非典型抗精神病药物治疗失眠症的说明书外使用

Anna K. Morin
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引用次数: 4

摘要

尽管支持证据有限,非典型或第二代抗精神病药物(特别是奥氮平、喹硫平和利培酮)的说明书外使用并不罕见。这些药物的说明书外使用治疗失眠是本综述的重点。虽然与典型或第一代抗精神病药物相比,非典型抗精神病药物与迟发性运动障碍、锥体外系副作用的风险较低有关,并且对精神分裂症患者的认知缺陷和阴性症状有更有利的作用,但它们并非没有风险。非典型抗精神病药物的代谢不良反应尤其成问题,即使剂量低于用于治疗fda批准适应症的剂量。大多数非典型抗精神病药物的受体亲和力谱促进镇静。h1 -组胺受体阻断水平被认为与嗜睡和镇静最相关。一些研究评价了非典型抗精神病药物喹硫平的安全性和有效性。
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Off-label use of atypical antipsychotic agents for treatment of insomnia
Despite limited supporting evidence, off-label uses of atypical or second generation antipsychotics (particularly olanzapine, quetiapine, and risperidone) are not uncommon. The off-label use of these agents for the treatment of insomnia is the focus of this review. While atypical antipsychotics are associated with a lower risk of tardive dyskinesia, extrapyramidal side effects, and more favorable effects on cognitive deficits and negative symptomatology in schizophrenic patients compared to typical or first generation antipsychotic agents, they are not without risks. Metabolic adverse effects are particularly problematic with atypical antipsychotics, even at doses lower than those used to treat FDA-approved indications. The receptor affinity profiles of most atypical antipsychotic agents promote sedation. The level of H1-histamine receptor blockade is believed to be most associated with somnolence and sedation. Several studies evaluating the safety and efficacy of the atypical antipsychotics quetiapine, o...
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