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  3. Comparative Efficacy and Acceptability of Treatment Strategies for Antipsychotic-Induced Akathisia: A Systematic Review and Network Meta-analysis.
 

Comparative Efficacy and Acceptability of Treatment Strategies for Antipsychotic-Induced Akathisia: A Systematic Review and Network Meta-analysis.

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BORIS DOI
10.48350/197829
Publisher DOI
10.1093/schbul/sbae098
PubMed ID
38869177
Description
BACKGROUND

Antipsychotics are the treatment of choice for schizophrenia, but they often induce akathisia. However, comparative efficacy of treatment strategies for akathisia remains unclear.

DESIGN

We performed a systematic review and network meta-analyses (PROSPERO CRD42023450720). We searched multiple databases on July 24, 2023. We included randomized clinical trials comparing 1 or more treatment strategies for antipsychotic-induced akathisia against each other or control conditions. We included adults with schizophrenia or other psychiatric disorders treated with antipsychotics. The primary outcome was akathisia severity at posttreatment. Secondary outcomes included akathisia response, all-cause dropout, psychotic symptoms, and long-term akathisia severity. We synthesized data in random effects frequentist network meta-analyses and assessed confidence in the evidence using CINeMA.

RESULTS

We identified 19 trials with 661 randomized participants (mean age 35.9 [standard deviation 12.0]; 36.7% [195 of 532] women). No trials examined dose reduction or switching of antipsychotics. Findings suggested 5-HT2A antagonists (k = 6, n = 108; standardized mean difference [SMD] -1.07 [95% confidence interval, -1.42; -0.71]) and beta-blockers (k = 8, n = 105; SMD -0.46 [-0.85; -0.07]) may improve akathisia severity, but confidence in the evidence was deemed low. We also found that benzodiazepines (k = 2, n = 13; SMD -1.62 [-2.64; -0.59]) and vitamin B6 (k = 3, n = 67; SMD -0.99 [-1.49; -0.50]) might also be beneficial, but confidence in the evidence was very low. Analyses of secondary outcomes did not provide additional insights.

CONCLUSIONS

Our findings suggest that 5-HT2A antagonists, beta-blockers, and with a lesser certainty, benzodiazepines, and vitamin B6 might improve akathisia. Given the low to very low confidence in the evidence of add-on agents and the absence of evidence of their long-term efficacy, careful consideration of side effects is warranted. These recommendations are extremely preliminary and further trials are needed.
Date of Publication
2026-03-07
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
300 Social sciences, sociology & anthropology > 360 Social problems & social services
Keyword(s)
Akathisia antipsychotic network meta-analysis schizophrenia
Language(s)
en
Contributor(s)
Furukawa, Yuki
Imai, Kota
Takahashi, Yusuke
Efthimiou, Orestisorcid-logo
Berner Institut für Hausarztmedizin (BIHAM)
Institut für Sozial- und Präventivmedizin (ISPM) - HIV, Hepatitis & Tubercolosis
Institut für Sozial- und Präventivmedizin (ISPM) - IeDEA
Leucht, Stefan
Additional Credits
Institut für Sozial- und Präventivmedizin (ISPM) - HIV, Hepatitis & Tubercolosis
Berner Institut für Hausarztmedizin (BIHAM)
Institut für Sozial- und Präventivmedizin (ISPM) - IeDEA
Series
Schizophrenia Bulletin: The Journal of Psychoses and Related Disorders
Publisher
Oxford University Press
ISSN
0586-7614
Access(Rights)
open.access
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