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阿立哌唑治疗的青少年精神分裂症患者阳性和阴性症状量表衍生敌意因子的变化:随机临床试验数据的事后分析

Changes in positive and negative syndrome scale-derived hostility factor in adolescents with schizophrenia treated with aripiprazole: post hoc analysis of randomized clinical trial data.

作者信息

Robb Adelaide S, Carson William H, Nyilas Margaretta, Ali Mirza, Forbes Robert A, Iwamoto Taro, Assunção-Talbott Sheila, Whitehead Richard, Pikalov Andrei

机构信息

Children's National Medical Center, Washington, DC 20010-2970, USA.

出版信息

J Child Adolesc Psychopharmacol. 2010 Feb;20(1):33-8. doi: 10.1089/cap.2008.0163.

Abstract

INTRODUCTION

This post hoc analysis evaluated the effects of aripiprazole on Positive and Negative Syndrome Scale (PANSS) Hostility factor scores in adolescents with schizophrenia.

METHODS

In total, 302 adolescents (13-17 years) with schizophrenia were enrolled in a 6-week, multicenter, double-blind, randomized, placebo-controlled trial comparing aripiprazole (10 or 30 mg/day) with placebo. The PANSS was the primary outcome measure. To determine the effect of aripiprazole on hostility, a post hoc analysis of the PANSS Hostility factor and individual items was performed.

RESULTS

Aripiprazole was superior to placebo in reducing PANSS Hostility factor scores in adolescents with schizophrenia. After 6 weeks, aripiprazole 10 mg/day and aripiprazole 30 mg/day showed a statistically significant improvement versus placebo (-3.0, -3.7, versus -2.1; p < 0.05; last observation carried forward [LOCF]) in the PANSS Hostility factor. For aripiprazole 30 mg/day, statistically significant separation from placebo was evident from week 3 through week 6 and at week 6 for aripiprazole 10 mg/day. Individual PANSS Hostility, Uncooperativeness, and Poor Impulse Control Items showed statistically significant improvement with aripiprazole 30 mg/day over placebo at end point.

CONCLUSIONS

This post hoc analysis shows that aripiprazole (10 and 30 mg/day) is an effective treatment for hostility symptoms in adolescents with schizophrenia. Clinical trials information: ClinicalTrials.gov identifier: NCT00102063.

摘要

引言

本事后分析评估了阿立哌唑对精神分裂症青少年阳性和阴性症状量表(PANSS)敌对因子得分的影响。

方法

总共302名13至17岁的精神分裂症青少年参加了一项为期6周的多中心、双盲、随机、安慰剂对照试验,比较阿立哌唑(10或30毫克/天)与安慰剂。PANSS是主要结局指标。为确定阿立哌唑对敌对情绪的影响,对PANSS敌对因子和各个项目进行了事后分析。

结果

在降低精神分裂症青少年的PANSS敌对因子得分方面,阿立哌唑优于安慰剂。6周后,阿立哌唑10毫克/天和阿立哌唑30毫克/天在PANSS敌对因子方面与安慰剂相比显示出统计学上的显著改善(分别为-3.0、-3.7,而安慰剂为-2.1;p<0.05;末次观察结转[LOCF])。对于阿立哌唑30毫克/天,从第3周直至第6周与安慰剂有统计学上的显著差异,对于阿立哌唑10毫克/天在第6周时与安慰剂有统计学上的显著差异。在终点时,PANSS敌对、不合作和冲动控制不良各个项目与安慰剂相比,阿立哌唑30毫克/天显示出统计学上的显著改善。

结论

本事后分析表明,阿立哌唑(10毫克/天和30毫克/天)是治疗精神分裂症青少年敌对症状的有效药物。临床试验信息:ClinicalTrials.gov标识符:NCT00102063。

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