Department of Biostatistics and Health Informatics, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London.
Department of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Int Rev Psychiatry. 2020 Aug-Sep;32(5-6):477-490. doi: 10.1080/09540261.2020.1765748. Epub 2020 Jun 5.
Most interventions for treatment-resistant depression (TRD) are added as augmenters. We aimed to determine the relative effectiveness of augmentation treatments for TRD. This systematic review and network meta-analysis (NMA) sought all randomized trials of pharmacological and psychological augmentation interventions for adults meeting the most common clinical criteria for TRD. The NMA compared the intervention effectiveness of depressive symptoms for TRD augmentation. Of 36 included trials, 27 were suitable for inclusion in NMA, and no psychological trials could be included in the absence of a common comparator. Antipsychotics (13 trials), mood stabilizers (three trials), NMDA-targeting medications (five trials), and other mechanisms (3 trials) were compared against placebo. NMDA treatments were markedly superior to placebo (ES = 0.91, 95% CI 0.67 to 1.16) and head-to-head NMA suggested that NMDA therapies had the highest chance of being an effective treatment option compared to other pharmacological classes. This study provides the most comprehensive evidence of augmenters' effectiveness for TRD, and our GRADE recommendations can be used to guide guidelines to optimize treatment choices. Although conclusions are limited by paucity of, and heterogeneity between, trials as well as inconsistent reports of treatment safety. This work supports the use of NMDA-targeting medications such as ketamine.
大多数治疗抵抗性抑郁症(TRD)的干预措施都作为增效剂添加。我们旨在确定 TRD 增效治疗的相对有效性。这项系统评价和网络荟萃分析(NMA)搜索了所有符合 TRD 最常见临床标准的成年人接受药理学和心理增效干预的随机试验。NMA 比较了 TRD 增效的抑郁症状干预效果。在 36 项纳入的试验中,27 项适合纳入 NMA,由于缺乏共同的对照,无法纳入心理试验。抗精神病药(13 项试验)、心境稳定剂(3 项试验)、NMDA 靶向药物(5 项试验)和其他机制(3 项试验)与安慰剂进行了比较。NMDA 治疗明显优于安慰剂(ES=0.91,95%CI 0.67 至 1.16),头对头 NMA 表明,与其他药物类别相比,NMDA 疗法最有可能成为有效的治疗选择。本研究提供了 TRD 增效剂有效性的最全面证据,我们的 GRADE 建议可用于指导指南,以优化治疗选择。尽管结论受到试验数量少、异质性以及治疗安全性报告不一致的限制。这项工作支持使用 NMDA 靶向药物,如氯胺酮。