Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1782352860444360704 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4295537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sitianmei anopenlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis AT tanqingrong anopenlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis AT zhangkerang anopenlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis AT wangyang anopenlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis AT ruiqing anopenlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis AT sitianmei openlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis AT tanqingrong openlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis AT zhangkerang openlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis AT wangyang openlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis AT ruiqing openlabelflexibledosestudyofpaliperidoneextendedreleaseinchinesepatientswithfirstonsetpsychosis |