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新型苯二氮䓬衍生物劳拉西泮治疗焦虑症的安全性和有效性的临床评估。

Clinical assessment of the safety and efficacy of lorazepam, a new benzodiazepine derivative, in the treatment of anxiety.

作者信息

Pinosky D G

出版信息

J Clin Psychiatry. 1978 Oct;39(10 Pt 2):24-9.

PMID:30763
Abstract

In a four-week double-blind study of 68 adult outpatients, lorazepam a new benzodiazepine, administered at an average total daily dosage level of 3.1 mg on a b.i.d. regimen, was clearly superior to placebo in the treatment of neurotic anxiety and its related symptoms. The lorazepam-treated group showed significantly greater improvement than the placebo-treated group (both clinically and statistically), as evidenced by the greater changes on the physician-rated Global Scale as well as by the greater changes in almost all categories on the physician-rated Hamilton Anxiety Scale and the patient-rated Lipman-Rickels 35-Item Self-Rating Scale. There were no clinically significant changes in vital signs or laboratory values and only one side effect, urinary retention (resolved without discontinuing the drug), was reported.

摘要

在一项针对68名成年门诊患者的为期四周的双盲研究中,新型苯二氮䓬类药物劳拉西泮,采用每日两次的给药方案,平均每日总剂量为3.1毫克,在治疗神经性焦虑及其相关症状方面明显优于安慰剂。劳拉西泮治疗组比安慰剂治疗组有显著更大的改善(在临床和统计学上均如此),这体现在医生评定的总体量表上有更大变化,以及医生评定的汉密尔顿焦虑量表和患者评定的利普曼 - 里克斯35项自评量表上几乎所有类别都有更大变化。生命体征或实验室值没有临床显著变化,仅报告了一种副作用,即尿潴留(未停药即缓解)。

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