Conventional dual antiplatelet therapy (DAPT) for patients with acute coronary syndromes undergoing percutaneous coronary intervention comprises aspirin with a potent P2Y purinoceptor 12 (P2Y 12 ) inhibitor (prasugrel or ticagrelor) for 12 months. Although this approach reduces ischaemic risk, patients are exposed to a substantial risk of bleeding. Strategies to reduce bleeding include de-escalation of DAPT intensity (downgrading from potent P2Y 12 inhibitor at conventional doses to either clopidogrel or reduced-dose prasugrel) or abbreviation of DAPT duration. Either strategy requires assessment of the ischaemic and bleeding risks of each individual. De-escalation of DAPT intensity can reduce bleeding without increasing ischaemic events and can be guided by platelet function testing or genotyping. Abbreviation of DAPT duration after 1-6 months, followed by monotherapy with aspirin or a P2Y 12 inhibitor, reduces bleeding without an increase in ischaemic events in patients at high bleeding risk, particularly those without high ischaemic risk. However, these two strategies have not yet been compared in a head-to-head clinical trial. In this Consensus Statement, we summarize the evidence base for these treatment approaches, provide guidance on the assessment of ischaemic and bleeding risks, and provide consensus statements from an international panel of experts to help clinicians to optimize these DAPT approaches for individual patients to improve outcomes.Sections Although the ARC-HBR criteria and the PRECISE-DAPT Risk Calculator can be adequately applied to real-world cohorts, several important clinical risk factors for bleeding are not covered by these scores (such as low body weight, frailty, heart failure and peripheral artery disease) and, therefore, risk of bleeding might be underestimated in these patients 24 .
Methods for consensus recommendationsWe conducted a search of the literature to identify clinical trials of de-escalation of DAPT intensity or abbreviation of DAPT duration in patients with ACS treated with PCI. The PubMed, Embase and Cochrane Library databases were searched for papers published up to November 2022, with no restriction on language. Reference lists of selected papers were also checked for additional relevant papers. The authors worked on allocated sections of this Consensus Statement in pairs. All the authors reviewed all sections of the manuscript and participated in a series of 'rounds', in which the manuscript was shared with all other authors and the comments made were used to inform and evolve the manuscript in the next round. Video discussions between the authors were also conducted. All the authors judged the available evidence, leading to the consensus recommendations.
Risk of bleeding in clinical trialsIn clinical trials of DAPT, the incidence of major bleeding in the 12 months after PCI among patients with ACS is 1-10% depending Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author...