American Society of Hirudotherapy

Off-pump coronary artery bypass with bivalirudin for patients with heparin-induced thrombocytopenia or antiplatelet factor four/heparin antibodies

Multicenter clinical trial published in Annals of Thoracic Surgery (2007)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Clinical trialClinical LiteratureDrug DevelopmentDyke CM et al. · Annals of Thoracic Surgery, 2007

Abstract

BACKGROUND: This study assessed the use of bivalirudin as an alternative anticoagulant in patients with heparin-induced thrombocytopenia-thrombotic syndrome (HIT/TS) or antiplatelet factor four-heparin (anti-PF4/H) antibodies undergoing off-pump coronary artery bypass (OPCAB). METHODS: In a prospective, open-label, multicenter study, fifty-one patients with documented anti-PF4/H antibodies and (or) HIT/TS underwent OPCAB with bivalirudin anticoagulation (0.75 mg/kg i.v. bolus, 1.75 mg/kg/hour infusion). Procedural success (absence of death, Q-wave myocardial infarction, repeat revascularization, and stroke), bleeding, and transfusion at day seven/discharge, thirty days, and twelve weeks were assessed. RESULTS: Thirty-five patients (67%) were included with positive anti-PF4/H antibodies and no thrombocytopenia or thrombosis, eleven patients (22%) had thrombocytopenia, and five patients had clinical HIT/TS (10%). Procedural success at seven days/discharge was achieved in forty-seven patients (92%), while procedural success at thirty days and twelve weeks was 88%. There were no deaths. Chest tube output over the first twenty-four hours was 936 +/- 525 mL and twenty-five patients received a red blood cell transfusion during their hospitalization. Two patients required reexploration for persistent postoperative hemorrhage. CONCLUSIONS: Bivalirudin was an effective alternative anticoagulant for patients with HIT/TS or circulating anti-PF4/H antibodies undergoing OPCAB, with high rates of procedural success and an acceptable incidence of bleeding or transfusions.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeClinical TrialJournal ArticleMulticenter Study
Indexed MeSH termsAgedAntibodiesAnticoagulantsCoronary Artery Bypass, Off-PumpFemaleHeparinHirudinsHumansMaleMiddle AgedPeptide FragmentsPlatelet Factor 4Prospective StudiesRecombinant ProteinsThrombocytopenia

Summary

In a prospective multicenter trial, 51 OPCAB patients with HIT/TS or anti-PF4/heparin antibodies received bivalirudin (0.75 mg/kg bolus, 1.75 mg/kg/hour infusion); procedural success was 92% at 7 days/discharge and 88% at 12 weeks, with no deaths and an acceptable rate of bleeding or transfusion.

Why This Matters for Hirudotherapy

This prospective, open-label, multicenter study evaluated bivalirudin as an alternative anticoagulant in 51 patients with heparin-induced thrombocytopenia or anti-PF4/heparin antibodies undergoing off-pump coronary artery bypass (OPCAB). Bivalirudin anticoagulation (0.75 mg/kg bolus, 1.75 mg/kg/hour infusion) achieved procedural success in 92% at day seven/discharge and 88% at twelve weeks, with no deaths. Bleeding outcomes included mean 24-hour chest tube output of 936 ± 525 mL, red blood cell transfusion in 25 patients, and reexploration for hemorrhage in 2 patients. The abstract contains no mention of leeches, hirudotherapy, or the leech secretome. 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)

Dyke CM, Aldea G, Koster A, Smedira N, Avery E, Aronson S, et al. Off-pump coronary artery bypass with bivalirudin for patients with heparin-induced thrombocytopenia or antiplatelet factor four/heparin antibodies. Ann Thorac Surg. 2007;84(3):836-839. doi:10.1016/j.athoracsur.2007.04.007. PMID: 17720385

Bibliographic details (authors, volume, pages, DOI) are taken from the PubMed record.

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