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增效氯氮平合用曲司氯铵:一项双盲、随机、安慰剂对照研究。

Augmenting clozapine with sertindole: a double-blind, randomized, placebo-controlled study.

机构信息

Unit for Psychiatric Research, Aalborg Psychiatric Hospital, Aarhus University Hospital, Aalborg, Denmark.

出版信息

J Clin Psychopharmacol. 2012 Apr;32(2):173-8. doi: 10.1097/JCP.0b013e318248dfb8.

Abstract

Clozapine augmentation with antipsychotic drugs is widely used despite sparse evidence supporting this strategy. Sertindole is a nonsedating atypical antipsychotic drug with low affinity for cholinergic receptors, which makes it potentially suitable for augmentation of clozapine. The study design was a 12-week, double-blind, randomized, placebo-controlled study including patients with International Statistical Classification of Diseases, 10th Revision schizophrenia (F20.0-F20.3) and treated with clozapine for at least 6 months who had not achieved sufficient response. Patients were randomized 1:1 to either sertindole 16 mg or placebo, and assessment was done at baseline and after 6 and 12 weeks. Assessment included the Positive and Negative Syndrome Scale, Clinical Global Impression, Udvalg for Kliniske Undersøgelser, World Health Organization Quality of Life Brief, Drug Attitude Inventory, fasting glucose, lipids, and electrocardiogram. Clozapine augmentation with sertindole was not superior to placebo regarding total score or subscale score of the Positive and Negative Syndrome Scale, Clinical Global Impression, World Health Organization Quality of Life Brief, or Drug Attitude Inventory. No increased adverse effects compared with placebo were found. Four patients randomized to sertindole experienced a significant worsening of psychosis, and 2 of them required psychiatric admission. Metabolic parameters were unchanged during the study, but augmentation of clozapine with sertindole was associated with a 12-millisecond (SD, 20-millisecond) QTc prolongation compared with 0 millisecond (SD, 20 milliseconds) in the placebo group (P < 0.03). Augmentation with sertindole showed no benefits compared with placebo. Psychiatrists should be aware that augmentation might not add any benefits for the patients and in some cases worsen psychosis.

摘要

氯氮平增效治疗联合使用抗精神病药物尽管证据稀少,但仍被广泛应用。曲唑酮是非镇静性的非典型抗精神病药物,对胆碱能受体的亲和力低,使其可能适合作为氯氮平的增效剂。研究设计为 12 周、双盲、随机、安慰剂对照研究,纳入患有国际疾病分类第 10 版精神分裂症(F20.0-F20.3)的患者,这些患者接受氯氮平治疗至少 6 个月,但未获得充分疗效。患者以 1:1 的比例随机分为曲唑酮 16 mg 组或安慰剂组,在基线和 6 周、12 周时进行评估。评估包括阳性和阴性症状量表、临床总体印象、Udvalg for Kliniske Undersøgelser、世界卫生组织生活质量简表、药物态度量表、空腹血糖、血脂和心电图。与安慰剂相比,曲唑酮增效氯氮平在阳性和阴性症状量表、临床总体印象、世界卫生组织生活质量简表或药物态度量表的总分或子量表评分方面均不占优势。与安慰剂相比,未发现不良反应增加。随机分配至曲唑酮组的 4 例患者精神病恶化显著,其中 2 例需要住院治疗。研究期间代谢参数无变化,但与安慰剂组相比,曲唑酮增效氯氮平可导致 QTc 延长 12 毫秒(标准差,20 毫秒),而安慰剂组则为 0 毫秒(标准差,20 毫秒)(P < 0.03)。与安慰剂相比,曲唑酮增效无明显获益。精神科医生应意识到增效可能对患者无益,且在某些情况下会恶化精神病。

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