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每日一次的文拉法辛缓释剂(XR)治疗门诊抑郁症患者焦虑症状的疗效。

Efficacy of once-daily venlafaxine extended release (XR) for symptoms of anxiety in depressed outpatients.

作者信息

Feighner J P, Entsuah A R, McPherson M K

机构信息

Feighner Research Institute, San Diego, CA 92121, USA.

出版信息

J Affect Disord. 1998 Jan;47(1-3):55-62. doi: 10.1016/s0165-0327(97)00109-2.

Abstract

The effects of once-daily venlafaxine extended release (XR) 75-225 mg/day on symptoms of anxiety in depressed outpatients were assessed in two randomized, double-blind, placebo-controlled trials. In study 1, venlafaxine XR was significantly (p < or = 0.05) more effective than placebo by week 4 in relieving anxiety symptoms among patients with moderate or greater anxiety (anxiety-psychic item score > or = 2) at baseline. Among patients with severe (anxiety-psychic item score > or = 3) anxiety, venlafaxine XR was significantly (p < or = 0.05) more effective than placebo beginning at week 6. In study 2, among patients with moderate or greater anxiety (score > or = 2) at baseline, a significant reduction (p < or = 0.05- < or = 0.001) in HAM-D anxiety-psychic item scores was noted with venlafaxine XR compared with placebo from weeks 1 to 8. Among patients with severe anxiety (score > or = 3) at baseline, venlafaxine XR produced a significant reduction (p < or = 0.05- < or = 0.001) in the anxiety-psychic item score compared with placebo from weeks 1 to 8. Discontinuation for adverse events occurred in 11% of patients on venlafaxine XR, and the most common adverse events were nausea, dizziness, insomnia, somnolence and dry mouth. These results indicate that once-daily venlafaxine XR is effective for the treatment of anxiety symptoms associated with major depression in doses ranging from 75 to 225 mg/day.

摘要

在两项随机、双盲、安慰剂对照试验中,评估了每日一次服用文拉法辛缓释剂(XR)75 - 225毫克/天对抑郁症门诊患者焦虑症状的影响。在研究1中,到第4周时,对于基线时中度或更严重焦虑(焦虑 - 精神项目评分≥2)的患者,文拉法辛XR在缓解焦虑症状方面显著(p≤0.05)优于安慰剂。对于严重焦虑(焦虑 - 精神项目评分≥3)的患者,从第6周开始,文拉法辛XR显著(p≤0.05)优于安慰剂。在研究2中,对于基线时中度或更严重焦虑(评分≥2)的患者,与安慰剂相比,从第1周到第8周,文拉法辛XR使汉密尔顿抑郁量表(HAM - D)焦虑 - 精神项目评分显著降低(p≤0.05 - ≤0.001)。对于基线时严重焦虑(评分≥3)的患者,从第1周到第8周,与安慰剂相比,文拉法辛XR使焦虑 - 精神项目评分显著降低(p≤0.05 - ≤0.001)。服用文拉法辛XR的患者中有11%因不良事件停药,最常见的不良事件是恶心、头晕、失眠、嗜睡和口干。这些结果表明,每日一次服用75至225毫克/天文拉法辛XR对治疗与重度抑郁症相关的焦虑症状有效。

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