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美国曲唑酮治疗临床抑郁症对照试验综述。

Overview of USA controlled trials of trazodone in clinical depression.

作者信息

Feighner J P, Boyer W F

机构信息

Feighner Research Institute, Encinitas, CA.

出版信息

Psychopharmacology (Berl). 1988;95 Suppl:S50-3. doi: 10.1007/BF00172631.

Abstract

Trazodone's unique chemical structure reflects its distinct pharmacologic profile. Its antidepressant efficacy is postulated to occur through serotonin reuptake inhibition. It has little effect on other neurotransmitter systems. In the United States it has been studied in several double-blind trials which compared it to standard antidepressants and placebo. Both in- and outpatients spanning a spectrum of age and diagnoses have been studied. Trazodone has been shown to be at least as effective as standard antidepressants. There are few anticholinergic or cardiovascular side effects. Adverse reactions include drowsiness, dizziness, headache, nausea and rarely, priapism. It is relatively safe in overdose. Trazodone deserves special consideration in the treatment of patients with depression accompanied by marked agitation, anxiety, and insomnia, as well as those unable to tolerate anticholinergic side effects.

摘要

曲唑酮独特的化学结构反映了其独特的药理学特性。据推测,其抗抑郁疗效是通过抑制5-羟色胺再摄取实现的。它对其他神经递质系统影响很小。在美国,已经进行了多项双盲试验,将其与标准抗抑郁药和安慰剂进行比较。研究对象包括不同年龄和诊断的门诊和住院患者。结果表明,曲唑酮至少与标准抗抑郁药一样有效。几乎没有抗胆碱能或心血管副作用。不良反应包括嗜睡、头晕、头痛、恶心,很少出现阴茎异常勃起。过量服用时相对安全。对于伴有明显激越、焦虑和失眠的抑郁症患者,以及无法耐受抗胆碱能副作用的患者,曲唑酮在治疗中值得特别考虑。

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