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阿立哌唑治疗患有阿尔茨海默病痴呆的机构化患者的精神病:三种固定剂量的多中心、随机、双盲、安慰剂对照评估

Aripiprazole for the treatment of psychoses in institutionalized patients with Alzheimer dementia: a multicenter, randomized, double-blind, placebo-controlled assessment of three fixed doses.

作者信息

Mintzer Jacobo E, Tune Larry E, Breder Christopher D, Swanink René, Marcus Ronald N, McQuade Robert D, Forbes Andy

机构信息

Alzheimer's Research & Clinical Programs, Medical University of South Carolina, North Charleston, SC 29406-6076, USA.

出版信息

Am J Geriatr Psychiatry. 2007 Nov;15(11):918-31. doi: 10.1097/JGP.0b013e3181557b47.

Abstract

OBJECTIVE

To assess the efficacy and safety of aripiprazole for psychosis associated with Alzheimer dementia (AD).

METHODS

In this double-blind, multicenter study, 487 institutionalized patients with psychosis associated with AD were randomized to placebo or aripiprazole, 2, 5 or 10 mg/day. Primary efficacy assessment was the mean change from baseline to week 10 on the Neuropsychiatric Inventory-Nursing Home (NPI-NH) version Psychosis Subscale score. Secondary measures included NPI-NH Total, Clinical Global Impression-Severity of Illness (CGI-S), Brief Psychiatric Rating Scale (BPRS) Core and Total, and the Cohen-Mansfield Agitation Inventory (CMAI) scores.

RESULTS

Aripiprazole 10 mg/day showed significantly greater improvements (mean change [2 x SD]) than placebo on the NPI-NH Psychosis Subscale (-6.87 [8.6] versus -5.13 [10.0]; F = 6.29, df = 1, 422, p = 0.013 by analysis of covariance [ANCOVA]); CGI-S (-0.72 [1.8] versus -0.46 [1.6]; F = 4.68, df = 1, 419, p = 0.031 [ANCOVA]); BPRS Total (-7.12 [18.4] versus -4.17 [21.6]; F = 4.72, df = 1, 399, p = 0.030 [ANCOVA]); BPRS Core (-3.07 [6.9] versus -1.74 [7.8]; F = 7.30, df = 1, 407, p = 0.007 [ANCOVA]); CMAI (-10.96 [22.6] versus -6.64 [28.6]; F = 5.23, df = 1, 410, p = 0.023 [ANCOVA]), and NPI-NH Psychosis response rate (65 versus 50%; chi(2) = 5.52, df = 1, p = 0.019 [CMH]). Aripiprazole 5 mg/day showed significant improvements versus placebo on BPRS and CMAI scores. Aripiprazole 2 mg/day was not efficacious. Cerebrovascular adverse events were reported: aripiprazole 2 mg/day, N = 1; 5 mg/day, N = 2; 10 mg/day, N = 4; placebo, N = 0. No deaths in any group (aripiprazole 2 mg/day, 3%; 5 mg/day, 2%; 10 mg/day, 7%; placebo, 3%) were considered to be treatment-related.

CONCLUSION

Aripiprazole 10 mg/day was efficacious and safe for psychosis associated with AD, significantly improving psychotic symptoms, agitation, and clinical global impression. However, clinicians should be aware of the safety considerations of atypical antipsychotic uses in this population.

摘要

目的

评估阿立哌唑治疗阿尔茨海默病(AD)相关精神病的疗效和安全性。

方法

在这项双盲、多中心研究中,487例患有AD相关精神病的机构化患者被随机分为安慰剂组或阿立哌唑组,剂量为2、5或10mg/天。主要疗效评估指标是从基线到第10周,神经精神科问卷-疗养院版(NPI-NH)精神病分量表评分的平均变化。次要指标包括NPI-NH总分、临床总体印象-疾病严重程度(CGI-S)、简明精神病评定量表(BPRS)核心项目和总分以及科恩-曼斯菲尔德激越量表(CMAI)评分。

结果

阿立哌唑10mg/天在NPI-NH精神病分量表上显示出比安慰剂显著更大的改善(平均变化[2×标准差])(-6.87[8.6]对-5.13[10.0];通过协方差分析[ANCOVA],F=6.29,自由度=1,422,p=0.013);CGI-S(-0.72[1.8]对-0.46[1.6];F=4.68,自由度=1,419,p=0.031[ANCOVA]);BPRS总分(-7.12[18.4]对-4.17[21.6];F=4.72,自由度=1,399,p=0.030[ANCOVA]);BPRS核心项目(-3.07[6.9]对-1.74[7.8];F=7.30,自由度=1,407,p=0.007[ANCOVA]);CMAI(-10.96[22.6]对-6.64[28.6];F=5.23,自由度=1,410,p=0.023[ANCOVA]),以及NPI-NH精神病反应率(65%对50%;卡方=5.52,自由度=1,p=0.019[CMH])。阿立哌唑5mg/天在BPRS和CMAI评分上显示出比安慰剂显著改善。阿立哌唑2mg/天无效。报告了脑血管不良事件:阿立哌唑2mg/天,N=1;5mg/天,N=2;

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