Key result
Ticagrelor and prasugrel demonstrate similar all-cause mortality in ACS patients undergoing PCI.
Why the study?
Does ticagrelor improve all-cause mortality compared to prasugrel in patients with acute coronary syndrome undergoing percutaneous coronary intervention?
Meta-Analysis
Does ticagrelor improve all-cause mortality compared to prasugrel in patients with acute coronary syndrome undergoing percutaneous coronary intervention?
Ticagrelor and prasugrel show similar efficacy and safety in ACS patients undergoing PCI, supporting individualized P2Y12 inhibitor selection rather than a strict preference for either agent.
Answers are grounded in this paper and cite their sources.
Supports equivalent prasugrel or ticagrelor use in ACS-PCI; leaves open optimal selection in broader populations.
Acute coronary syndrome remains a prominent cause of morbidity and mortality worldwide despite advances in percutaneous coronary intervention and pharmaceuticals. As such, the discovery and implementation of novel and safe preventative measures like ticagrelor and prasugrel need to be studied and their safety profiles compared. For this purpose, we compiled 3 randomized controlled trials and 1 post hoc study from PubMed, Web of Science, and Cochrane Central after thorough screening, in this meta-analysis. The primary outcome was all-cause mortality. Secondary outcomes included cardiovascular death, myocardial infarction, composite ischemic events, stent thrombosis, stroke, and bleeding events. Prasugrel and ticagrelor demonstrated similar efficacy and safety in patients with acute coronary syndrome undergoing percutaneous coronary intervention. These findings support an individualized approach to P2Y12 inhibitor selection based on patient characteristics, contraindications, tolerability, and adherence considerations rather than a preference for either agent.
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Shafiq et al. (2026) conducted a meta-analysis in Acute coronary syndrome. Ticagrelor vs. Prasugrel was evaluated on All-cause mortality. Ticagrelor and prasugrel demonstrated similar efficacy and safety for all-cause mortality in patients with acute coronary syndrome undergoing percutaneous coronary intervention.
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