Bivalirudin for primary percutaneous coronary interventions: outcome assessment in the Ottawa STEMI registry
Registry study published in Circulation Cardiovascular Interventions (2012)
Abstract
BACKGROUND: Data from randomized trials has demonstrated the superiority of bivalirudin to glycoprotein IIb/IIIa inhibitors plus heparin in patients undergoing primary percutaneous coronary intervention. Real-world performance of bivalirudin in primary percutaneous coronary intervention and the benefit of bivalirudin over heparin remain unknown in an era of routine dual antiplatelet therapy. METHODS AND RESULTS: From July 2004 to December 2010, 2317 consecutive patients were indexed in the University of Ottawa Heart Institute ST-segment-elevation myocardial infarction registry. During this period 748 patients received bivalirudin, 699 patients received glycoprotein IIb/IIIa inhibitors, and 676 patients received unfractionated heparin alone. The primary outcome was the rate of noncoronary artery bypass graft related thrombolysis in myocardial infarction major bleeding. Bivalirudin significantly reduced the primary outcome compared with heparin plus glycoprotein IIb/IIIa inhibitors (2.7% versus 7.3%, adjusted OR 2.96, 95% CI: 1.61-5.45, P<0.001) and the composite end point of death, stroke, reinfarction and major bleed (OR 1.66, 95% CI: 1.12-2.45, P=0.01). Compared with heparin alone, a reduction in major bleeds (OR 1.21, 95% CI: 0.60-2.44, P=0.59) or the composite end point (1.05, 95% CI: 0.68-1.63, P=0.83) with bivalirudin could not be demonstrated. Notably, major bleeding was associated with a 5-fold increase in the risk of mortality both in-hospital (3.5% versus 20.6%) and out to 180 days (5.6% versus 25.8%). CONCLUSIONS: Bivalirudin use compared with glycoprotein IIb/IIIa inhibitors plus heparin as an antithrombotic strategy in primary percutaneous coronary intervention results in less major bleeding in contemporary practice. A benefit of bivalirudin over heparin could not be established with this registry and requires additional investigations to either confirm or refute.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
Ottawa STEMI registry of 2317 patients comparing bivalirudin (n=748) vs heparin+GPI (n=699) vs heparin alone (n=676): bivalirudin reduced TIMI major bleeding (2.7% vs 7.3%, OR 2.96, p<0.001) and the composite end point of death, stroke, reinfarction, major bleed.
Warum dies für die Hirudotherapie relevant ist
This registry analysis of 2,317 consecutive STEMI patients found that bivalirudin significantly reduced major bleeding versus heparin plus glycoprotein IIb/IIIa inhibitors (2.7% vs 7.3%), but no benefit over heparin alone could be demonstrated. The abstract does not mention hirudin, leeches, leech saliva, or any molecular or pharmacological relationship between bivalirudin and leech-derived compounds. No defensible connection to hirudotherapy, the leech secretome, or ASH's domain exists from this abstract alone; the study is a cardiovascular outcomes registry comparing pharmaceutical anticoagulation strategies with no leech involvement whatsoever.
Zitation
Bivalirudin for primary percutaneous coronary interventions: outcome assessment in the Ottawa STEMI registry.
Hibbert B et al. · Circulation Cardiovascular Interventions, 2012
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