Suppr超能文献

一项在中国首发精神病患者中进行的帕利哌酮缓释片开放标签、灵活剂量研究。

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

作者信息

Si TianMei, Tan QingRong, Zhang KeRang, Wang Yang, Rui Qing

机构信息

Peking University Institute of Mental Health, Key Laboratory of Mental Health, Ministry of Health (Peking University), Beijing, People's Republic of China.

Fourth Military Medical University, First Hospital, Xi'an, People's Republic of China.

出版信息

Neuropsychiatr Dis Treat. 2015 Jan 6;11:87-95. doi: 10.2147/NDT.S70694. eCollection 2015.

Abstract

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.

摘要

背景

抗精神病药物有助于改善首发精神病患者的精神病性症状。对中国首发精神病患者评估了非典型抗精神病药物帕利哌酮缓释片(pali-ER)的疗效和安全性。

方法

在这项为期8周的开放标签、单臂、多中心研究中,符合《精神疾病诊断与统计手册》第四版标准的首发精神病患者且阳性和阴性症状量表(PANSS)总分≥70的患者,接受灵活剂量的帕利哌酮缓释片(3 - 12毫克/天)治疗。主要疗效终点是从基线到第56天(8周)个人和社会功能(PSP)评分增加≥8分的患者百分比。次要终点包括PANSS总分的降低、临床总体印象严重程度评分的改善、PSP评分、抗精神病药治疗下主观幸福感量表评分,以及未治疗精神病持续时间与PANSS或PSP之间的关系。用治疗中出现的不良事件发生率评估安全性。

结果

总体而言,294例患者中有283例(96%)PSP评分增加≥8分(主要终点,分析集)。对于次要疗效终点,30……此处原文有误,应该是306例患者中有284例(93%)PANSS总分降低≥30%;306例患者中有266例(87%)临床总体印象严重程度量表评分≤3,294例患者中有218例(74%)PSP评分≥71。抗精神病药治疗下主观幸福感量表评分从基线时的平均72.7提高到终点时的94.7。未治疗精神病持续时间与治疗后PSP评分呈负相关,与治疗后PANSS总分呈正相关。最常见的治疗中出现的不良事件是锥体外系症状(12%),以及激越、嗜睡和口干(各4%)。

结论

帕利哌酮缓释片8周灵活剂量(3 - 12毫克/天)治疗使中国首发精神病患者的精神病性症状和社会功能有显著改善,且总体耐受性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5491/4295537/f3f7b38def48/ndt-11-087Fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验