Effectiveness of mirtazapine as add-on to paroxetine v. paroxetine or mirtazapine monotherapy in patients with major depressive disorder with early non-response to paroxetine: a two-phase, multicentre, randomized, double-blind clinical trial

米氮平 帕罗西汀 哈姆德 安慰剂 重性抑郁障碍 内科学 心理学 随机对照试验 不利影响 医学 精神科 抗抑郁药 显著性差异 焦虑 心情 替代医学 病理
作者
Le Xiao,Xuequan Zhu,Amy Gillespie,Yuan Feng,Jingjing Zhou,Xu Chen,Yuanyuan Gao,Xueyi Wang,Xiancang Ma,Chengge Gao,Yunshi Xie,Xiaoping Pan,Yan Bai,Xiufeng Xu,Gang Wang,Runsen Chen
出处
期刊:Psychological Medicine [Cambridge University Press]
卷期号:51 (7): 1166-1174 被引量:14
标识
DOI:10.1017/s0033291719004069
摘要

Abstract Background This study aimed to examine the efficacy of combining paroxetine and mirtazapine v. switching to mirtazapine, for patients with major depressive disorder (MDD) who have had an insufficient response to SSRI monotherapy (paroxetine) after the first 2 weeks of treatment. Methods This double-blind, randomized, placebo-controlled, three-arm study recruited participants from five hospitals in China. Eligible participants were aged 18–60 years with MDD of at least moderate severity. Participants received paroxetine during a 2-week open-label phase and patients who had not achieved early improvement were randomized to paroxetine, mirtazapine or paroxetine combined with mirtazapine for 6 weeks. The primary outcome was improvement on the Hamilton Rating Scale for Depression 17-item (HAMD-17) scores 6 weeks after randomization. Results A total of 204 patients who showed early non-response to paroxetine monotherapy were randomly assigned to receive either mirtazapine and placebo ( n = 68), paroxetine and placebo ( n = 68) or mirtazapine and paroxetine ( n = 68), with 164 patients completing the outcome assessment. At week 8, the least squares (LS) mean change of HAMD-17 scores did not significantly differ among the three groups, (12.98 points) in the mirtazapine group, (12.50 points) in the paroxetine group and (13.27 points) in the mirtazapine plus paroxetine combination group. Participants in the paroxetine monotherapy group were least likely to experience adverse effects. Conclusions After 8 weeks follow-up, paroxetine monotherapy, mirtazapine monotherapy and paroxetine/mirtazapine combination therapy were equally effective in non-improvers at 2 weeks. The results of this trial do not support a recommendation to routinely offer additional treatment or a switch in treatment strategies for MDD patients who do not show early improvement after 2 weeks of antidepressant treatment.
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