Key result
In patients with stable coronary artery disease who completed 6 months of DAPT, a novel risk score identified an upper risk stratum where extending DAPT to 12 months reduced the absolute risk of composite ischemic and bleeding events by 4.8%.
Why the study?
Decisions on DAPT duration must balance the opposing risks of ischaemia and bleeding in patients undergoing PCI for stable coronary artery disease.
Does extending dual antiplatelet therapy beyond 6 months reduce ischemic events without increasing bleeding in patients with stable coronary artery disease post-PCI?
Cohort (n=2,699)
No
Does extending dual antiplatelet therapy beyond 6 months reduce ischemic events without increasing bleeding in patients with stable coronary artery disease post-PCI?
A novel clinical risk score can effectively identify patients with stable coronary artery disease who will benefit from extending dual antiplatelet therapy beyond 6 months post-PCI by balancing ischemic and bleeding risks.
Answers are grounded in this paper and cite their sources.
May support risk-stratified DAPT extension in stable CAD; leaves open randomized validation before practice change.
Decisions on dual antiplatelet therapy (DAPT) duration should balance the opposing risks of ischaemia and bleeding. Our aim was to develop a risk score to identify stable coronary artery disease (SCAD) patients undergoing PCI who would benefit or suffer from extending DAPT beyond 6 months.
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Witberg et al. (2019) conducted a cohort in Stable coronary artery disease (SCAD) post-percutaneous coronary intervention (PCI) (n=2,699). Extended dual antiplatelet therapy (DAPT) vs. 6 months of DAPT was evaluated on Composite of ischaemic and major bleeding events in the upper risk quartile (Q4) (ARR 4.8%, 95% CI -11.6 to 2.0). In patients with stable coronary artery disease who completed 6 months of DAPT, a novel risk score identified an upper risk stratum where extending DAPT to 12 months reduced the absolute risk of composite ischemic and bleeding events by 4.8%.
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