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.
Summary
Prospective multicenter Vermont registry of 128 consecutive STEMI patients in whom bivalirudin with a 2-hour post-PCI infusion was routine; acute stent thrombosis occurred in one patient (0.7%) and major bleeding in 1.7%, suggesting the infusion may limit stent-thrombosis risk.
Why This Matters for Hirudotherapy
This prospective multicenter registry evaluated a strategy of extending bivalirudin infusion for 2 hours post-PCI in 128 consecutive STEMI patients, aiming to mitigate acute stent thrombosis risk seen in prior trials while preserving bivalirudin's bleeding-safety advantage. Only one case (0.7%) of acute stent thrombosis occurred, and major bleeding was 1.7%. Additionally, this was an uncontrolled observational registry without randomization or a comparator group, limiting the strength of its conclusions. Bivalirudin (formerly Hirulog) is a synthetic peptide anticoagulant designed partly on the C-terminal sequence of hirudin, the anticoagulant of the medicinal leech (Maraganore et al., 1990); this paper studies the drug, not leech therapy.
Citation
Reference (Vancouver style)
Anderson PR, Gogo PB, Ahmed B, Straight F, Terrien EF, Watkins MW, et al. Two hour bivalirudin infusion after PCI for ST elevation myocardial infarction. J Thromb Thrombolysis. 2011;31(4):401-406. doi:10.1007/s11239-010-0528-7. PMID: 21107655
Bibliographic details (authors, volume, pages, DOI) are taken from the PubMed record.
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