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Quetiapine-Induced Hypomania and its Association with Quetiapine/Norquetiapine Plasma Concentrations: A Case Series of Bipolar Type 2 Patients

机译:喹硫平诱导的轻躁狂及其与喹硫平/去甲平血浆浓度的关联:双相2型患者的病例系列

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摘要

International guidelines consider quetiapine at medium doses (300–400 mg/day) as valid options for the treatment of bipolar depression for the supposed lower risk of a switch to hypomania/mania than antidepressants. Norquetiapine is an active metabolite with antidepressant action. We describe three cases of induced hypomania in bipolar type 2 subjects who received quetiapine extended-release monotherapy (300 mg/day) for a mild/moderate major depressive episode. Quetiapine and norquetiapine plasma concentrations were measured after 1 week of treatment. Hypomania appeared after 7–10 days of quetiapine extended-release monotherapy and all subjects had a quetiapineorquetiapine plasma concentration ratio <1. We propose a ratio value <1 as a predictor of risk for a switch to hypomania in bipolar depressed subjects receiving quetiapine extended-release monotherapy. Future research should ascertain the validity of this laboratory parameter to assess the risk of quetiapine-induced hypomania in large samples of bipolar patients.
机译:国际指南认为,中等剂量(300-400 mg /天)的喹硫平是治疗双相抑郁症的有效选择,因为据信与抗抑郁药相比,转向躁狂症/躁狂症的风险更低。 Norquetiapine是一种具有抗抑郁作用的活性代谢产物。我们描述了在双相2型受试者中接受喹硫平缓释单药治疗(300 mg /天)引起轻度/中度重度抑郁发作的3例躁郁症案例。治疗1周后测量喹硫平和降血平药的血浆浓度。喹硫平缓释单药治疗7-10天后出现低躁狂症,所有受试者的喹硫平/降血平血浆浓度比<1。我们建议比率值<1作为接受喹硫平缓释单药治疗的双相抑郁患者的低躁狂风险的预测指标。未来的研究应确定该实验室参数在评估双相患者大量样本中喹硫平诱发的轻躁狂风险的有效性。

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