Two hour bivalirudin infusion after PCI for ST elevation myocardial infarction
Multicenter prospective registry published in Journal of Thrombosis and Thrombolysis (2011)
Abstract
The standard of care for STEMI PCI for the past decade has been aspirin, clopidogrel, heparin, and a glycoprotein IIbIIIa receptor inhibitor (GPI). A bivalirudin strategy was shown to be superior to a GPI strategy in the HORIZONS AMI trial for net adverse clinical events (combined MACE and bleeding). An increased risk of acute stent thrombosis in the bivalirudin arm may have prevented broader adoption of bivalirudin for this indication. We hypothesized that acute stent thrombosis risk could be ameliorated by a 2 h infusion of bivalirudin following STEMI PCI. We implemented a multicenter, prospective registry for all STEMI patients in Vermont treated at a single PCI center. Each patient was routinely pre-loaded with dual antiplatelet therapy and 75% received an unfractionated heparin bolus prior to PCI. The utilization of bivalirudin bolus and continued 2 h infusion after PCI was routine with GPI bailout optional. 128 consecutive STEMI patients underwent primary PCI from October 1, 2008 to September 30, 2009. 92% of primary PCI patients received bivalrudin during and after the procedure with a 9% rate of bail out GPI. There was one case of probable or definite acute stent thrombosis (0.7%), and this single case occurred despite use of bailout GPI. Despite the prolonged infusion of bivalirudin, major bleeding occurred in only 1.7% of STEMI patients. In conclusion, prolonging bivalirudin for 2 h after STEMI PCI may be a promising method to alleviate acute stent thrombosis risk without losing the bleeding complication benefit of the bivalirudin strategy.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
Multicenter Vermont registry of 128 STEMI patients showed that a 2-hour bivalirudin infusion after primary PCI reduced acute stent thrombosis to 0.7% (one patient despite bailout GPI), with major bleeding of only 1.7%.
Warum dies für die Hirudotherapie relevant ist
Diese prospektive multizentrische Registerstudie evaluierte eine Strategie der Verlängerung der Bivalirudin-Infusion um 2 Stunden nach PCI bei 128 konsekutiven STEMI-Patientinnen und -Patienten mit dem Ziel, das in früheren Studien beobachtete Risiko einer akuten Stentthrombose zu verringern und dabei den Blutungssicherheitsvorteil von Bivalirudin zu erhalten. Es trat nur ein Fall (0,7 %) akuter Stentthrombose auf, und die Rate schwerer Blutungen betrug 1,7 %. Der Abstract erwähnt weder Hirudin noch Blutegel oder irgendeine Verbindung zur Hirudotherapie; auf Grundlage dieses Abstracts besteht keine vertretbare Verbindung zu Blutegeln. Darüber hinaus handelte es sich um ein unkontrolliertes Beobachtungsregister ohne Randomisierung oder Vergleichsgruppe, was die Stärke der Schlussfolgerungen begrenzt.
Zitation
Two hour bivalirudin infusion after PCI for ST elevation myocardial infarction.
Anderson PR et al. · Journal of Thrombosis and Thrombolysis, 2011
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