clinical efficacy. These results suggest that brexpiprazole is an effective treatment option for maintenance therapy of schizophrenia. John Wiley and Sons Inc. 2021-03-13 /pmc/articles/PMC8119821/ /pubmed/33713580 http://dx.doi.org/10.1002/brb3.2109 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Inoue, Yuichi
Suzuki, Hidenobu
Hibino, Hiroyuki
Takaya, Atsuhiko
Mikami, Katsunaka
Yamamoto, Kenji
Matsumoto, Hideo
Continuation rate for asenapine and brexpiprazole treatment in patients with schizophrenia
title Continuation rate for asenapine and brexpiprazole treatment in patients with schizophrenia
title_full Continuation rate for asenapine and brexpiprazole treatment in patients with schizophrenia
title_fullStr Continuation rate for asenapine and brexpiprazole treatment in patients with schizophrenia
title_full_unstemmed Continuation rate for asenapine and brexpiprazole treatment in patients with schizophrenia
title_short Continuation rate for asenapine and brexpiprazole treatment in patients with schizophrenia
title_sort continuation rate for asenapine and brexpiprazole treatment in patients with schizophrenia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119821/
https://www.ncbi.nlm.nih.gov/pubmed/33713580
http://dx.doi.org/10.1002/brb3.2109
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