American Society of Hirudotherapy

Role of bivalirudin for anticoagulation in adult perioperative cardiothoracic practice

Cardiothoracic anesthesia review published in Journal of Cardiothoracic and Vascular Anesthesia (2019)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewDrug DevelopmentErdoes G et al. · Journal of cardiothoracic and vascular anesthesia, 2020

Abstract

Bivalirudin, a direct thrombin inhibitor with a fast onset of action and short half-life, is often referred to as an alternative anticoagulant to a heparin/protamine regimen. Bivalirudin demonstrated promising results as an anticoagulant in cardiac surgery with and without cardiopulmonary bypass, postcardiotomy extracorporeal membrane oxygenation, interventional cardiology and endovascular procedures, and particularly in the treatment of patients with heparin-induced thrombocytopenia undergoing high-risk cardiac surgery. Currently, bivalirudin in cardiac surgery with cardiopulmonary bypass has a limited clinical spectrum, likely because the still obvious advantages of its competitor, heparin, outweigh it in terms of medical costs, established point-of-care monitoring systems, and availability of protamine as a reversal agent. The unique pharmacology of the drug also requires adjustment of surgical and perfusion strategy. In contrast, in off-pump coronary artery surgery, established protocols from interventional cardiology can be easily translated into the operating room. In this setting bivalirudin has the potential for a more important role in the future. Through a triple mechanism of action-inhibition of plasma thrombin, clot bound thrombin, and collagen-induced platelet activation-bivalirudin may perform better than heparin by attenuating the immediate postoperative prothrombotic state and thus positively impacting the early coronary graft patency after off-pump coronary artery bypass grafting. Further studies are necessary to better evaluate this niche field and discover further applications for this unique anticoagulant.

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

Publication typeJournal ArticleReview
Indexed MeSH termsAdultAnticoagulantsHeparinHirudin TherapyHirudinsHumansPeptide FragmentsRecombinant Proteins

Summary

Bivalirudin, a direct thrombin inhibitor, serves as an alternative to heparin/protamine in cardiac surgery, off-pump coronary surgery, ECMO, and heparin-induced thrombocytopenia, though its use in on-pump surgery remains limited by heparin's established cost and monitoring advantages.

Why This Matters for Hirudotherapy

This review examines bivalirudin, a direct thrombin inhibitor with a fast onset of action and short half-life, as an alternative anticoagulant to heparin/protamine in adult perioperative cardiothoracic practice, including cardiac surgery with and without cardiopulmonary bypass, postcardiotomy ECMO, interventional cardiology, and heparin-induced thrombocytopenia. The abstract discusses bivalirudin's triple mechanism of action—inhibition of plasma thrombin, clot-bound thrombin, and collagen-induced platelet activation—and its potential advantages in off-pump coronary artery surgery. The article reports no new primary data and focuses on a pharmaceutical agent's surgical applications. 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)

Erdoes G, Ortmann E, Martinez Lopez De Arroyabe B, Reid C, Koster A. Role of bivalirudin for anticoagulation in adult perioperative cardiothoracic practice. J Cardiothorac Vasc Anesth. 2020;34(8):2207-2214. doi:10.1053/j.jvca.2019.08.022. PMID: 31521492

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

Added to ASH library: May 27, 2026 · Site last updated: June 18, 2026

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