奎硫平XR治疗抑郁症和焦虑症的随机、安慰剂对照疗效研究。

Nisha Ravindran, Martha McKay, Angela Paric, Sunny Johnson, Ranjith Chandrasena, Gaby Abraham, Arun V Ravindran
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引用次数: 2

摘要

目的:喹硫平被批准作为重度抑郁症(MDD)的辅助治疗和双相抑郁症的单药治疗。它经常在标签外用于治疗焦虑状况和作为治疗难治性抑郁症的增强剂。然而,它对伴发焦虑症的抑郁症的益处尚未得到系统的评估。目前的研究评估了喹硫平作为治疗重度抑郁症合并焦虑症的一线抗抑郁药物的增强剂的益处和耐受性。方法:在这项多中心试验(2008年6月- 2013年6月)中,76名原发性诊断为单相抑郁症合并至少一种焦虑症的成年人(年龄18-65岁)(根据DSM-IV-TR标准)以2:1的比例接受灵活剂量喹硫平缓释片(XR) 50- 300mg /d或安慰剂作为12周的附加治疗。评估抑郁、焦虑、生活满意度和不良事件。结果:两组患者抑郁、焦虑、功能均有明显改善。在主要结局指标上,喹硫平在改善抑郁方面优于安慰剂(17项汉密尔顿抑郁评定量表评分:平均差异= -3.64;95% CI, -7.01至-0.27)和焦虑症状(汉密尔顿焦虑评定量表评分:平均差异= -4.02;95% CI, -7.41至-0.64),以及临床总体印象-疾病严重程度量表评分(平均差异= -0.64;95% CI, -1.13至-0.15)。在Montgomery-Asberg抑郁评定量表、Beck抑郁量表、宾夕法尼亚州立大学焦虑问卷和生活质量满意度和享受问卷等次要测量中,喹硫平比安慰剂有更大程度的改善,但组间差异无统计学意义。喹硫平耐受性良好,大多数不良反应轻微,无严重不良反应。结论:喹硫平强化治疗可能是一种有效的干预重度抑郁症伴发焦虑的方法。试验注册:ClinicalTrials.gov标识符:NCT00688818。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Randomized, Placebo-Controlled Effectiveness Study of Quetiapine XR in Comorbid Depressive and Anxiety Disorders.

Objective: Quetiapine is approved as an adjunctive treatment for major depressive disorder (MDD) and as monotherapy for bipolar depression. It is often used off-label for treating anxiety conditions and as an augmentation agent for treatment-resistant depression. However, its benefit in depression with comorbid anxiety disorders has not been systematically evaluated. The current study evaluated the benefit and tolerability of quetiapine as augmentation to first-line antidepressants for MDD comorbid with anxiety disorders.

Methods: In this multicenter trial (June 2008-June 2013), 76 adults (aged 18-65 years) with a primary diagnosis of unipolar depression comorbid with at least 1 anxiety disorder (per DSM-IV-TR criteria) received flexible-dose quetiapine extended-release (XR) 50-300 mg/d or placebo as add-on for 12 weeks in a 2:1 ratio. Depression, anxiety, life satisfaction, and adverse events were assessed.

Results: Depression, anxiety, and function improved significantly in both groups. On primary outcome measures, quetiapine was superior to placebo in improving depression (17-item Hamilton Depression Rating Scale score: mean difference = -3.64; 95% CI, -7.01 to -0.27) and anxiety symptoms (Hamilton Anxiety Rating Scale score: mean difference = -4.02; 95% CI, -7.41 to -0.64), as well as Clinical Global Impressions-Severity of Illness scale score (mean difference = -0.64; 95% CI, -1.13 to -0.15). On secondary measures including the Montgomery-Asberg Depression Rating Scale, Beck Depression Inventory, Penn State Worry Questionnaire, and Quality of Life Satisfaction and Enjoyment Questionnaire, quetiapine produced a greater degree of improvement compared to placebo, but group differences were not statistically significant. Quetiapine was well tolerated, with mostly minor and no serious adverse effects.

Conclusions: Quetiapine augmentation may be a useful intervention for MDD with comorbid anxiety.

Trial Registration: ClinicalTrials.gov Identifier: NCT00688818.

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