Background: Patients with cancer undergoing percutaneous coronary intervention (PCI) experience higher risk of both ischemic and bleeding events. The aim of this study is to assess ischemic and bleeding risks after PCI in cancer patients treated with potent P2Y12 inhibitors (P2Y12i; prasugrel and ticagrelor), compared to clopidogrel.
Methods: Consecutive cancer patients undergoing PCI at a tertiary centre between 2012 and 2022 and discharged on P2Y12i were included. Propensity score covariate adjustment was used to account for baseline differences between patients treated with potent P2Y12i and clopidogrel. Key clinical endpoints included major adverse cardiac and cerebrovascular events (MACCE - composite of death, myocardial infarction or stroke) and major bleeding.
Results: Of the 1,702 included patients, 373 (21.9%) were treated with potent P2Y12i and 1,329 (78.1%) with clopidogrel. Factors associated with potent P2Y12i use were acute coronary syndrome presentation and lesion length, while clopidogrel use was associated with active cancer status, thrombocytopenia, older age and femoral access. MACCE at one year occurred in 3.5% of patients treated with potent P2Y12i vs. 6.8% of those receiving clopidogrel (log-rank p=0.035; adj. HR: 0.53, 95% CI: 0.26-1.10), while no differences in bleeding risk were detected (5.5% vs. 7.0%, adj. HR: 0.92, 95% CI: 0.53 - 1.60). The reduction in MACCE was significant in patients with remission but not active cancer (p-interaction = 0.011).
Conclusions: Among cancer patients undergoing PCI, potent P2Y12i were associated with similar bleeding risk and lower incidence of ischemic events compared to clopidogrel, however with no significant difference after propensity score adjustment.
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http://dx.doi.org/10.1016/j.cjca.2025.02.035 | DOI Listing |
Can J Cardiol
March 2025
Mount Sinai Fuster Heart Hospital, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Background: Patients with cancer undergoing percutaneous coronary intervention (PCI) experience higher risk of both ischemic and bleeding events. The aim of this study is to assess ischemic and bleeding risks after PCI in cancer patients treated with potent P2Y12 inhibitors (P2Y12i; prasugrel and ticagrelor), compared to clopidogrel.
Methods: Consecutive cancer patients undergoing PCI at a tertiary centre between 2012 and 2022 and discharged on P2Y12i were included.
J Family Med Prim Care
June 2024
Department of Cardiology, King George's Medical University, Lucknow, Uttar Pradesh, India.
Clopidogrel is the most widely used P2Y12 receptor inhibitor (P2Y12i) as a part of dual antiplatelet therapy along with aspirin. Clopidogrel is a pro-drug and is metabolized to its active metabolite by the hepatic enzyme cytochrome P4502C19 (CYP2C19). This active metabolite is responsible for the antiplatelet action of clopidogrel.
View Article and Find Full Text PDFKidney360
August 2022
Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Background: Individuals aged ≥75 years are the fastest-growing population starting dialysis for end-stage kidney disease (ESKD) due to living longer with coronary artery disease. ESKD alone can increase bleeding risk, but P2Y inhibitor (P2Y12-I) antiplatelet medications prescribed for cardiovascular treatment can exacerbate this risk in patients with ESKD. The age-specific rates of bleeding complications in dialysis patients with ESKD on P2Y12-I remain unclear, as does how age modifies the bleeding risk from P2Y12-I use in these patients.
View Article and Find Full Text PDFRev Cardiovasc Med
March 2022
Department of Cardiology, AHEPA University Hospital, 54621 Thessaloniki, Greece.
Background: Superiority of potent P2Y12 inhibitors over clopidogrel after an acute coronary syndrome (ACS) has been well established, however potent P2Y12 inhibition is responsible for more adverse events, which may influence patient adherence to treatment. Aim of the present study is to investigate the adherence to the prescribed P2Y12 inhibitor (P2Y12i) in patients on dual antiplatelet therapy (DAPT) after an ACS.
Methods: In an IDEAL-LDL trial substudy, we included 344 patients after ACS discharged on DAPT.
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