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喹硫平:精神分裂症中的剂量-反应关系。

Quetiapine: dose-response relationship in schizophrenia.

作者信息

Sparshatt Anna, Jones Sarah, Taylor David

机构信息

Pharmacy Department, Maudsley Hospital, Denmark Hill, London, England.

出版信息

CNS Drugs. 2008;22(1):49-68; discussion 69-72. doi: 10.2165/00023210-200822010-00004.

Abstract

Quetiapine is a widely used second-generation antipsychotic that is effective in the treatment of schizophrenia and bipolar mania. In recent years, various publications have suggested the possibility that, in some patients, higher than licensed dosages are necessary for full therapeutic effect. A 'high-dose' theory of quetiapine activity has developed, leading many prescribers to disregard the formal upper limit of the quetiapine dosage range (750 or 800 mg/day, depending on local labelling). In this review, we examine the clinical and neuroimaging data relating to the use of quetiapine in acute exacerbations of schizophrenia. Fixed-dose efficacy studies of immediate-release (IR) quetiapine suggest dosages of quetiapine of 150-450 mg/day are more effective than placebo and no less effective than dosages of 600 or 750 mg/day. A fixed-dose study of extended-release quetiapine indicated that dosages of 600 and 800 mg/day were equally efficacious and numerically superior to 400 mg/day. Dosages of IR quetiapine averaging between 254 and 525 mg/day have been shown to be equivalent in efficacy to standard dosages of conventional and other atypical antipsychotics. Pooled data support these findings. Effectiveness studies using quetiapine in daily doses averaging between 565 and 653 mg revealed quetiapine to be somewhat less effective than some comparator drugs. Support for the use of high-dosage quetiapine (>800 mg/day) is very limited: case reports, albeit numerous, describe quetiapine as showing therapeutic effects only at dosages above the licensed range; some data suggest widespread use of higher dosages in practice; and neuroimaging data suggest inadequate dopamine receptor occupancy at standard dosages (although these findings may reflect the low affinity of quetiapine for dopamine receptors). Overall, robust controlled data strongly suggest that the standard dosage range for quetiapine is appropriate for clinical use. The balance of evidence does not support the belief that higher dosages are required for full therapeutic effect, although higher dosage trials are ultimately required to confirm or refute this hypothesis.

摘要

喹硫平是一种广泛使用的第二代抗精神病药物,对治疗精神分裂症和双相躁狂有效。近年来,各种出版物表明,在某些患者中,可能需要高于许可剂量才能达到完全治疗效果。一种“高剂量”的喹硫平活性理论逐渐形成,导致许多开处方者无视喹硫平剂量范围的正式上限(750或800毫克/天,取决于当地标签)。在本综述中,我们研究了与喹硫平用于精神分裂症急性加重期相关的临床和神经影像学数据。速释(IR)喹硫平的固定剂量疗效研究表明,150 - 450毫克/天的喹硫平剂量比安慰剂更有效,且不比600或750毫克/天的剂量效果差。一项缓释喹硫平的固定剂量研究表明,600和800毫克/天的剂量同样有效,且在数值上优于400毫克/天。平均每天254至525毫克的IR喹硫平剂量已被证明在疗效上等同于传统和其他非典型抗精神病药物的标准剂量。汇总数据支持这些发现。使用平均每天565至653毫克剂量的喹硫平的有效性研究表明,喹硫平的效果略逊于一些对照药物。对使用高剂量喹硫平(>800毫克/天)的支持非常有限:尽管有大量病例报告,但这些报告描述喹硫平仅在高于许可范围的剂量下才显示出治疗效果;一些数据表明在实践中广泛使用更高剂量;神经影像学数据表明标准剂量下多巴胺受体占有率不足(尽管这些发现可能反映了喹硫平对多巴胺受体的低亲和力)。总体而言,有力的对照数据强烈表明喹硫平的标准剂量范围适用于临床使用。证据的平衡不支持需要更高剂量才能达到完全治疗效果的观点,尽管最终需要进行更高剂量试验来证实或反驳这一假设。

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