Clinical Research Center, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, China; School of Public Health, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Unit of Psychiatry, Faculty of Health Sciences, University of Macau, Macao, SAR, China.
J Psychiatr Res. 2019 Nov;118:21-30. doi: 10.1016/j.jpsychires.2019.08.009. Epub 2019 Aug 16.
The guide recommends SSRI and SNRI drugs as first-line treatments for generalized anxiety disorder (GAD). Therefore, we aimed to update the evidence using network meta-analysis by comparing the efficacy and acceptability of first-line drugs. The relevant electronic databases were searched for placebo-controlled and head-to-head trials of 11 drugs used for the acute treatment of adults with GAD from 1980 up to January 1, 2019. Data on demographics, clinical, and treatment information were extracted from each eligible study. The primary outcomes were efficacy (quantified as the change in the total score on the Hamilton Anxiety Scale from baseline) and acceptability (quantified as treatment discontinuations due to any cause). Overall, the data on 41 RCTs were sufficient or appropriate for inclusion. In terms of efficacy, all of the drugs except fluoxetine and vortioxetine were more effective than placebo, with the weighted mean difference of the Hamilton Anxiety Scale score ranging between -3.2 (95% credible interval [CrI] = -4.2 to -2.2) for escitalopram and -1·8 (95% CrI = -3.1 to -0.55) for vilazodone. For acceptability, only vilazodone (OR = 1.7, 95% CrI = 1.1 to 2.7) were worse than placebo, others did not show significant differences from placebo. In head-to-head comparisons, vortioxetine showed better acceptability and tolerability but worse efficacy and response rate. In conclusion, most drugs are more effective than placebo, and there are few significant differences between the active drugs and placebo on acceptability. Overall, duloxetine and escitalopram showed better efficacy while vortioxetine showed better acceptability.
该指南建议将 SSRI 和 SNRIs 类药物作为广泛性焦虑障碍(GAD)的一线治疗药物。因此,我们旨在通过比较一线药物的疗效和可接受性,使用网络荟萃分析更新证据。从 1980 年至 2019 年 1 月 1 日,我们对 11 种用于治疗成人 GAD 急性发作的药物的安慰剂对照和头对头试验进行了相关电子数据库检索。从每个合格的研究中提取人口统计学、临床和治疗信息的数据。主要结局是疗效(通过汉密尔顿焦虑量表总分从基线的变化来量化)和可接受性(通过任何原因导致的治疗中断来量化)。总体而言,有足够或适当的数据可纳入 41 项 RCT。在疗效方面,除氟西汀和文拉法辛外,所有药物均优于安慰剂,汉密尔顿焦虑量表评分的加权均数差介于依他普仑(-3.2,95%可信区间 [CrI]:-4.2 至-2.2)和维拉唑酮(-1.8,95% CrI:-3.1 至-0.55)之间。对于可接受性,只有维拉唑酮(OR=1.7,95% CrI:1.1 至 2.7)比安慰剂差,其他药物与安慰剂之间无显著差异。在头对头比较中,文拉法辛显示出更好的可接受性和耐受性,但疗效和应答率更差。总之,大多数药物比安慰剂更有效,而活性药物与安慰剂在可接受性方面的差异较小。总体而言,度洛西汀和依他普仑显示出更好的疗效,而文拉法辛显示出更好的可接受性。