Prasugrel use lower in ACS patients with CKD undergoing PCI
American College of Cardiology News Nov 01, 2017
A new analysis has shown that in patients with chronic kidney disease (CKD) and acute coronary syndrome (ACS) undergoing PCI, the use of prasugrel is less frequent than clopidogrel. The study, published October 16, in the journal JACC: Cardiovascular Interventions, also showed the risk for major adverse cardiac events was significantly higher in patients with CKD than without CKD. The findings highlight the need for randomized studies evaluating the ideal antiplatelet therapy in CKD patients with ACS.
Using data from PROMETHEUS, a multicenter observational study comparing outcomes with prasugrel vs. clopidogrel in ACS PCI patients, Usman Baber MD, MS, et al., sought to compare clinical outcomes stratified by CKD status in the 19,832 patients with data on glomerular filtration rates.
The primary endpoint of the main study was 90-day MACE, defined as a composite of death, myocardial infarction (MI), stroke or unplanned revascularization. This analysis considered all clinical endpoints at 90 days and one year. Also evaluated was stent thrombosis and clinically significant bleeding, defined as bleeding requiring hospitalization or transfusion.
CKD was identified in 28.3% of study patients; they were more often women, older, and had more comorbidities, such as diabetes and multivessel disease, and more likely to be treated with bare metal stents and bivalirudin. Prasugrel was prescribed about 50% less frequently to patients with vs. without CKD (11.0% vs 24.0%).
At one year, CKD was associated with a greater risk of MACE and clinically significant bleeding. At 90 days, the adjusted HR was 1.25.
For the individual components of the MACE endpoint, there was a greater risk of MI at one year with CKD. But the risk of unplanned revascularization and stent thrombosis was similar regardless of CKD status.
The study authors note their observations also fit with existing literature on higher bleeding risk in CKD patients. "This may be the result of ineffective platelets, anemia and thrombocytopenia in this mostly elderly and female patient population," the authors write. "Interestingly, assessment of platelet reactivity may allow balanced selection of CKD patients at greater ischemic risk who may benefit from potent therapies such as prasugrel without the tradeoff of greater bleeding."
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Using data from PROMETHEUS, a multicenter observational study comparing outcomes with prasugrel vs. clopidogrel in ACS PCI patients, Usman Baber MD, MS, et al., sought to compare clinical outcomes stratified by CKD status in the 19,832 patients with data on glomerular filtration rates.
The primary endpoint of the main study was 90-day MACE, defined as a composite of death, myocardial infarction (MI), stroke or unplanned revascularization. This analysis considered all clinical endpoints at 90 days and one year. Also evaluated was stent thrombosis and clinically significant bleeding, defined as bleeding requiring hospitalization or transfusion.
CKD was identified in 28.3% of study patients; they were more often women, older, and had more comorbidities, such as diabetes and multivessel disease, and more likely to be treated with bare metal stents and bivalirudin. Prasugrel was prescribed about 50% less frequently to patients with vs. without CKD (11.0% vs 24.0%).
At one year, CKD was associated with a greater risk of MACE and clinically significant bleeding. At 90 days, the adjusted HR was 1.25.
For the individual components of the MACE endpoint, there was a greater risk of MI at one year with CKD. But the risk of unplanned revascularization and stent thrombosis was similar regardless of CKD status.
The study authors note their observations also fit with existing literature on higher bleeding risk in CKD patients. "This may be the result of ineffective platelets, anemia and thrombocytopenia in this mostly elderly and female patient population," the authors write. "Interestingly, assessment of platelet reactivity may allow balanced selection of CKD patients at greater ischemic risk who may benefit from potent therapies such as prasugrel without the tradeoff of greater bleeding."
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