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Efficacy, acceptability, and safety of adjunctive aripiprazole in treatment-resistant depression: a meta-analysis of randomized controlled trials. | LitMetric

Efficacy, acceptability, and safety of adjunctive aripiprazole in treatment-resistant depression: a meta-analysis of randomized controlled trials.

Neuropsychiatr Dis Treat

Department of Physiology, College of Basic Medical Sciences, Jilin University, Changchun, China.

Published: February 2018

AI Article Synopsis

  • Treatment-resistant depression (TRD) is serious and common in adults, leading researchers to analyze the effectiveness and safety of adding aripiprazole to existing treatments through a meta-analysis of various randomized controlled trials (RCTs).
  • The study included data from 8 RCTs with 2,260 patients, finding that aripiprazole significantly increased both remission and response rates compared to other treatments, along with more notable improvements in depression rating scales.
  • However, patients receiving aripiprazole experienced a higher rate of discontinuation due to adverse events, indicating that while it may be effective, it also comes with greater risks of side effects.

Article Abstract

Background: Treatment-resistant depression (TRD) is common and potentially life-threatening in adults, and the benefits and risks of adjunctive aripiprazole in these patients remain controversial. Therefore, we conducted a meta-analysis of randomized controlled trials (RCTs) to assess the efficacy, acceptability, safety, and quality of life of adjunctive aripiprazole in patients with TRD.

Methods: RCTs published in PubMed, Web of Science, and Embase were systematically reviewed to evaluate the efficacy and safety profiles of TRD patients who were treated with adjunctive aripiprazole. The main outcome measures included response rate, remission rate, changes from baseline in Montgomery-Asberg Depression Rating Scale (MADRS), Clinical Global Impression-severity (CGI-S), Clinical Global Impression-improvement (CGI-I), 17-Item Hamilton Rating Scale for Depression (HAM-D17), Sheehan Disability scale (SDS), and Inventory of Depressive Symptomatology Self-Report Scale (IDS-SR), discontinuation due to adverse events, and adverse events. Risk ratio (RR) or weight mean difference with 95% confidence intervals (CIs) were pooled using a fixed-effects or random-effects model according to the heterogeneity among studies.

Results: A total of 8 RCTs involving 2,260 patients were included in this meta-analysis. Adjunctive aripiprazole was associated with a significantly higher remission rate (RR =1.64, 95% CI: 1.42 to 1.89; <0.001) and response rate (RR =1.45, 95% CI: 1.13 to 1.87; =0.004) than other treatments. Moreover, adjunctive aripiprazole had greater changes in MADRS score, CGI-S score, CGI-I score, HAM-D17 score, SDS score, and IDS-SR score. There were more patients treated with adjunctive aripiprazole who discontinued their treatments due to adverse events. The incidence of adverse events was significantly higher in the adjunctive aripiprazole group than in other treatment groups.

Conclusion: The adjunctive aripiprazole showed benefits in improving the response rate, remission rate, and the quality of life in patients with TRD. However, clinicians should interpret these findings with caution due to the evidence of potential treatment-related side effects.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5810518PMC
http://dx.doi.org/10.2147/NDT.S156619DOI Listing

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