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阿立哌唑对急性精神分裂症伴不同程度激越患者的疗效:4项随机、安慰剂对照临床试验的事后分析

Aripiprazole effects in patients with acute schizophrenia experiencing higher or lower agitation: a post hoc analysis of 4 randomized, placebo-controlled clinical trials.

作者信息

Marder Stephen R, West Britt, Lau Gina S, Pultz Joseph A, Pikalov Andrei, Marcus Ronald N, Gutierrez-Esteinou Rolando, Crandall David T

机构信息

Semel Institute of Neuroscience, UCLA, Los Angeles, Calif, USA.

出版信息

J Clin Psychiatry. 2007 May;68(5):662-8. doi: 10.4088/jcp.v68n0503.

Abstract

OBJECTIVE

Patients with acute schizophrenia who are agitated typically manifest worse overall symptomatology and are generally more challenging to treat than nonagitated patients. In order to determine whether baseline agitation level influences treatment response, the effects of oral aripiprazole in acute patients with schizophrenia experiencing either higher or lower levels of agitation were examined.

METHOD

A post hoc analysis of pooled data from the first 4 or 6 weeks of 4 randomized, double-blind, placebo-controlled aripiprazole trials was conducted. Patients with a DSM-IV diagnosis of acute schizophrenia randomly assigned to treatment with either aripiprazole 10, 15, 20, or 30 mg/day (N = 790) or placebo (N = 397) were divided into groups experiencing higher or lower agitation at baseline. Higher agitation was defined as a baseline Positive and Negative Syndrome Scale (PANSS)-Excited Component (PEC) score of > or = 14 and a score of > or = 4 on at least 1 PEC item (excitement, hostility, tension, uncooperativeness, or poor impulse control). Analysis of covariance was used to evaluate PANSS total, Clinical Global Impressions-Improvement scale (CGI-I), and PEC scores between aripiprazole and placebo within the higher and lower agitation groups.

RESULTS

In both the higher and lower agitation groups, aripiprazole treatment produced significantly lower PANSS total, CGI-I, and PEC scores at weeks 2 to 6, compared with placebo (p < .05 for each measure). Percentage of concomitant benzodiazepine use was similar at end point for aripiprazole and placebo, and adverse events were generally mild across groups.

CONCLUSIONS

Aripiprazole significantly improved the core symptoms of acute schizophrenia regardless of baseline agitation level. In particular, agitation symptoms were significantly decreased in patients with higher baseline agitation. Improvements appeared to be independent of benzodiazepine use or excessive sedation effects. These results suggest that oral aripiprazole is an effective and safe treatment option for patients with acute schizophrenia who manifest agitation symptoms.

摘要

目的

急性精神分裂症激越患者通常总体症状更严重,与非激越患者相比,治疗起来通常更具挑战性。为了确定基线激越水平是否会影响治疗反应,研究了口服阿立哌唑对激越水平较高或较低的急性精神分裂症患者的疗效。

方法

对4项阿立哌唑随机、双盲、安慰剂对照试验前4周或6周汇总数据进行事后分析。根据《精神疾病诊断与统计手册》第四版(DSM-IV)诊断为急性精神分裂症的患者,随机分配接受10、15、20或30mg/日阿立哌唑治疗(N = 790)或安慰剂治疗(N = 397),并根据基线激越水平分为较高或较低激越组。较高激越定义为基线阳性和阴性症状量表(PANSS)-激越分量表(PEC)得分≥14分,且至少1项PEC条目(兴奋、敌意、紧张、不合作或冲动控制差)得分≥4分。采用协方差分析评估较高和较低激越组中阿立哌唑与安慰剂之间的PANSS总分、临床总体印象改善量表(CGI-I)和PEC得分。

结果

在较高和较低激越组中,与安慰剂相比,阿立哌唑治疗在第2至6周时PANSS总分、CGI-I和PEC得分均显著降低(每项指标p < 0.05)。阿立哌唑和安慰剂在终点时同时使用苯二氮䓬类药物的比例相似,且各组不良事件总体较轻。

结论

无论基线激越水平如何,阿立哌唑均能显著改善急性精神分裂症的核心症状。特别是,基线激越水平较高的患者激越症状显著减轻。改善似乎与使用苯二氮䓬类药物或过度镇静作用无关。这些结果表明,口服阿立哌唑是治疗有激越症状的急性精神分裂症患者的一种有效且安全的治疗选择。

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