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文拉法辛缓释胶囊治疗惊恐障碍:灵活剂量、双盲、安慰剂对照研究。

Venlafaxine extended-release capsules in panic disorder: flexible-dose, double-blind, placebo-controlled study.

作者信息

Bradwejn Jacques, Ahokas Antti, Stein Dan J, Salinas Eliseo, Emilien Gerard, Whitaker Timothy

机构信息

University of Ottawa Institute of Mental Health Research, Royal Ottawa Hospital, 1145 Carling Avenue, Ottawa, Ontario, Canada K1Z 7K4.

出版信息

Br J Psychiatry. 2005 Oct;187:352-9. doi: 10.1192/bjp.187.4.352.

Abstract

BACKGROUND

Venlafaxine extended-release (ER) has proven efficacy in the treatment of anxiety symptoms in major depression, generalised anxiety disorder and social anxiety disorder.

AIMS

To evaluate the efficacy, safety and tolerability of venlafaxine ER in treating panic disorder.

METHOD

Adult out-patients (n=361) with panic disorder were randomly assigned to receive venlafaxine ER (75-225 mg/day) or placebo for up to 10 weeks in a double-blind study.

RESULTS

Venlafaxine ER was not associated with a greater proportion of patients free from full-symptom panic attacks at the final on-therapy evaluation, but was associated with lower mean panic attack frequency and a higher proportion free from limited-symptom panic attacks, higher response and remission rates, and improvements in anticipatory anxiety, fear and avoidance. Adverse events were comparable with those of the drug in depression and anxiety disorders.

CONCLUSIONS

Venlafaxine ER seems to be effective and well tolerated in the short-term treatment of panic disorder.

摘要

背景

文拉法辛缓释剂已被证明在治疗重度抑郁症、广泛性焦虑症和社交焦虑症的焦虑症状方面有效。

目的

评估文拉法辛缓释剂治疗惊恐障碍的疗效、安全性和耐受性。

方法

在一项双盲研究中,将361名患有惊恐障碍的成年门诊患者随机分配接受文拉法辛缓释剂(75 - 225毫克/天)或安慰剂治疗,为期10周。

结果

在最终治疗评估时,接受文拉法辛缓释剂治疗的患者中完全没有症状性惊恐发作的比例并不更高,但与较低的平均惊恐发作频率、较高比例的无有限症状惊恐发作、较高的有效率和缓解率以及预期焦虑、恐惧和回避症状的改善有关。不良事件与该药在抑郁症和焦虑症中的情况相当。

结论

文拉法辛缓释剂在惊恐障碍的短期治疗中似乎有效且耐受性良好。

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