Abstract
OBJECTIVE: To determine the risk of neuropsychiatric adverse events associated with use of varenicline compared with placebo in randomised controlled trials.
DESIGN: Systematic review and meta-analysis comparing study effects using two summary estimates in fixed effects models, risk differences, and Peto odds ratios.
DATA SOURCES: Medline, Embase, PsycINFO, the Cochrane Central Register of Controlled Trials (CENTRAL), and clinicaltrials.gov.
ELIGIBILITY CRITERIA FOR SELECTING STUDIES: Randomised controlled trials with a placebo comparison group that reported on neuropsychiatric adverse events (depression, suicidal ideation, suicide attempt, suicide, insomnia, sleep disorders, abnormal dreams, somnolence, fatigue, anxiety) and death. Studies that did not involve human participants, did not use the maximum recommended dose of varenicline (1 mg twice daily), and were cross over trials were excluded.
RESULTS: In the 39 randomised controlled trials (10 761 participants), there was no evidence of an increased risk of suicide or attempted suicide (odds ratio 1.67, 95% confidence interval 0.33 to 8.57), suicidal ideation (0.58, 0.28 to 1.20), depression (0.96, 0.75 to 1.22), irritability (0.98, 0.81 to 1.17), aggression (0.91, 0.52 to 1.59), or death (1.05, 0.47 to 2.38) in the varenicline users compared with placebo users. Varenicline was associated with an increased risk of sleep disorders (1.63, 1.29 to 2.07), insomnia (1.56, 1.36 to 1.78), abnormal dreams (2.38, 2.05 to 2.77), and fatigue (1.28, 1.06 to 1.55) but a reduced risk of anxiety (0.75, 0.61 to 0.93). Similar findings were observed when risk differences were reported. There was no evidence for a variation in depression and suicidal ideation by age group, sex, ethnicity, smoking status, presence or absence of psychiatric illness, and type of study sponsor (that is, pharmaceutical industry or other).
CONCLUSIONS: This meta-analysis found no evidence of an increased risk of suicide or attempted suicide, suicidal ideation, depression, or death with varenicline. These findings provide some reassurance for users and prescribers regarding the neuropsychiatric safety of varenicline. There was evidence that varenicline was associated with a higher risk of sleep problems such as insomnia and abnormal dreams. These side effects, however, : are already well recognised.
SYSTEMATIC REVIEW REGISTRATION: PROSPERO 2014:CRD42014009224.
Original language | English |
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Article number | h1109 |
Number of pages | 11 |
Journal | BMJ |
Volume | 350 |
DOIs | |
Publication status | Published - 12 Mar 2015 |
Bibliographical note
© Thomas et al 2015.Article accepted 2nd February 2015
Research Groups and Themes
- SASH
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Dr Duleeka Knipe
- Bristol Medical School (PHS) - Associate Professor in Global Mental Health
- Bristol Poverty Institute
- Migration Mobilities Bristol
- Bristol Population Health Science Institute
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Professor Kyla H Thomas
- Bristol Medical School (PHS) - Professor of Public Health Medicine
- Bristol Population Health Science Institute
- Centre for Academic Mental Health
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