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An open-label, flexible-dose study of paliperidone extended-release in Chinese patients with first-onset psychosis

BACKGROUND: Antipsychotic medications facilitate the improvement of psychotic symptoms in patients with first-episode psychosis. Paliperidone extended-release (pali-ER), an atypical antipsychotic, was assessed for efficacy and safety in Chinese patients with first-episode psychosis. METHODS: In this...

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Autores principales: Si, TianMei, Tan, QingRong, Zhang, KeRang, Wang, Yang, Rui, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4295537/
https://www.ncbi.nlm.nih.gov/pubmed/25657581
http://dx.doi.org/10.2147/NDT.S70694
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author Si, TianMei
Tan, QingRong
Zhang, KeRang
Wang, Yang
Rui, Qing
author_facet Si, TianMei
Tan, QingRong
Zhang, KeRang
Wang, Yang
Rui, Qing
author_sort Si, TianMei
collection PubMed
description BACKGROUND: Antipsychotic medications facilitate the improvement of psychotic symptoms in patients with first-episode psychosis. Paliperidone extended-release (pali-ER), an atypical antipsychotic, was assessed for efficacy and safety in Chinese patients with first-episode psychosis. METHODS: In this 8-week, open-label, single-arm, multicenter study, patients with first-episode psychosis (Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition criteria) and a Positive and Negative Syndrome Scale (PANSS) total score ≥70 were treated with flexible-dose pali-ER tablets (3–12 mg/day). The primary efficacy endpoint was the percentage of patients with an increase of ≥8 points in Personal and Social Performance (PSP) score from baseline to day 56 (8 weeks). Secondary endpoints included reduction in PANSS total score, improvement in Clinical Global Impression-Severity score, PSP score, Subjective Well-being under Neuroleptics Scale score, and relationship between duration of untreated psychosis and PANSS or PSP. Incidences of treatment-emergent adverse events were used to evaluate safety. RESULTS: Overall, 283 of 294 patients (96%) achieved a ≥8-point increase in PSP (primary endpoint, analysis set). For the secondary efficacy endpoints, 284/306 patients (93%) had a ≥30% reduction in PANSS total score; 266/306 patients (87%) achieved a ≤3 Clinical Global Impression-Severity scale score, and 218/294 patients (74%) had a PSP score ≥71. The Subjective Well-being under Neuroleptics Scale score was improved from a baseline mean of 72.7 to 94.7 at endpoint. There was a negative correlation between duration of untreated psychosis and posttreatment PSP score and a positive correlation with posttreatment PANSS total score. The most common treatment-emergent adverse events were extrapyramidal symptoms (12%), and agitation, somnolence, and xerostomia (4% each). CONCLUSION: An 8-week, flexible-dose (3–12 mg/day) treatment with pali-ER resulted in significant improvements in psychotic symptoms and social functioning in Chinese patients with first-episode psychosis and was generally tolerable.
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spelling pubmed-42955372015-02-05 An open-label, flexible-dose study of paliperidone extended-release in Chinese patients with first-onset psychosis Si, TianMei Tan, QingRong Zhang, KeRang Wang, Yang Rui, Qing Neuropsychiatr Dis Treat Original Research BACKGROUND: Antipsychotic medications facilitate the improvement of psychotic symptoms in patients with first-episode psychosis. Paliperidone extended-release (pali-ER), an atypical antipsychotic, was assessed for efficacy and safety in Chinese patients with first-episode psychosis. METHODS: In this 8-week, open-label, single-arm, multicenter study, patients with first-episode psychosis (Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition criteria) and a Positive and Negative Syndrome Scale (PANSS) total score ≥70 were treated with flexible-dose pali-ER tablets (3–12 mg/day). The primary efficacy endpoint was the percentage of patients with an increase of ≥8 points in Personal and Social Performance (PSP) score from baseline to day 56 (8 weeks). Secondary endpoints included reduction in PANSS total score, improvement in Clinical Global Impression-Severity score, PSP score, Subjective Well-being under Neuroleptics Scale score, and relationship between duration of untreated psychosis and PANSS or PSP. Incidences of treatment-emergent adverse events were used to evaluate safety. RESULTS: Overall, 283 of 294 patients (96%) achieved a ≥8-point increase in PSP (primary endpoint, analysis set). For the secondary efficacy endpoints, 284/306 patients (93%) had a ≥30% reduction in PANSS total score; 266/306 patients (87%) achieved a ≤3 Clinical Global Impression-Severity scale score, and 218/294 patients (74%) had a PSP score ≥71. The Subjective Well-being under Neuroleptics Scale score was improved from a baseline mean of 72.7 to 94.7 at endpoint. There was a negative correlation between duration of untreated psychosis and posttreatment PSP score and a positive correlation with posttreatment PANSS total score. The most common treatment-emergent adverse events were extrapyramidal symptoms (12%), and agitation, somnolence, and xerostomia (4% each). CONCLUSION: An 8-week, flexible-dose (3–12 mg/day) treatment with pali-ER resulted in significant improvements in psychotic symptoms and social functioning in Chinese patients with first-episode psychosis and was generally tolerable. Dove Medical Press 2015-01-06 /pmc/articles/PMC4295537/ /pubmed/25657581 http://dx.doi.org/10.2147/NDT.S70694 Text en © 2015 Si et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Si, TianMei
Tan, QingRong
Zhang, KeRang
Wang, Yang
Rui, Qing
An open-label, flexible-dose study of paliperidone extended-release in Chinese patients with first-onset psychosis
title An open-label, flexible-dose study of paliperidone extended-release in Chinese patients with first-onset psychosis
title_full An open-label, flexible-dose study of paliperidone extended-release in Chinese patients with first-onset psychosis
title_fullStr An open-label, flexible-dose study of paliperidone extended-release in Chinese patients with first-onset psychosis
title_full_unstemmed An open-label, flexible-dose study of paliperidone extended-release in Chinese patients with first-onset psychosis
title_short An open-label, flexible-dose study of paliperidone extended-release in Chinese patients with first-onset psychosis
title_sort open-label, flexible-dose study of paliperidone extended-release in chinese patients with first-onset psychosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4295537/
https://www.ncbi.nlm.nih.gov/pubmed/25657581
http://dx.doi.org/10.2147/NDT.S70694
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