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Suvorexant for the treatment of primary insomnia: A systematic review and meta-analysis.
Sleep Med Rev. 2017 Oct; 35:1-7.SM

Abstract

Suvorexant is a dual orexin receptor agonist and is currently approved for the treatment of insomnia in the United States and Japan. We conducted a systematic review and meta-analysis to assess the efficacy and safety of suvorexant for the treatment of primary insomnia. We searched PubMed, EMBASE, and the Cochrane central register of controlled trials, contacted a relevant pharmaceutical company, and accessed websites of the U.S. Food and Drug Administration (FDA) and Pharmaceuticals and Medical Devices Agency (PMDA) for published and unpublished data. A total of four randomized trials involving 3076 patients with primary insomnia were included in our analysis. Our analysis suggested that suvorexant was associated with significant improvements in subjective time to sleep onset, subjective total sleep time, and subjective quality of sleep at 1 mo and 3 mo. Somnolence, fatigue, and abnormal dreams were the most common adverse effects. We concluded that suvorexant was associated with improvement in some sleep parameters and some adverse effects. To determine the place of suvorexant in the treatment of insomnia, comparative effectiveness trials are needed.

Authors+Show Affiliations

Department of General Medicine, Kurashiki Central Hospital, 1-1-1 Miwa, Kurashiki, Okayama 710-8602, Japan. Electronic address: akira.kuriyama.jpn@gmail.com.Department of Neurology, Kurashiki Central Hospital, Japan.

Pub Type(s)

Journal Article
Meta-Analysis
Systematic Review

Language

eng

PubMed ID

28365447

Citation

Kuriyama, Akira, and Hiromitsu Tabata. "Suvorexant for the Treatment of Primary Insomnia: a Systematic Review and Meta-analysis." Sleep Medicine Reviews, vol. 35, 2017, pp. 1-7.
Kuriyama A, Tabata H. Suvorexant for the treatment of primary insomnia: A systematic review and meta-analysis. Sleep Med Rev. 2017;35:1-7.
Kuriyama, A., & Tabata, H. (2017). Suvorexant for the treatment of primary insomnia: A systematic review and meta-analysis. Sleep Medicine Reviews, 35, 1-7. https://doi.org/10.1016/j.smrv.2016.09.004
Kuriyama A, Tabata H. Suvorexant for the Treatment of Primary Insomnia: a Systematic Review and Meta-analysis. Sleep Med Rev. 2017;35:1-7. PubMed PMID: 28365447.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Suvorexant for the treatment of primary insomnia: A systematic review and meta-analysis. AU - Kuriyama,Akira, AU - Tabata,Hiromitsu, Y1 - 2016/10/28/ PY - 2016/6/1/received PY - 2016/9/16/revised PY - 2016/9/19/accepted PY - 2017/4/4/pubmed PY - 2018/6/5/medline PY - 2017/4/3/entrez KW - Abnormal dreams KW - Belsomra KW - Insomnia KW - Meta-analysis KW - Primary insomnia KW - REM sleep behavior disorder KW - Randomized controlled trials KW - Suvorexant KW - Systematic review SP - 1 EP - 7 JF - Sleep medicine reviews JO - Sleep Med Rev VL - 35 N2 - Suvorexant is a dual orexin receptor agonist and is currently approved for the treatment of insomnia in the United States and Japan. We conducted a systematic review and meta-analysis to assess the efficacy and safety of suvorexant for the treatment of primary insomnia. We searched PubMed, EMBASE, and the Cochrane central register of controlled trials, contacted a relevant pharmaceutical company, and accessed websites of the U.S. Food and Drug Administration (FDA) and Pharmaceuticals and Medical Devices Agency (PMDA) for published and unpublished data. A total of four randomized trials involving 3076 patients with primary insomnia were included in our analysis. Our analysis suggested that suvorexant was associated with significant improvements in subjective time to sleep onset, subjective total sleep time, and subjective quality of sleep at 1 mo and 3 mo. Somnolence, fatigue, and abnormal dreams were the most common adverse effects. We concluded that suvorexant was associated with improvement in some sleep parameters and some adverse effects. To determine the place of suvorexant in the treatment of insomnia, comparative effectiveness trials are needed. SN - 1532-2955 UR - https://www.unboundmedicine.com/medline/citation/28365447/full_citation DB - PRIME DP - Unbound Medicine ER -