Key result
Postdischarge varenicline shows no benefit over NRT patches for recurrent major cardiovascular events.
Why the study?
The comparative effectiveness of postdischarge varenicline versus prescription nicotine replacement therapy patches for preventing recurrent cardiovascular events and mortality, and whether outcomes differ by sex, was undetermined.
Does varenicline prevent recurrent major cardiovascular events compared to prescription nicotine patches in patients recently hospitalized for a major cardiovascular event?
Cohort (n=3,290)
Does varenicline prevent recurrent major cardiovascular events compared to prescription nicotine patches in patients recently hospitalized for a major cardiovascular event?
Varenicline and prescription nicotine patches have similar effectiveness in preventing recurrent major cardiovascular events when used post-discharge.
Answers are grounded in this paper and cite their sources.
No difference in postdischarge MACE risk with varenicline versus NRT; leaves open whether either improves cessation without excess events in this population.
OBJECTIVE: To determine the comparative effectiveness of postdischarge use of varenicline versus prescription nicotine replacement therapy (NRT) patches for the prevention of recurrent cardiovascular events and mortality and whether this association differs by sex. METHODS: Our cohort study used routinely collected hospital, pharmaceutical dispensing and mortality data for residents of New South Wales, Australia. We included patients hospitalised for a major cardiovascular event or procedure 2011-2017, who were dispensed varenicline or prescription NRT patches within 90day postdischarge. Exposure was defined using an approach analogous to intention to treat. Using inverse probability of treatment weighting with propensity scores to account for confounding, we estimated adjusted HRs for major cardiovascular events (MACEs), overall and by sex. We fitted an additional model with a sex-treatment interaction term to determine if treatment effects differed between males and females. RESULTS: Our cohort of 844 varenicline users (72% male, 75% <65 years) and 2446 prescription NRT patch users (67% male, 65% <65 years) were followed for a median of 2.93 years and 2.34 years, respectively. After weighting, there was no difference in risk of MACE for varenicline relative to prescription NRT patches (aHR 0.99, 95% CI 0.82 to 1.19). We found no difference (interaction p=0.098) between males (aHR 0.92, 95% CI 0.73 to 1.16) and females (aHR 1.30, 95% CI 0.92 to 1.84), although the effect among females deviated from the null. CONCLUSION: We found no difference between varenicline and prescription NRT patches in the risk of recurrent MACE. These results should be considered when determining the most appropriate choice of smoking cessation pharmacotherapy.
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Robijn et al. (2023) conducted a cohort in Hospitalised for a major cardiovascular event or procedure (n=3,290). Varenicline vs. Prescription nicotine replacement therapy (NRT) patches was evaluated on Major cardiovascular events (MACEs) (aHR 0.99, 95% CI 0.82 to 1.19). Postdischarge use of varenicline showed no difference in the risk of recurrent major cardiovascular events compared to prescription NRT patches.
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