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Systematic review and meta-analysis of augmentation and combination treatments for early-stage treatment-resistant depression.

Authors :
Scott F
Hampsey E
Gnanapragasam S
Carter B
Marwood L
Taylor RW
Emre C
Korotkova L
Martín-Dombrowski J
Cleare AJ
Young AH
Strawbridge R
Source :
Journal of psychopharmacology (Oxford, England) [J Psychopharmacol] 2023 Mar; Vol. 37 (3), pp. 268-278. Date of Electronic Publication: 2022 Jul 21.
Publication Year :
2023

Abstract

Background: Major depressive disorder (MDD) is a highly burdensome health condition, for which there are numerous accepted pharmacological and psychological interventions. Adjunctive treatment (augmentation/combination) is recommended for the ~50% of MDD patients who do not adequately respond to first-line treatment. We aimed to evaluate the current evidence for concomitant approaches for people with early-stage treatment-resistant depression (TRD; defined below).<br />Methods: We systematically searched Medline and Institute for Scientific Information Web of Science to identify randomised controlled trials of adjunctive treatment of ⩾10 adults with MDD who had not responded to ⩾1 adequate antidepressant. The cochrane risk of bias (RoB) tool was used to assess study quality. Pre-post treatment meta-analyses were performed, allowing for comparison across heterogeneous study designs independent of comparator interventions.<br />Results: In total, 115 trials investigating 48 treatments were synthesised. The mean intervention duration was 9 weeks (range 5 days to 18 months) with most studies assessed to have low ( n  = 57) or moderate ( n  = 51) RoB. The highest effect sizes (ESs) were from cognitive behavioural therapy (ES = 1.58, 95% confidence interval (CI): 1.09-2.07), (es)ketamine (ES = 1.48, 95% CI: 1.23-1.73) and risperidone (ES = 1.42, 95% CI: 1.29-1.61). Only aripiprazole and lithium were examined in ⩾10 studies. Pill placebo (ES = 0.89, 95% CI: 0.81-0.98) had a not inconsiderable ES, and only six treatments' 95% CIs did not overlap with pill placebo's (aripiprazole, (es)ketamine, mirtazapine, olanzapine, quetiapine and risperidone). We report marked heterogeneity between studies for almost all analyses.<br />Conclusions: Our findings support cautious optimism for several augmentation strategies; although considering the high prevalence of TRD, evidence remains inadequate for each treatment option.

Details

Language :
English
ISSN :
1461-7285
Volume :
37
Issue :
3
Database :
MEDLINE
Journal :
Journal of psychopharmacology (Oxford, England)
Publication Type :
Academic Journal
Accession number :
35861202
Full Text :
https://doi.org/10.1177/02698811221104058