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Prasugrel-Based De-Escalation in Patients With Acute Coronary Syndrome According to Renal Function
Jun Pil Yun1, Jeehoon Kang1, Kyung Woo Park1
1Seoul National University Hospital, Seoul, Republic of Korea.
Insights
Prasugrel dose de-escalation after percutaneous coronary intervention (PCI) benefits patients with coronary artery disease, irrespective of their renal function. This strategy effectively reduces bleeding risks, particularly in those with impaired kidney function.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Patients with coronary artery disease (CAD) and impaired renal function face elevated risks of bleeding and ischemic events post-percutaneous coronary intervention (PCI).
- Renal function significantly influences the management and outcomes of patients undergoing PCI.
Purpose of the Study:
- To evaluate the efficacy and safety of a prasugrel-based de-escalation strategy in patients with varying degrees of renal function.
- To determine if prasugrel de-escalation impacts bleeding and ischemic outcomes differently across renal function categories.
Main Methods:
- A post hoc analysis of the HOST-REDUCE-POLYTECH-ACS study involving 2,311 patients with available estimated glomerular filtration rate (eGFR).
- Patients were stratified into three groups based on eGFR: high (>90 mL/min), intermediate (60-90 mL/min), and low (<60 mL/min).
- Primary endpoints included bleeding outcomes (BARC type 2 or higher) and ischemic outcomes (cardiovascular death, MI, stent thrombosis, revascularization, ischemic stroke) at 1-year follow-up.
Main Results:
- Prasugrel de-escalation demonstrated benefits across all renal function groups (P interaction = 0.508).
- A higher relative reduction in bleeding risk was observed with prasugrel de-escalation in the low eGFR group (64%) compared to intermediate (50%) and high (52%) eGFR groups.
- No significant increase in ischemic risk was associated with prasugrel de-escalation across any eGFR group (P interaction = 0.119).
Conclusions:
- Prasugrel dose de-escalation is a beneficial strategy for patients with acute coronary syndrome undergoing PCI, regardless of baseline renal function.
- The de-escalation strategy significantly reduces bleeding events, with a more pronounced effect in patients with lower estimated glomerular filtration rates.
Background:
Patients with coronary artery disease and impaired renal function are at higher risk for both bleeding and ischemic adverse events after percutaneous coronary intervention (PCI).
Objectives:
This study assessed the efficacy and safety of a prasugrel-based de-escalation strategy in patients with impaired renal function.
Methods:
We conducted a post hoc analysis of the HOST-REDUCE-POLYTECH-ACS study. Patients with available estimated glomerular filtration rate (eGFR) (n = 2,311) were categorized into 3 groups. (high eGFR: >90 mL/min; intermediate eGFR: 60 to 90 mL/min; and low eGFR: <60 mL/min). The end points were bleeding outcomes (Bleeding Academic Research Consortium type 2 or higher), ischemic outcomes (cardiovascular death, myocardial infarction, stent thrombosis, repeated revascularization, and ischemic stroke), and net adverse clinical event (including any clinical event) at 1-year follow-up.
Results:
Prasugrel de-escalation was beneficial regardless of baseline renal function (P for interaction = 0.508). The relative reduction in bleeding risk from prasugrel de-escalation was higher in the low eGFR group than in both the intermediate and high eGFR groups (relative reductions, respectively: 64% (HR: 0.36; 95% CI: 0.15-0.83) vs 50% (HR: 0.50; 95% CI: 0.28-0.90) and 52% (HR: 0.48; 95% CI: 0.21-1.13) (P for interaction = 0.646). Ischemic risk from prasgurel de-escalation was not significant in all eGFR groups (HR: 1.18 [95% CI: 0.47-2.98], HR: 0.95 [95% CI: 0.53-1.69], and HR: 0.61 [95% CI: 0.26-1.39]) (P for interaction = 0.119).
Conclusions:
In patients with acute coronary syndrome receiving PCI, prasugrel dose de-escalation was beneficial regardless of the baseline renal function.
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