Clozapine alone versus clozapine and risperidone with refractory schizophrenia

被引:192
|
作者
Honer, WG
Thornton, AE
Chen, EYH
Chan, RCK
Wong, JOY
Bergmann, A
Falkai, P
Pomarol-Clotet, E
McKenna, PJ
Stip, E
Williams, R
MacEwan, GW
Wasan, K
Procyshyn, R
Leung, SP
Wong, JOY
Rodriguez, JP
Lalonde, P
Stip, E
Pomarol-Clotet, E
McKenna, PJ
MacEwan, GW
Chen, EYH
Chan, RCK
Flynn, SW
Altman, S
Honer, WG
Thornton, AE
Procyshyn, R
Huckin, S
Au, T
Boudreau, A
Humphries, B
Williams, R
Wasan, K
Bergmann, A
Falkai, P
Wobrock, T
Wollny, H
机构
[1] Univ British Columbia, Dept Psychiat, Vancouver, BC, Canada
[2] Univ British Columbia, Div Pharmaceut & Biopharmaceut, Vancouver, BC, Canada
[3] Simon Fraser Univ, Dept Psychol, Burnaby, BC V5A 1S6, Canada
[4] Univ Hong Kong, Dept Psychiat, Hong Kong, Hong Kong, Peoples R China
[5] Sun Yat Sen Univ, Dept Psychol, Guangzhou, Peoples R China
[6] Castle Peak Hosp, Hong Kong, Hong Kong, Peoples R China
[7] Univ Saarland, Dept Psychiat, D-6650 Homburg, Germany
[8] Univ Cambridge, Dept Psychiat, Cambridge, England
[9] Univ Montreal, Dept Psychiat, Montreal, PQ H3C 3J7, Canada
[10] Riverview Hosp, Port Coquitlam, BC, Canada
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2006年 / 354卷 / 05期
关键词
D O I
10.1056/NEJMoa053222
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: The treatment of schizophrenia with multiple antipsychotic drugs is common, but the benefits and risks are not known. METHODS: In a randomized, double-blind study, we evaluated patients with schizophrenia and a poor response to treatment with clozapine. The patients continued to take clozapine and were randomly assigned to receive eight weeks of daily augmentation with 3 mg of risperidone or with placebo. This course of treatment was followed by an optional 18 weeks of augmentation with risperidone. The primary outcome was reduction in the total score for severity of symptoms on the Positive and Negative Syndrome Scale (PANSS). The secondary outcomes included cognitive functioning. RESULTS: A total of 68 patients were randomly assigned to treatment. In the double-blind phase, the mean total score for the severity of symptoms decreased from baseline to eight weeks in both the risperidone and the placebo groups. There was no statistically significant difference in symptomatic benefit between augmentation with risperidone and placebo: 9 of 34 patients receiving placebo and 6 of 34 receiving risperidone responded to treatment (P=0.38). The mean difference in the change in PANSS scores from baseline to eight weeks between those receiving risperidone and those receiving placebo was 0.1 (95 percent confidence interval, -7.3 to 7.0). The verbal working-memory index showed a small decline in the risperidone group and a small improvement in the placebo group (P=0.02 for the comparison between the two groups in the change from baseline). The increase in fasting blood glucose levels was mildly greater in the risperidone group than in the placebo group (16.2 vs. 1.8 mg per deciliter [0.90 vs. 0.10 mmol per liter], P=0.04). The incidence and severity of other side effects did not differ between the two groups. CONCLUSIONS: In this short-term study, the addition of risperidone to clozapine did not improve symptoms in patients with severe schizophrenia.
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收藏
页码:472 / 482
页数:11
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