Key result
Reduced-dose prasugrel lowered the risk of major adverse cardiovascular events compared to standard-dose clopidogrel (OR 0.80) in patients undergoing percutaneous coronary intervention.
Why the study?
Whether reduced-dose prasugrel has better efficacy or safety than standard-dose clopidogrel remains unknown in patients undergoing PCI.
Does reduced-dose prasugrel reduce MACE in patients undergoing percutaneous coronary intervention compared to standard-dose clopidogrel?
Meta-Analysis (n=32,951)
Yes
Does reduced-dose prasugrel reduce MACE in patients undergoing percutaneous coronary intervention compared to standard-dose clopidogrel?
Odds Ratio: 0.8 (95% CI 0.67–0.97)
Reduced-dose prasugrel is associated with a lower risk of MACE but a higher risk of minor bleeding compared to standard-dose clopidogrel in patients undergoing PCI.
Reduced-dose prasugrel was associated with lower MACE but higher minor bleeding in PCI; leaves open confirmation in randomized trials.
Whether reduced-dose prasugrel has a better efficacy or safety than standard-dose clopidogrel remains unknown in patients undergoing percutaneous coronary intervention (PCI).A systematic search of PubMed, EMBASE, Google Scholar, and Cochrane Library from database inception to May 1, 2020 was performed to compare the clinical outcomes in patients with acute coronary syndrome or stable coronary artery disease undergoing PCI between those treated with reduced-dose prasugrel and clopidogrel. The pooled odds ratio (OR) and 95% confidence interval (CI) were calculated using the fixed-effect or random-effect model if significant heterogeneity was observed. The primary efficacy endpoint was major adverse cardiovascular events (MACE), including cardiovascular (CV) death, myocardial infarction (MI), or ischemic stroke. The primary safety endpoint was all bleeding events.Overall, seven studies with 32,951 patients with PCI were included in the analysis. Reduced-dose prasugrel was associated with a lower risk of MACE than clopidogrel (OR 0.80, 95% CI 0.67-0.97). Except for MI (OR 0.74, 95% CI 0.56-0.98), the secondary efficacy endpoints of CV death, ischemic stroke, all-cause death, and stent thrombosis were similar. For the primary safety endpoint of all bleeding events, there was no significant difference between reduced-dose prasugrel and clopidogrel (OR 1.31, 95% CI 0.87-1.98), but the risk of minor bleeding was significantly higher in reduced-dose prasugrel (OR 1.73, 95% CI 1.25-2.41).In patients undergoing PCI, a lower risk of MACE was found in patients receiving reduced-dose prasugrel than in those with clopidogrel, but a higher risk of minor bleeding events was noted.
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Lee et al. (2021) conducted a meta-analysis in Acute coronary syndrome or stable coronary artery disease undergoing percutaneous coronary intervention (n=32,951). Reduced-dose prasugrel vs. Standard-dose clopidogrel was evaluated on Major adverse cardiovascular events (MACE), including cardiovascular death, myocardial infarction, or ischemic stroke (OR 0.80, 95% CI 0.67-0.97). Reduced-dose prasugrel lowered the risk of major adverse cardiovascular events compared to standard-dose clopidogrel (OR 0.80) in patients undergoing percutaneous coronary intervention.
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