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Assessment of Switching to Suvorexant versus the Use of Add-on Suvorexant in Combination with Benzodiazepine Receptor Agonists in Insomnia Patients: A Retrospective Study.
Hatano, Masakazu; Kamei, Hiroyuki; Inagaki, Risa; Matsuzaki, Haruna; Hanya, Manako; Yamada, Shigeki; Iwata, Nakao.
Afiliação
  • Hatano M; Department of Psychiatry, Fujita Health University School of Medicine, Aichi, Japan.
  • Kamei H; Department of Clinical Pharmacy, Fujita Health University School of Medicine, Aichi, Japan.
  • Inagaki R; Office of Clinical Pharmacy Practice and Health Care Management, Faculty of Pharmacy, Meijo University, Nagoya, Japan.
  • Matsuzaki H; Office of Clinical Pharmacy Practice and Health Care Management, Faculty of Pharmacy, Meijo University, Nagoya, Japan.
  • Hanya M; Department of Clinical Pharmacy, Fujita Health University School of Medicine, Aichi, Japan.
  • Yamada S; Department of Clinical Pharmacy, Fujita Health University School of Medicine, Aichi, Japan.
  • Iwata N; Office of Clinical Pharmacy Practice and Health Care Management, Faculty of Pharmacy, Meijo University, Nagoya, Japan.
Clin Psychopharmacol Neurosci ; 16(2): 184-189, 2018 May 31.
Article em En | MEDLINE | ID: mdl-29739132
ABSTRACT

OBJECTIVE:

Suvorexant is a novel hypnotic drug that does not interact with the conventional γ-aminobutyric acid (GABA)-A receptor. We investigated the method by which suvorexant was introduced in insomnia patients who were taking benzodiazepine receptor agonists (BzRA).

METHODS:

This was a retrospective study. We extracted clinical data for patients who were prescribed suvorexant and were already using BzRA. The patients were assigned to two groups, the switching and add-on groups. We assessed the suvorexant discontinuation rate at one month after the prescription of the drug.

RESULTS:

One hundred and nineteen patients were assigned to the switching group, and 109 were assigned to the add-on group. The add-on group exhibited a significantly higher all-cause discontinuation rate than the switching group (odds ratio, 2.7; 95% confidence interval, 1.5 to 5.0; adjusted p<0.001). Intolerability was a significantly stronger risk factor for suvorexant discontinuation in the add-on group (22.0% vs. 7.6%, p<0.002), and the most common adverse effect was oversedation.

CONCLUSION:

Our results show that the add-on of suvorexant increases the frequency of oversedation compared with switching in insomnia patients that are taking BzRA. However, this was only a preliminary retrospective study, and further studies will be required to confirm our findings.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article