Key result
Bivalirudin did not significantly lower the risk of acute kidney injury compared with unfractionated heparin in ACS patients undergoing invasive management (16.9% vs 17.4%; OR 0.97; 95% CI 0.85-1.09).
Why the study?
The impact of adjunctive antithrombotic strategies, such as bivalirudin versus unfractionated heparin, on the risk of acute kidney injury in ACS patients undergoing invasive management was unclear.
Does bivalirudin reduce acute kidney injury in patients with acute coronary syndrome undergoing invasive management compared to unfractionated heparin?
RCT (n=7,085)
Does bivalirudin reduce acute kidney injury in patients with acute coronary syndrome undergoing invasive management compared to unfractionated heparin?
In patients with ACS undergoing invasive management, bivalirudin does not significantly reduce the risk of acute kidney injury compared with unfractionated heparin.
Answers are grounded in this paper and cite their sources.
Bivalirudin confers no AKI advantage over UFH in ACS; confirms equivalent renal safety for periprocedural anticoagulation.
AIMS: Acute kidney injury (AKI) is a critical complication among patients with acute coronary syndrome (ACS) undergoing invasive management. The value of adjunctive antithrombotic strategies, such as bivalirudin or unfractionated heparin (UFH) on the risk of AKI is unclear. METHODS AND RESULTS: Among 7213 patients enrolled in the MATRIX-Antithrombin and Treatment Duration study, 128 subjects were excluded due to incomplete information on serum creatinine (sCr) or end-stage renal disease on dialysis treatment. The primary endpoint was AKI defined as an absolute (>0.5 mg/dL) or a relative (>25%) increase in sCr. AKI occurred in 601 patients (16.9%) treated with bivalirudin and 616 patients (17.4%) treated with UFH [odds ratio (OR): 0.97; 95% confidence interval (CI): 0.85-1.09; P = 0.58]. A >25% sCr increase was observed in 597 patients (16.8%) with bivalirudin and 616 patients (17.4%) with UFH (OR: 0.96; 95% CI: 0.85-1.08; P = 0.50), whereas a >0.5 mg/dL absolute sCr increase occurred in 176 patients (5.0%) with bivalirudin vs. 189 patients (5.4%) with UFH (OR: 0.92; 95% CI: 0.75-1.14; P = 0.46). By implementing the Kidney Disease Improving Global Outcomes (KDIGO) criteria, the risk of AKI was not significantly different between bivalirudin and UFH groups (OR: 0.88; 95% CI: 0.72-1.07; P = 0.21). Subgroup analyses of the primary endpoint suggested a benefit with bivalirudin in patients randomized to femoral access. CONCLUSION: Among ACS patients undergoing invasive management, the risk of AKI was not significantly lower with bivalirudin compared with UFH. TRIAL REGISTRATION: clinicaltrials.gov NCT01433627.
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Landi et al. (2021) conducted an RCT in Acute coronary syndrome (ACS) (n=7,085). Bivalirudin vs. Unfractionated heparin (UFH) was evaluated on Acute kidney injury (AKI) defined as an absolute (>0.5 mg/dL) or a relative (>25%) increase in serum creatinine (OR 0.97, 95% CI 0.85-1.09, p=0.58). Bivalirudin did not significantly lower the risk of acute kidney injury compared with unfractionated heparin in ACS patients undergoing invasive management (16.9% vs 17.4%; OR 0.97; 95% CI 0.85-1.09).
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