TY - JOUR
T1 - Antipsychotic Monotherapy for Major Depressive Disorder
T2 - A Systematic Review and Meta-Analysis
AU - Nishi, Akira
AU - Sawada, Kyosuke
AU - Uchida, Hiroyuki
AU - Mimura, Masaru
AU - Takeuchi, Hiroyoshi
N1 - Publisher Copyright:
© 2022. Thieme. All rights reserved.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Although several randomized controlled trials (RCTs) have compared the effectiveness, efficacy, and safety of antipsychotic monotherapy (APM) versus placebo in patients with major depressive disorder (MDD), no meta-analysis has examined this topic. We conducted a systematic literature search using MEDLINE and Embase to identify relevant RCTs and performed a meta-analysis to compare the following outcomes between APM and placebo: response and remission rates, study discontinuation due to all causes, lack of efficacy, and adverse events, changes in total scores on depression severity scales, and individual adverse event rates. A total of 13 studies were identified, with 14 comparisons involving 3,197 participants that met the eligibility criteria. There were significant differences between APM and placebo in response and remission rates and changes in the primary depression severity scale in favor of APM, and study discontinuation due to adverse events and several individual adverse events in favor of placebo. No significant difference was observed in discontinuation due to all causes. APM could have antidepressant effects in the acute phase of MDD, although clinicians should be aware of an increased risk of some adverse events.
AB - Although several randomized controlled trials (RCTs) have compared the effectiveness, efficacy, and safety of antipsychotic monotherapy (APM) versus placebo in patients with major depressive disorder (MDD), no meta-analysis has examined this topic. We conducted a systematic literature search using MEDLINE and Embase to identify relevant RCTs and performed a meta-analysis to compare the following outcomes between APM and placebo: response and remission rates, study discontinuation due to all causes, lack of efficacy, and adverse events, changes in total scores on depression severity scales, and individual adverse event rates. A total of 13 studies were identified, with 14 comparisons involving 3,197 participants that met the eligibility criteria. There were significant differences between APM and placebo in response and remission rates and changes in the primary depression severity scale in favor of APM, and study discontinuation due to adverse events and several individual adverse events in favor of placebo. No significant difference was observed in discontinuation due to all causes. APM could have antidepressant effects in the acute phase of MDD, although clinicians should be aware of an increased risk of some adverse events.
KW - antipsychotics
KW - major depressive disorder
KW - meta-analysis
KW - monotherapy
KW - systematic review
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U2 - 10.1055/a-1934-9856
DO - 10.1055/a-1934-9856
M3 - Review article
C2 - 36257518
AN - SCOPUS:85141871701
SN - 0176-3679
VL - 56
SP - 5
EP - 17
JO - Pharmakopsychiatrie und Neuropsychopharmakologie
JF - Pharmakopsychiatrie und Neuropsychopharmakologie
IS - 1
ER -