A prospective, multicenter, randomized, parallel-group, open-label study of aripiprazole in the management of patients with schizophrenia or schizoaffective disorder in general psychiatric practice: Broad Effectiveness Trial with Aripiprazole (BETA)

被引:87
作者
Tandon, Rajiv
Marcus, Ronald N.
Stock, Elyse G.
Riera, Linda C.
Kostic, Dusan
Pans, Miranda
McQuade, Robert D.
Nyilas, Margaretta
Iwamoto, Taro
Crandall, David T.
机构
[1] Florida Dept Children & Families, Tallahassee, FL 32399 USA
[2] Bristol Myers Squibb Co, Pharmaceut Res Inst, Wallingford, CT 06492 USA
[3] Bristol Myers Squibb Co, Lawrenceville, NJ USA
[4] Bristol Myers Squibb Co, Braine LAlleud, Belgium
[5] Otsuka Amer Pharmaceut Inc, Princeton, NJ USA
[6] Otsuka Maryland Res Inst Inc, Rockville, MD USA
[7] Bristol Myers Squibb Co, Plainsboro, NJ USA
关键词
aripiprazole; schizophrenia; schizoaffective disorder; outpatient; atypical antipsychotic; clinical trial; RCT; switch study;
D O I
10.1016/j.schres.2005.12.857
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: BETA was designed to evaluate the overall effectiveness of aripiprazole in patients with schizophrenia or schizoaffective disorder treated in a general psychiatry outpatient practice setting. Methods: In this 8-week, multicenter, open-label study, 1599 outpatients with schizophrenia or schizoaffective disorder were randomly assigned to receive either aripiprazole (n = 1295) or another antipsychotic medication (safety control [SC] group; n=304). Aripiprazole was initiated at 15 mg/d with the option to adjust between 10-30 mg/d. The SC medication was specifically selected for each patient by the clinician and dosed according to prescribing guidelines for that medication. The primary effectiveness measure was the Clinical Global Impression-Improvement (CGI-I) score of the aripiprazole group at study end point. Secondary measures included response rates and preference of medicine (POM) ratings by patients and caregivers. Results: Sixty-five percent of aripiprazole patients completed the study. The mean aripiprazole dose at end point was 19.9 mg/d, with approximately 39% of patients starting and remaining at 15 mg/d. At end point, the mean CGI-I score of 2.77 demonstrated that aripiprazole was minimally to moderately effective; the mean CGI-I score for the SC group was 3.59 indicating minimally effective to no change. Fifty-three percent of aripiprazole patients responded to treatment (CGI-I score of I or 2; last-observation-carried-forward [LOCF]), and approximately 71% of patients and caregivers rated aripiprazole as better than the prestudy medication on the POM (LOCF). Incidence and severity of adverse events (AEs) were similar to those reported in double-blind, randomized, placebo-controlled aripiprazole clinical trials. The most frequent AE in the aripiprazole group was insomnia (24%). Conclusions: Aripiprazole was effective for the treatment of schizophrenia and schizoaffective disorder in a general psychiatry outpatient practice setting. Overall, aripiprazole was found to be effective by the treating clinician and well accepted by patients and caregivers over the 8-week treatment course. (c) 2006 Elsevier B.V All rights reserved.
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页码:77 / 89
页数:13
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