Pharmacopsychiatry
DOI: 10.1055/a-2331-2300
Original Paper

Discontinuation Rate of Lurasidone and Quetiapine Extended Release in Bipolar Depression

Taro Kishi
1   Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan
,
Kenji Sakuma
1   Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan
,
Shun Hamanaka
1   Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan
,
Yasufumi Nishii
1   Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan
,
Nakao Iwata
1   Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan
› Author Affiliations
Funding This study was supported by JSPS KAKENHI (grant number 23K06998).

Abstract

Introduction Lurasidone (LUR) was compared with quetiapine extended release (QUE-ER) regarding 1-year discontinuation in patients with bipolar depression (n=317).

Methods This is a retrospective cohort study.

Results Although the time to all-cause discontinuation was estimated using the Kaplan–Meier survival curve with log-rank tests to compare treatment groups, no difference was found (p=0.317). The Cox proportional hazard model revealed that only the presence of adverse events (AEs) is associated with increased treatment discontinuation (p<0.0001). The most common AEs were akathisia for LUR (17.7%) and somnolence for QUE-ER (34.7%). In other Cox models divided by LUR or QUE-ER, the presence of akathisia or somnolence was associated with increased LUR (p=0.0205) or QUE-ER (p<0.0001) discontinuation, respectively.

Discussion The acceptability of both antipsychotics to bipolar depression in clinical practice may be similar. However, specific AEs for each antipsychotic (LUR: akathisia and QUE-ER: somnolence) were associated with high treatment discontinuation.

Supplementary Material



Publication History

Received: 06 March 2024
Received: 11 April 2024

Accepted: 13 May 2024

Article published online:
19 June 2024

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