Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.
Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.
J Affect Disord. 2022 Jan 1;296:485-492. doi: 10.1016/j.jad.2021.09.063. Epub 2021 Sep 25.
We aimed to investigate the prescription pattern of pregabalin augmentation of antidepressants in major depressive disorder (MDD) and to explore variables associated with add-on pregabalin treatment.
1410 MDD patients participated in this naturalistic European multicenter study with retrospective assessment of treatment response. Analyses of covariance, chi-squared tests, and binary logistic regressions were accomplished to determine differences in socio-demographic and clinical characteristics between MDD patients with and without pregabalin augmentation.
Add-on pregabalin was established in 102 (7.23%) MDD patients. Compared to those without receiving pregabalin, pregabalin-treated patients were characterized by a significantly higher likelihood for older age (mean: 54.74 ± 13.08 vs 49.93 ± 14.13 years), unemployment (78.43% vs 51.23%), melancholic features (83.33% vs 58.94%), inpatient treatment (72.55% vs 31.65%), previous psychiatric hospitalizations (13.52 ± 24.82 vs 4.96 ± 19.93 weeks), any somatic comorbidity (68.63% vs 44.57%), comorbid hypertension (37.25% vs 17.51%), more severe depressive symptom severity at the onset of the current episode (mean MADRS: 37.55 ± 9.00 vs 33.79 ± 7.52), receiving augmentation/combination treatment strategies in general (mean number of psychotropic drugs: 3.64 ± 0.92 vs 2.07 ± 1.17), and with antidepressants (50.00% vs 27.91%) and antipsychotics (46.08% vs 24.08%) in particular.
Due to its observational cross-sectional study design, our patient sample might not be fully representative for MDD patients in primary care settings.
Our findings suggest that add-on pregabalin is particularly administered in more severe/difficult-to-treat MDD conditions, whereas no association between the prescription of adjunctive pregabalin and comorbid anxiety symptoms could be determined.
我们旨在研究普瑞巴林在治疗重度抑郁症(MDD)中的加用情况,并探讨与加用普瑞巴林治疗相关的变量。
1410 例 MDD 患者参与了这项回顾性评估治疗反应的欧洲多中心自然主义研究。采用协方差分析、卡方检验和二项逻辑回归来确定 MDD 患者中有无普瑞巴林加用的社会人口学和临床特征差异。
102 例(7.23%)MDD 患者加用了普瑞巴林。与未接受普瑞巴林治疗的患者相比,接受普瑞巴林治疗的患者年龄明显较大(平均:54.74±13.08 岁 vs 49.93±14.13 岁)、失业(78.43% vs 51.23%)、忧郁特征(83.33% vs 58.94%)、住院治疗(72.55% vs 31.65%)、以前的精神病院住院治疗(13.52±24.82 周 vs 4.96±19.93 周)、任何躯体合并症(68.63% vs 44.57%)、合并高血压(37.25% vs 17.51%)、当前发作起始时抑郁症状严重程度更严重(平均 MADRS:37.55±9.00 分 vs 33.79±7.52 分)、总体上接受增效/联合治疗策略(平均精神药物数量:3.64±0.92 种 vs 2.07±1.17 种)以及抗抑郁药(50.00% vs 27.91%)和抗精神病药(46.08% vs 24.08%)的比例较高。
由于其观察性横断面研究设计,我们的患者样本可能无法完全代表初级保健环境中的 MDD 患者。
我们的研究结果表明,普瑞巴林加用主要用于更严重/治疗困难的 MDD 情况,而无法确定普瑞巴林辅助治疗与合并焦虑症状之间的相关性。