Key result
Ticagrelor-based DAPT after CABG is linked to ~2.1-fold higher all-cause mortality versus aspirin.
Why the study?
Although aspirin is universally recommended after CABG, the incremental benefit of ticagrelor-based DAPT remained uncertain, with persistent concerns regarding bleeding risk and inconsistent clinical outcomes.
Does ticagrelor-based dual antiplatelet therapy reduce all-cause mortality and bleeding compared to aspirin monotherapy in patients undergoing CABG for ACS or stable CAD?
Meta-Analysis (n=3,101)
Does ticagrelor-based dual antiplatelet therapy reduce all-cause mortality and bleeding compared to aspirin monotherapy in patients undergoing CABG for ACS or stable CAD?
In patients undergoing CABG, routine ticagrelor-based dual antiplatelet therapy is associated with significantly higher risks of all-cause mortality and both major and minor bleeding compared to aspirin monotherapy.
Answers are grounded in this paper and cite their sources.
Ticagrelor-based DAPT should be avoided post-CABG; challenges dual therapy recommendations in this population.
Background Antiplatelet therapy after coronary artery bypass grafting (CABG) plays a central role in preventing graft thrombosis and reducing adverse cardiovascular events. Aspirin is universally recommended as the cornerstone of postoperative antiplatelet therapy; however, the incremental benefit of dual antiplatelet therapy (DAPT) with ticagrelor remains uncertain. While some trials have suggested potential improvements in graft patency, concerns persist regarding bleeding risk and the lack of consistent benefit on clinical outcomes. Purpose To systematically evaluate the efficacy and safety of ticagrelor-based DAPT following CABG in patients with acute coronary syndrome (ACS) or stable coronary artery disease (CAD). Methods We conducted a systematic search of Embase, MEDLINE, and Cochrane databases from inception to December 2025 to identify randomized controlled trials (RCTs) comparing ticagrelor plus aspirin versus aspirin monotherapy in patients undergoing CABG for ACS or stable CAD. Binary outcomes were pooled as risk ratios (RR) with 95% confidence intervals (CI) using a Mantel–Haenszel common-effect model, while continuous outcomes were summarized as mean differences (MD). Heterogeneity was assessed using Cochrane’s Q test and Higgins and Thompson’s I² statistic. All analyses were performed using R software (version 4.4.2). Results Following PRISMA guidelines, 2,573 records were screened, and 4 RCTs comprising 3,101 patients were included, of whom 50.1% were allocated to ticagrelor-based DAPT. Using a common-effect model, ticagrelor-based DAPT was associated with a significantly higher risk of all-cause mortality over a follow-up ranging from 1 to 5 years compared with aspirin monotherapy (RR 2.15; 95% CI 1.17–3.94; p = 0.013), with moderate heterogeneity across studies (I² < 50%). At 1 year, DAPT was also associated with significantly increased risks of major bleeding (RR 2.10; 95% CI 1.37–3.21; p < 0.001) and minor bleeding (RR 2.92; 95% CI 1.72–4.96; p < 0.001), both with moderate heterogeneity (I² < 50%). Conclusion In patients undergoing CABG, ticagrelor-based dual antiplatelet therapy was associated with higher risks of all-cause mortality and bleeding. These findings highlight important safety concerns regarding the routine use of ticagrelor-based DAPT after CABG and support a cautious, individualized approach to postoperative antiplatelet management.Major and minor bleending after 1 year.All-cause mortality after 1-5 years.
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Goes et al. (2026) conducted a meta-analysis in Acute coronary syndrome or stable coronary artery disease undergoing coronary artery bypass grafting (n=3,101). Ticagrelor-based dual antiplatelet therapy (ticagrelor plus aspirin) vs. Aspirin monotherapy was evaluated on All-cause mortality (RR 2.15, 95% CI 1.17-3.94, p=0.013). Ticagrelor-based DAPT after CABG was associated with higher all-cause mortality vs aspirin alone (RR 2.15; 95% CI 1.17-3.94; p=0.013) and major bleeding (RR 2.10; 95% CI 1.37-3.21; p<0.001).
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