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首页> 外文期刊>Journal of psychopharmacology >Psychopharmacological treatment of depression, anxiety, irritability and insomnia in patients receiving interferon-alpha: a prospective case series and a discussion of biological mechanisms.
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Psychopharmacological treatment of depression, anxiety, irritability and insomnia in patients receiving interferon-alpha: a prospective case series and a discussion of biological mechanisms.

机译:接受α-干扰素治疗的患者抑郁,焦虑,烦躁和失眠的心理药物治疗:前瞻性病例系列和生物学机制的讨论。

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摘要

We studied 60 patients receiving a 1-year course of interferon (IFN)-alpha therapy for chronic viral hepatitis. Patients underwent psychiatric assessment before starting the IFN-alpha therapy, and monthly throughout the therapy, using the Structured Clinical Interview for the DSM-III-R, the 17-item Hamilton Depression Rating Scale, the Beck Depression Inventory and the Spielberg State and Trait Anxiety Inventory. Five patients had a baseline diagnosis of major depression and 18 (30%) developed an IFN-alpha-induced psychiatric adverse effect; 12 of these 23 patients received psychopharmacological treatment (patients and clinicians jointly decided the need for treatment). Two of the five patients with baseline depression started an antidepressant treatment (paroxetine) together with the IFN-alpha and successfully completed the IFN-alpha therapy. Ten patients received treatment for the IFN-alpha-induced psychiatric adverse effects (depression in five patients, anxiety in two patients, severe irritability in two patients and insomnia in one patient). Depression was treated with paroxetine, amisulpride or levosulpiride; anxiety and insomnia were treated with benzodiazepines; and irritability was treated with thioridazine. Individual response to medications was measured with the Clinical Global Impression scale. Of the patients with IFN-alpha-induced depression, two received paroxetine (one showed a good response), two received amisulpride (one showed a good response) and one did not respond to levosulpiride but responded to paroxetine. The patients experiencing anxiety or insomnia responded well to benzodiazepines. One patient showed a good response, and one a poor response, to thioridazine for irritability. Only one patient interrupted the therapy because of psychiatric adverse effects. Overall, the 12 patients that received psychopharmacological treatment developed less severe psychopathological symptoms during the IFN-alpha therapy compared to the 11 patients who had untreated baseline depression or untreated IFN-alpha-induced psychiatric adverse effects. Thus, psychopharmacological management can successfully treat psychiatric symptoms in patients who are receiving IFN-alpha.
机译:我们研究了60名接受1年疗程的干扰素(IFN)-α治疗慢性病毒性肝炎的患者。患者在开始IFN-α治疗之前和整个治疗过程中每月都要接受精神病学评估,使用DSM-III-R的结构化临床访谈,17个项的汉密尔顿抑郁量表,贝克抑郁量表以及斯皮尔伯格状态和特质焦虑量表。基线诊断为重度抑郁症的患者为5位,其中18位(30%)出现了IFN-α引起的精神病学不良反应;这23名患者中有12名接受了心理药物治疗(患者和临床医生共同决定是否需要治疗)。五名基线抑郁症患者中有两人与IFN-α一起开始了抗抑郁治疗(帕罗西汀),并成功完成了IFN-α的治疗。 10例患者接受了IFN-α引起的精神疾病的不良反应(5例患者抑郁,2例患者焦虑,2例患者烦躁不安和1例失眠)。抑郁症用帕罗西汀,氨磺必利或左旋磺必利治疗;苯二氮卓治疗焦虑和失眠。并用硫代哒嗪治疗易怒。个体对药物的反应用临床总体印象量表进行测量。在IFN-α引起的抑郁症患者中,两名接受帕罗西汀(一个显示出良好的反应),两名接受氨磺必利(一个显示出良好的反应),另一名对左氧舒必利无反应,但对帕罗西汀有反应。焦虑或失眠的患者对苯二氮卓类药物反应良好。一位患者对硫代哒嗪表现出良好的反应,而另一位反应较差,因为有易怒性。只有一名患者由于精神病的不良影响而中断了治疗。总体而言,与未经基线基线抑郁或未经治疗的IFN-α引起的精神病学不良反应的11名患者相比,接受心理药物治疗的12例患者在IFN-α治疗期间出现的严重精神病理症状较轻。因此,心理药物管理可以成功治疗正在接受IFN-α的患者的精神症状。

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