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A double-blind randomized placebo-controlled study of low dose mirtazapine once daily in patients of major depressive disorders on escitalopram

机译:依西酞普兰主要抑郁症患者每天一次低剂量米氮平的双盲随机安慰剂对照研究

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Background: The SSRIs being used as 1 st line therapy in treatment of depression have delayed therapeutic effect which makes the patient vulnerable to an increased risk of suicide and decreased adherence to the treatment and will prematurely discontinue the therapy. The present study was conducted to evaluate if low dose mirtazapine-escitalopram combination therapy has any add on benefit over monotherapy with escitalopram. Methods: In a single-centered, comparative study involving patients with depression attending the out-patient after screening and exclusion, 60 eligible patients were randomly assigned to receive tablet mirtazapine 7.5 mg plus tablet escitalopram 10 mg intervention or tablet escitalopram 10 mg plus placebo intervention in a double-blind 6-week treatment phase. The primary outcome measure was the change in the 17-item Hamilton Depression Rating Scale (HDRS) and Montgomery-Asberg Depression Rating Scale (MADRS) score from baseline. Participants were evaluated at baseline, 1 st , 2 nd ,4 th and 6 th week. Results were analyzed using Chi-Square test for adverse effects and independent t-test analysis for efficacy parameter. Results: In the analysis of results at 6 th week the numbers of patients achieved remission in mirtazapine group are more with a p-value of 0.018 which is significant and the numbers of responders in mirtazapine group are also more which is statistically significant on chi-square test. There is no significant difference was observed between the two groups with reference to occurrence of adverse effect. Conclusions: Adding low dose mirtazapine has an added benefit in terms of efficacy and getting remission early with more number of responders in the treatment of major depression.
机译:背景:SSRIs被用作抑郁症的一线治疗药物,具有延迟的治疗作用,这使患者容易遭受自杀风险的增加和对治疗的依从性下降,并将过早中断治疗。本研究旨在评估低剂量米氮平-艾司西酞普兰联合治疗是否比艾司西酞普兰单药治疗有更多益处。方法:在一项涉及抑郁症患者的单中心比较研究中,筛选和排除抑郁症的患者在门诊就诊,将60名符合条件的患者随机分配接受米氮平7.5毫克加艾司西酞普兰10毫克片剂或艾司西酞普兰10毫克加安慰剂干预在为期6周的双盲治疗阶段。主要结局指标是汉密尔顿抑郁量表(HDRS)和蒙哥马利-阿斯伯格抑郁量表(MADRS)得分与基线相比的变化(共17个项目)。在基线,第1、2、4和6周对参与者进行评估。使用卡方检验对不良反应进行分析,对功效参数进行独立的t检验分析。结果:在第6周的结果分析中,米氮平组的患者缓解率更高,p值为0.018,这是显着的;米氮平组的反应者数量也更多,对卡地尔来说,统计学上具有统计学意义。方格测试。关于不良反应的发生,两组之间没有观察到显着差异。结论:在重症抑郁症治疗中,添加低剂量米氮平具有更大的益处,并且可以使早期缓解,并且有更多的反应者。

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