Quetiapine treatment of psychosis associated with dementia: A double-blind, randomized, placebo-controlled clinical trial

被引:104
|
作者
Tariot, Pierre N.
Schneider, Lon
Katz, Ira R.
Mintzer, Jacobo E.
Street, Jamie
Copenhaver, Margaret
Williams-Hughes, Celeste
机构
[1] Banner Alzheimers Dis Inst, Memory Disorders Ctr, Phoenix, AZ 85006 USA
[2] Univ So Calif, Keck Sch Med, Dept Psychiat, Los Angeles, CA USA
[3] Univ Penn, Sect Geriatr Psychiat, Philadelphia, PA 19104 USA
[4] Med Univ S Carolina, Inst Psychiat, Charleston, SC 29425 USA
[5] AstraZeneca Pharmaceut LP, Wilmington, DE USA
[6] Biostat Consultant, New Hope, PA USA
来源
关键词
Alzheimer disease; elderly; haloperidol; quetiapine;
D O I
10.1097/01.JGP.0000196628.12010.35
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objectives: The objectives of this study were to evaluate the efficacy, safety, and tolerability of quetiapine for treating psychosis in patients with probable/possible Alzheimer disease and assess its impact on other psychopathology and social and daily functioning. Method: The authors conducted a multicenter, double-blind, placebo-controlled, randomized trial of flexibly dosed quetiapine and haloperidol. Primary outcomes were change in total Brief Psychiatric Rating Scale (BPRS) and Clinical Global Impressions -Severity of Illness (CGI-S) scores at week 10. Secondary outcomes included BPRS factors, Neuropsychiatric Inventory (NPI), Multidimensional Observation Scale for Elderly Subjects (MOSES), and Physical Self-Maintenance Scale (PSMS). Results: Two hundred eighty-four participants (mean age: 83.2 years) were randomized; 63.4% completed; and mean Mini-Mental State Examination score was 12.8. Median of the mean daily dose was 96.9 mg for quetiapine and 1.9 mg for haloperidol. No differential benefit was seen on any psychosis measure. BPRS agitation factor scores improved with quetiapine versus placebo and not quetiapine versus haloperidol. BPRS anergia scores worsened with haloperidol versus quetiapine but not quetiapine versus placebo. No NPI factors showed change, including the agitation factor. MOSES Withdrawal Subscale and PSMS total scores worsened with haloperidol versus quetiapine. Somnolence occurred in 25.3%, 36.2%, and 4.1% of the quetiapine, haloperidol, and placebo groups, respectively; parkinsonism was most prevalent in the haloperidol group; other safety and tolerability measures differed little among groups. Conclusion: All treatment groups showed improvement in measures of psychosis without significant differences between them when planned comparisons were performed. Participants treated with quetiapine or haloperidol showed inconsistent evidence of improvement in agitation. Tolerability was better with quetiapine compared with haloperidol.
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收藏
页码:767 / 776
页数:10
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