Department of Mental Health, Psychiatric Service of Diagnosis and Treatment, Hospital "G. Mazzini," National Health Service (NHS), ASL 4 Teramo, Italy.
Department of Neurosciences and Imaging, University "G. D'Annunzio" Chieti, Italy.
Braz J Psychiatry. 2020;42(3):317-321. doi: 10.1590/1516-4446-2019-0690. Epub 2020 Mar 9.
Selective serotonin reuptake inhibitors (SSRIs) are the cornerstone of treatment of major depressive disorder (MDD). However, non-response is common, often necessitating combination strategies. The present study assessed the efficacy of vortioxetine as an add-on therapy in patients with SSRI-resistant MDD.
The charts of 36 adult outpatients with DSM-IV-TR MDD who had not achieved a response after at least 8 weeks of treatment with an SSRI were reviewed retrospectively. Subjects were treated with vortioxetine (5-20 mg/day) for 8 weeks added to the current SSRI. The main outcome measures were change from baseline in total Hamilton Scale for Depression (HAM-D) score and the rate of response (a 50% or greater reduction in HAM-D score and a Clinical Global Impression - Improvement module [CGI-I] score of 1 or 2 at endpoint). HAM-D scores ≤ 7 were considered as remission. Additional outcome measures included the Snaith-Hamilton Pleasure Scale (SHAPS) and the Scale for Suicide Ideation (SSI).
32 patients completed the 8 weeks of treatment. At 8 weeks, a significant reduction in HAM-D score was observed (p ≤ 0.001), with response obtained by 41.7% and remission by 33.3% of patients. Significant reductions in SHAPS and SSI were also observed (p ≤ 0.001 for both scales).
Adjunctive vortioxetine may be useful and well-tolerated in stage I treatment-resistant depression. However, the limitations of this study (such as small sample size, absence of randomization and control group, retrospective design, etc.) must be considered.
选择性 5-羟色胺再摄取抑制剂(SSRIs)是治疗重度抑郁症(MDD)的基石。然而,无反应很常见,通常需要联合治疗策略。本研究评估了文拉法辛作为 SSRI 抵抗性 MDD 患者附加治疗的疗效。
回顾性分析了 36 名成年门诊 DSM-IV-TR MDD 患者的图表,这些患者在至少 8 周的 SSRI 治疗后未达到反应。患者接受文拉法辛(5-20mg/天)治疗 8 周,同时加用当前的 SSRI。主要结局指标是从基线到总汉密尔顿抑郁量表(HAM-D)评分的变化和反应率(HAM-D 评分降低 50%或更多,临床总体印象-改善模块[CGI-I]评分在终点时为 1 或 2)。HAM-D 评分≤7 被认为是缓解。其他结局指标包括 Snaith-Hamilton 愉悦量表(SHAPS)和自杀意念量表(SSI)。
32 名患者完成了 8 周的治疗。在 8 周时,HAM-D 评分显著降低(p≤0.001),41.7%的患者获得反应,33.3%的患者缓解。SHAPS 和 SSI 也显著降低(两个量表均为 p≤0.001)。
辅助文拉法辛可能对 I 期治疗抵抗性抑郁症有用且耐受良好。然而,必须考虑到本研究的局限性(如样本量小、无随机分组和对照组、回顾性设计等)。