ArticleAmerican heart journal plus : cardiology research and practice2026
Ticagrelor versus prasugrel following PCI in acute coronary syndromes and high-risk coronary artery disease: A meta-analysis of one-year randomized trial outcomes.
Article in American heart journal plus : cardiology research and practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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13 authors.
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Abstract
Background: Guidelines recommend potent P2Y12 inhibitors over clopidogrel following percutaneous coronary intervention. Whether ticagrelor- or prasugrel-based dual antiplatelet therapy (DAPT) provides superior clinical outcomes following percutaneous coronary intervention (PCI) remains uncertain, particularly across acute coronary syndromes (ACS) and high-risk coronary artery disease (CAD) populations. Methods: We searched databases for randomized controlled trials comparing ticagrelor- and prasugrel-based DAPT in patients with CAD undergoing PCI with 1-year follow-up. The primary outcomes were major adverse cardiovascular events (MACE) and all-cause mortality. Secondary outcomes included cardiovascular death, myocardial infarction, stroke, stent thrombosis, and major bleeding. Hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled using random-effects models. Sensitivity analyses were performed in ACS populations. Results: Three trials randomized a total of 7048 patients. In the primary analysis, prasugrel-based therapy was not associated with a statistically significant reduction in MACE compared with ticagrelor-based therapy (HR = 0.83; 95% CI: 0.67-1.03; Conclusions: Among patients with ACS and high-risk CAD undergoing PCI, current randomized evidence does not establish conclusive superiority between ticagrelor- and prasugrel-based DAPT for 1-year ischemic or bleeding endpoints.
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