Calming versus sedative effects of intramuscular olanzapine in agitated patients

被引:84
作者
Battaglia, J
Lindborg, SR
Alaka, K
Meehan, K
Wright, P
机构
[1] Eli Lilly & Co, Lilly Res Labs, Lilly Corp Ctr, Indianapolis, IN 46285 USA
[2] Univ Wisconsin, Sch Med, Madison, WI USA
[3] Maudsley Hosp & Inst Psychiat, London SE5 8AZ, England
[4] Univ London, Inst Psychiat, London, England
[5] Eli Lilly & Co Ltd, Lilly Res Ctr, Surrey, England
关键词
sedation; agitation; intramuscular; olanzapine; schizophrenia; bipolar mania; dementia;
D O I
10.1016/S0735-6757(02)42249-8
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Distinct calming rather than nonspecific sedation is desirable for the treatment of acute agitation. In 3 double-blind studies, acutely agitated patients with schizophrenia (N = 311), bipolar mania (N = 201), or dementia (N = 206) were treated with intramuscular (1-3 injections/24 hrs) olanzapine (2.5-10.0 mg), haloperidol (7.5 mg), lorazepam (2.0 mg), or placebo. The Agitation-Calmness Evaluation Scale (ACES; Eli Lilly and Co.) and treatment-emergent adverse events assessed sedation. Across all studies, 1 patient (lorazepam-treated, bipolar) became unarousable. There were no significant between-group differences in ACES scores of deep sleep or unarousable at any time across. Excluding asleep patients, agitation remained significantly more reduced with olanzapine than placebo (P < .05). The incidences of adverse events indicative of sedation were not significantly different with olanzapine versus comparators. For the treatment of acute agitation associated with schizophrenia, bipolar mania, or dementia, intramuscular olanzapine-treated patients experienced no more sedation than haloperidol- or lorazepam-treated patients and experienced distinct calming rather than nonspecific sedation. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:192 / 198
页数:7
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