Why the study?
To evaluate potentially appropriate antiplatelet therapy regimens with enhanced platelet inhibition activity compared to standard clopidogrel-based DAPT in patients with chronic kidney disease.
Do antiplatelet therapy regimens with enhanced platelet inhibition activity improve net clinical benefit compared to standard dose clopidogrel-based dual antiplatelet therapy in patients with chronic kidney disease and acute coronary syndrome?
Do antiplatelet therapy regimens with enhanced platelet inhibition activity improve net clinical benefit compared to standard dose clopidogrel-based dual antiplatelet therapy in patients with chronic kidney disease and acute coronary syndrome?
Enhanced antiplatelet therapy improves clinical outcomes in patients with mild-to-moderate renal insufficiency and ACS, but standard clopidogrel is favorable for those with severe renal insufficiency due to elevated bleeding risk.
Potent P2Y12 regimens may improve outcomes in moderate CKD-ACS; extends meta-analytic evidence while cautioning against use in severe renal impairment.
This study aims to evaluate potentially appropriate antiplatelet therapy in patients with chronic kidney disease. A systematic analysis was conducted to identify the clinical outcomes of available antiplatelet therapy regimens with enhanced platelet inhibition activity (intervention of 5 regimens) over the standard dose of clopidogrel-based dual antiplatelet therapy in patients with renal insufficiency. An electronic keyword search was performed on Pubmed, Embase, and Cochrane Library per PRISMA guidelines. We performed a prespecified net clinical benefit analysis (a composite of the rates of all-cause or cardiac-related death, myocardial infarction, major adverse cardiac outcomes, and minor and major bleeding), and included 12 studies. The intervention substantially lowered the incidence of all-cause mortality (RR 0.67; p = 0.003), major adverse cardiac outcomes (RR 0.79; p < 0.00001), and myocardial infarction (RR 0.28; p = 0.00007) without major bleeding (RR 1.14; p = 0.33) in patients with renal insufficiency, but no significant differences were noticed with cardiac-related mortality and stent thrombosis. The subgroup analysis revealed substantially elevated bleeding risk in patients with severe renal insufficiency or on hemodialysis (RR 1.68; p = 0.002). Our study confirmed that the intervention considerably enhances clinical outcomes in patients with renal insufficiency, however, a standard dose of clopidogrel-based antiplatelet therapy is favorable in patients with severe renal insufficiency.
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Park et al. (2021) studied this question.
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