The provided text consists solely of journal masthead and editorial board information, containing no clinical study data or findings.
Does P2Y12 inhibitor monotherapy reduce bleeding compared to aspirin monotherapy or continued DAPT after PCI?
This review provides clinical guidance on the emerging strategy of P2Y12 inhibitor monotherapy for antiplatelet de-escalation after PCI to reduce bleeding risk.
Antiplatelet therapy is considered essential for secondary prevention of ischemic heart disease. After percutaneous coronary intervention (PCI), temporary dual antiplatelet therapy (DAPT), a combination consisting of aspirin and an oral P2Y12 receptor blocker, is recommended. In the long term, this strategy results in more bleeding than antiplatelet therapy with aspirin alone. Therefore, to reduce bleeding, an increasing trend has been to keep DAPT as short as clinically acceptable, after which aspirin monotherapy is continued. Another option to diminish bleeding is to discontinue aspirin at the moment of DAPT cessation after PCI, and to continue on P2Y12 blocker monotherapy. This survey reviews the evidence on P2Y12 blocker monotherapy. Some clinical guidance will be provided on when and in whom P2Y12 inhibitor monotherapy may be applied after DAPT cessation following PCI.
Verheugt et al. (Fri,) conducted a review in Percutaneous Coronary Intervention. Platelet P2Y12 Inhibitor Monotherapy was evaluated. The provided text consists solely of journal masthead and editorial board information, containing no clinical study data or findings.