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帕利哌酮缓释片对泰国精神分裂症患者敌意情绪的影响。

Effects of paliperidone extended release on hostility among Thai patients with schizophrenia.

作者信息

Jariyavilas Apichat, Thavichachart Nuntika, Kongsakon Ronnachai, Chantakarn Sunanta, Arunpongpaisal Suwanna, Chantarasak Vasu, Jaroensook Piyadit, Kittiwattanagul Khanogwan, Nerapusee Osot

机构信息

Srithanya Hospital, Department of Mental Health, Ministry of Public Health, Bangkok.

Department of Psychiatry, Faculty of Medicine, Chulalongkorn University, Bangkok.

出版信息

Neuropsychiatr Dis Treat. 2017 Jan 12;13:141-146. doi: 10.2147/NDT.S112063. eCollection 2017.

Abstract

OBJECTIVE

This open-label prospective study investigated the effects of paliperidone extended release (ER) on hostility in Thai patients with schizophrenia.

BACKGROUND

Patients diagnosed with schizophrenia may be hostile or exhibit aggressive behavior, which can occasion their admission to psychiatric hospital. Antipsychotic medications are often used to treat hostility and aggression in such patients. Paliperidone ER is effective and well tolerated in the treatment of schizophrenia. However, there are no data available for paliperidone ER with regard to its efficacy on hostility and aggression among Thai patients. This study was a part of the PERFEcT study, a 6-month, open-label, multicenter, multicountry, prospective trial to explore the safety, efficacy, and functionality of paliperidone ER tablets. The current study included only the data obtained from Thai participants.

MATERIALS AND METHODS

Flexible dosing of paliperidone ER in a range of 3-12 mg/day was used, allowing investigators to adjust the dosage of each subject individually. The 199 Thai patients had a stable Clinical Global Impression - severity score before enrollment. Demographic data were collected at enrollment, and assessments took place at 1, 2, 3, and 6 months postbaseline. The Positive and Negative Syndrome Scale (PANSS) and Personal and Social Performance (PSP) scale were used to evaluate efficacy. In this analysis, we report the findings for the specific PANSS factor P7 (hostility) and the PSP subscale disturbing and aggressive behavior. Data were analyzed using paired -test method to investigate changes in mean PANSS and PSP total and subscale scores. The significance level was set at <0.05.

RESULTS

From a total of 199 Thai patients, 148 patients (74.4%) participated in all visits. There was a significant reduction in mean scores for all total PANSS measures from 1 month onward compared with baseline, as well as ongoing significant reductions in scores from visit to visit. There was a significant reduction in mean hostility score at 2 months (<0.05), 3 months (<0.05), and 6 months (<0.01) (n=148). For the PSP scale, there was a significant across-the-board reduction of mean scores from 3 months onward, including in the disturbing and aggressive behavior subscale (<0.001) (n=148).

CONCLUSION

Switching from previously unsuccessful antipsychotic treatments to paliperidone ER may be a useful option to reduce hostility and disturbing behavior in patients with schizophrenia. This study in Thai patients is in line with findings in other countries and cultures concerning the management of hostility in patients with schizophrenia.

摘要

目的

这项开放标签的前瞻性研究调查了帕利哌酮缓释片(ER)对泰国精神分裂症患者敌意情绪的影响。

背景

被诊断为精神分裂症的患者可能具有敌意或表现出攻击行为,这可能导致他们入住精神病院。抗精神病药物常用于治疗此类患者的敌意和攻击行为。帕利哌酮ER在精神分裂症治疗中有效且耐受性良好。然而,关于帕利哌酮ER对泰国患者敌意和攻击行为的疗效尚无可用数据。本研究是PERFEcT研究的一部分,这是一项为期6个月的开放标签、多中心、多国前瞻性试验,旨在探索帕利哌酮ER片的安全性、疗效和功能。本研究仅纳入了泰国参与者的数据。

材料与方法

采用3 - 12毫克/天范围内的灵活剂量给予帕利哌酮ER,允许研究人员对每个受试者的剂量进行个体化调整。199名泰国患者在入组前临床总体印象 - 严重程度评分稳定。在入组时收集人口统计学数据,并在基线后1、2、3和6个月进行评估。使用阳性和阴性症状量表(PANSS)及个人和社会功能量表(PSP)评估疗效。在本分析中,我们报告特定PANSS因子P7(敌意)以及PSP分量表中干扰和攻击行为的研究结果。使用配对检验方法分析数据,以研究PANSS和PSP总分及分量表分数的变化。显著性水平设定为<0.05。

结果

在总共199名泰国患者中,148名患者(74.4%)参加了所有访视。与基线相比,从第1个月起所有PANSS总分测量的平均分显著降低,并且每次访视时分数持续显著降低。在第2个月(<0.05)、第3个月(<0.05)和第6个月(<0.01)时,平均敌意得分显著降低(n = 148)。对于PSP量表,从第3个月起平均分全面显著降低,包括干扰和攻击行为分量表(<0.001)(n = 148)。

结论

从先前未成功的抗精神病治疗转换为帕利哌酮ER可能是减少精神分裂症患者敌意和干扰行为的一个有用选择。这项针对泰国患者的研究与其他国家和文化中关于精神分裂症患者敌意管理的研究结果一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1027/5238754/1187440db156/ndt-13-141Fig1.jpg

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