Interventional Psychiatry Program, St. Michael's Hospital, Toronto, Ontario, Canada.
Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.
Brain Behav. 2022 May;12(5):e2555. doi: 10.1002/brb3.2555. Epub 2022 Mar 25.
To report side effect frequency and severity in patients with major depressive disorder (MDD) receiving escitalopram and aripiprazole adjunctive therapy and to examine whether pretreatment anxious depression is associated with the number and presence of specific side effects.
188 of the 211 trial participants provided information on side effects during treatment with escitalopram (10-20 mg) for 8 weeks, and nonresponders received further augmentation on aripiprazole (2-10 mg) adjunctive therapy for another 8 weeks, whereas responders remained on escitalopram. Participants completed the Toronto Side Effects Scale at weeks 2, 4, 10, and 12. Covariate-adjusted negative binomial regression and Wilcoxon tests examined the association between anxious depression (GAD-7 ≥ 10) and number of side effects. Covariate-adjusted logistic regression and chi-square tests explored the association between anxious depression and specific side effects.
For both therapies, the most frequent side effects were also the most severe. They mostly related to the central nervous system (CNS) (i.e., drowsiness and nervousness). Between baseline and week 2, the number of side effects participants experienced (incidence rate ratio [IRR] = 1.38, p = .010) or had trouble with (IRR = 1.34, p = .026) was significantly higher among those with anxious depression for escitalopram but not adjunctive aripiprazole. Further, odds of experiencing and having trouble with nervousness and agitation were also significantly higher in anxious depression for escitalopram only (p < .05).
Patients on escitalopram and aripiprazole adjunctive therapy may experience and have trouble with CNS side effects. Pretreatment anxious depression may predispose escitalopram recipients with MDD to developing side effects, especially those related to anxiety.
报告接受艾司西酞普兰和阿立哌唑辅助治疗的重度抑郁症(MDD)患者的不良反应频率和严重程度,并探讨治疗前焦虑抑郁是否与特定不良反应的数量和出现有关。
188 名试验参与者中的 211 名在接受艾司西酞普兰(10-20mg)治疗 8 周期间提供了不良反应信息,无应答者在阿立哌唑(2-10mg)辅助治疗的基础上再接受 8 周治疗,而应答者继续接受艾司西酞普兰治疗。参与者在第 2、4、10 和 12 周完成多伦多不良反应量表。协变量调整的负二项回归和 Wilcoxon 检验检查了焦虑抑郁(GAD-7≥10)与不良反应数量之间的关联。协变量调整的逻辑回归和卡方检验探讨了焦虑抑郁与特定不良反应之间的关系。
对于两种治疗方法,最常见的不良反应也是最严重的。它们主要与中枢神经系统(CNS)有关(即,嗜睡和紧张)。与基线相比,在第 2 周,经历不良反应的参与者数量(发生率比[IRR] = 1.38,p = 0.010)或出现不良反应的参与者数量(IRR = 1.34,p = 0.026)在有焦虑抑郁的患者中显著更高艾司西酞普兰,但不是阿立哌唑辅助治疗。此外,在有焦虑抑郁的患者中,出现紧张和激动的几率也显著更高,仅在艾司西酞普兰中(p<0.05)。
接受艾司西酞普兰和阿立哌唑辅助治疗的患者可能会经历中枢神经系统不良反应,并出现不良反应。治疗前的焦虑抑郁可能使 MDD 患者更容易出现艾司西酞普兰的不良反应,尤其是与焦虑相关的不良反应。