Akathisia and Newer Second-Generation Antipsychotic Drugs: A Review of Current Evidence
- PMID: 32342999
- DOI: 10.1002/phar.2404
Akathisia and Newer Second-Generation Antipsychotic Drugs: A Review of Current Evidence
Abstract
Akathisia continues to present a significant challenge in clinical practice. As a class, so-called atypical, or second-generation, antipsychotics (SGAs) are the mainstay of treatment for schizophrenia and are commonly used to treat mood disorders. These medications have traditionally been distinguished from first-generation antipsychotics by their lowered risk of extrapyramidal side effects (EPS) such as dystonia, dyskinesia, akathisia, and pseudoparkinsonism. However, the occurrence of EPS, particularly akathisia, has been demonstrated to some degree in all commercially available SGAs. This review examines the incidence of akathisia in nine newer SGAs in patients with schizophrenia, bipolar disorder, and major depressive disorder (MDD). We performed a search of PubMed, ClinicalTrials.gov, Cochrane Central Register, and Google Scholar, as well as manufacturer websites and product labeling for published and unpublished clinical trials, meta-analyses, and systematic reviews. Studies evaluating adult patients with schizophrenia, bipolar disorder, or MDD were eligible for inclusion. Data on treatment-emergent akathisia rates were gathered from each study, and potential dose-response relationships were explored. A total of 177 studies were included in this review, comprising 58,069 patients across 414 treatment arms. Compared with placebo with a composite 3.7% incidence of akathisia, individual SGAs produced akathisia at total composite rates ranging from 2.9-13.0% across the included studies. High doses of an SGA were generally associated with an increased risk of akathisia. Clinicians should consider the risk of akathisia when choosing a treatment option and monitor for akathisia in patients beginning therapy with an SGA or following a dose increase of the SGA.
Keywords: akathisia; antipsychotics; bipolar disorder; major depressive disorder; schizophrenia.
© 2020 Pharmacotherapy Publications, Inc.
Similar articles
-
Medication-Induced Akathisia with Newly Approved Antipsychotics in Patients with a Severe Mental Illness: A Systematic Review and Meta-Analysis.CNS Drugs. 2019 Jun;33(6):549-566. doi: 10.1007/s40263-019-00625-3. CNS Drugs. 2019. PMID: 31065941
-
Akathisia: an updated review focusing on second-generation antipsychotics.J Clin Psychiatry. 2009 Apr 21;70(5):627-43. doi: 10.4088/JCP.08r04210. J Clin Psychiatry. 2009. PMID: 19389331 Review.
-
EPS profiles: the atypical antipsychotics are not all the same.J Psychiatr Pract. 2007 Jan;13(1):13-24. doi: 10.1097/00131746-200701000-00003. J Psychiatr Pract. 2007. PMID: 17242588 Review.
-
Number needed to treat to harm for discontinuation due to adverse events in the treatment of bipolar depression, major depressive disorder, and generalized anxiety disorder with atypical antipsychotics.J Clin Psychiatry. 2011 Aug;72(8):1063-71. doi: 10.4088/JCP.09r05535gre. Epub 2010 Oct 19. J Clin Psychiatry. 2011. PMID: 21034695 Free PMC article.
-
The Incidence of Akathisia in the Treatment of Schizophrenia with Aripiprazole, Asenapine and Lurasidone: A Meta-Analysis.Curr Neuropharmacol. 2015;13(5):681-91. doi: 10.2174/1570159x13666150115220221. Curr Neuropharmacol. 2015. PMID: 26467415 Free PMC article. Review.
Cited by
-
Effect of single-administration of D-sorbitol pretreatment on the bitterness and continued willingness to take asenapine: a randomized, single-blind, placebo-controlled, crossover trial.BMC Psychiatry. 2024 Jan 30;24(1):81. doi: 10.1186/s12888-024-05549-x. BMC Psychiatry. 2024. PMID: 38291403 Free PMC article. Clinical Trial.
-
Single-Nucleotide Polymorphisms as Biomarkers of Antipsychotic-Induced Akathisia: Systematic Review.Genes (Basel). 2023 Feb 28;14(3):616. doi: 10.3390/genes14030616. Genes (Basel). 2023. PMID: 36980888 Free PMC article. Review.
-
Sensory evaluation of the bitterness of asenapine using D-sorbitol pretreatment: single-blind, placebo-controlled, crossover trial.BMC Psychiatry. 2023 Mar 14;23(1):159. doi: 10.1186/s12888-023-04664-5. BMC Psychiatry. 2023. PMID: 36918838 Free PMC article. Clinical Trial.
-
Effectiveness and safety of blonanserin in young and middle-aged female patients with schizophrenia: data from a post-marketing surveillance.BMC Psychiatry. 2023 Feb 21;23(1):115. doi: 10.1186/s12888-023-04598-y. BMC Psychiatry. 2023. PMID: 36810039 Free PMC article.
-
Amisulpride withdrawal akathisia responding to aripiprazole with propranolol in first-onset psychosis: a case report.BMC Psychiatry. 2022 Jan 29;22(1):74. doi: 10.1186/s12888-022-03721-9. BMC Psychiatry. 2022. PMID: 35093063 Free PMC article.
References
-
- Hirose S. The causes of underdiagnosing akathisia. Schizophr Bull 2003;29(3):547-58.
-
- Barnes TRE. The Barnes Akathisia rating scale-revisited. J Psychopharmacol (Oxf) 2003;17(4):365-70.
-
- Kane JM, Fleischhacker WW, Hansen L, Perlis R, Pikalov A, Assunção-Talbott S. Akathisia: an updated review focusing on second-generation antipsychotics. J Clin Psychiatry 2009;70(5):627-43.
-
- Putten TV. Why do schizophrenic patients refuse to take their drugs? Arch Gen Psychiatry 1974;31(1):67-72.
-
- Seemüller F, Lewitzka U, Bauer M, et al. The relationship of akathisia with treatment emergent suicidality among patients with first-episode schizophrenia treated with haloperidol or risperidone. Pharmacopsychiatry 2012;45(07):292-6.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials