Key result
Bupropion and varenicline use for smoking cessation were not associated with increased risk of acute myocardial infarction.
Why the study?
Does bupropion or varenicline increase the risk of acute cardiovascular events and injuries in adults?
Observational
Yes
Does bupropion or varenicline increase the risk of acute cardiovascular events and injuries in adults?
Bupropion and varenicline used for smoking cessation do not appear to increase the short-term risk of acute cardiovascular events, suicide, or injuries.
Answers are grounded in this paper and cite their sources.
Supports no AMI risk increase with bupropion or varenicline; leaves open causal confirmation from randomized trials.
Introduction: Bupropion and varenicline are non-nicotine medications used for smoking cessation that mitigate craving and withdrawal symptoms. We aim to investigate whether these drugs increase the risk of selected acute adverse outcomes when used in medical practice. Methods: Population-based case-crossover design using data from Swedish health and administrative registers. Adult individuals diagnosed with acute myocardial infarction, stroke, suicide, suicide attempt, fall injury, or that suffered a road traffic crash from 01.10.2006 for bupropion, or from 01.03.2008 for varenicline, until 31.12.2013 were included. Different lengths of exposure periods were analyzed within the 12-week hazard period prior to the adverse outcome (1-14, 15-28, and 29-84 days). The control period was matched using the interval preceding the hazard period (85-168 days), and breaking it up into equivalent periods (85-98, 99-112, and 113-168 days). Conditional logistic regression with each case considered as one stratum was used to estimate adjusted odds ratios (OR) and confidence intervals (CI). Results: Neither medication was associated with consistent higher risks for any of the adverse outcomes. For bupropion and varenicline, respectively, in the 1-14 days hazard period, OR (95% CI) were: myocardial infarction 1.14 (0.55 to 2.34) and 1.06 (0.70 to 1.62); stroke 1.16 (0.39 to 3.47) and 1.26 (0.72 to 2.17), and traffic crashes 0.85 (0.39 to 1.85) and 1.48 (0.90 to 2.41). In the other periods, ORs were similar or even lower. For falls and suicidal events ORs were generally below one for both drugs. Conclusion: The available evidence suggests that if prescription guidelines are properly followed regarding potential contraindications both of these medications could be considered relatively safe. Implications: The reliable exposure and diagnosis assessment used in this nationwide register-based study, along with the number of cases gathered makes this sample one of the largest of its type to assess potential side effects associated with the use of these drugs. Neither medication was associated with consistent higher risks for any of the adverse outcomes studied.
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Monárrez‐Espino et al. (2017) conducted an observational in Smoking cessation. Bupropion and varenicline vs. Interval preceding the hazard period (85-168 days prior) was evaluated on Acute myocardial infarction, stroke, suicide, suicide attempt, fall injury, or road traffic crash (OR 1.14, 95% CI 0.55-2.34). Bupropion and varenicline use for smoking cessation were not associated with increased risk of acute myocardial infarction.
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