Adjunctive Risperidone for Partially Responsive People with Schizophrenia Treated with Clozapine

被引:36
|
作者
Weiner, Elaine [1 ]
Conley, Robert R. [2 ]
Ball, M. Patricia [1 ]
Feldman, Stephanie [1 ]
Gold, James M. [1 ]
Kelly, Deanna L. [1 ]
Wonodi, Ikwunga [1 ]
McMahon, Robert P. [1 ]
Buchanan, Robert W. [1 ]
机构
[1] Univ Maryland, Sch Med, Dept Psychiat, Maryland Psychiat Res Ctr, Baltimore, MD 21228 USA
[2] Eli Lilly & Co, Lilly Biomed Neurosci, Indianapolis, IN 46285 USA
关键词
schizophrenia; risperidone; clozapine; treatment resistant; positive symptoms; negative symptoms; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; REFRACTORY SCHIZOPHRENIA; ANTIPSYCHOTIC-DRUGS; RECEPTOR OCCUPANCY; CLINICAL-RESPONSE; RATING-SCALE; HALOPERIDOL; AUGMENTATION; TESTS;
D O I
10.1038/npp.2010.101
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The large numbers of partial clozapine responders represent a major therapeutic challenge. Unfortunately, there are no clear data to support how best to treat these patients. This study examines the efficacy and safety of adjunctive risperidone in a well-defined treatment-resistant population optimally treated with clozapine. A total of 69 inpatients and outpatients with DSM-IV schizophrenia or schizoaffective disorder entered a 16-week double-blind, placebo-controlled, randomized clinical trial. Of them, 33 participants were randomized to risperidone and 36 were randomized to placebo. There was no significant group difference in the predefined response criteria. There were modest group differences for Brief Psychiatric Rating Scale (BPRS) positive symptoms, which were significant in the completer analysis (F = 5.70; df = 1, 70.3; p = 0.02; ES = 0.27) but not the intent-to-treat (ITT) analyses (F = 3.01; df = 1, 77.5; p = 0.09; ES = 0.19). A similar pattern was found for the BPRS total score, with the completer analysis showing a significant improvement in the risperidone group (F = 5.21; df = 1, 64.9; p = 0.03; ES = 0.27), whereas the ITT analysis was not significant (F = 3.52; df = 1, 71.3; p = 0.06; ES = 0.22). In addition, there was a small, but significant, group difference for negative symptoms, as measured by the SANS total score, which favored the risperidone group (F = 5.67; df = 1, 78.7; p = 0.02; ES = 0.24). There were no significant group differences on safety measures, including neuropsychological test and extrapyramidal symptom scores. A significant elevation of prolactin in the risperidone group was observed. The study results suggest that adjunctive risperidone may have a modest benefit for treatment-resistant clozapine patients. The study results are discussed in the context of previous double-blind studies of adjunctive risperidone. (clinicaltrials.gov, trial number: NCT00056498). Neuropsychopharmacology (2010) 35, 2274-2283; doi:10.1038/npp.2010.101; published online 21 July 2010
引用
收藏
页码:2274 / 2283
页数:10
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