American Society of Hirudotherapy

Bivalirudin in Extracorporeal Membrane Oxygenation

Review published in Journal of cardiovascular pharmacology (2024)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewDrug DevelopmentDunham S et al. · Journal of cardiovascular pharmacology, 2024

Abstract

Extracorporeal membrane oxygenation (ECMO) is a mechanical support treatment modality used in patients with refractory cardiac and/or pulmonary failure. Bleeding and thrombotic complications associated with ECMO are inherent concerns that require careful management. Anticoagulation optimization may help mitigate these risks by providing more adequate therapeutic anticoagulation and lessen the bleed risk. Heparin, the most used anticoagulant, carries concerns for heparin-induced thrombocytopenia and possible resistance given its dependence on cofactors and circulating proteins to exert its pharmacologic effect. In contrast, bivalirudin, a direct thrombin inhibitor, exerts its effect independent of cofactors or plasma proteins, and possesses thrombin-binding and metabolism features that may confer advantages in ECMO management. This review of the evidence for bivalirudin utilization in ECMO suggests favorable outcomes in circuit-related thrombosis, bleeding, and dosing reliability. In addition, blood product utilization, circuit interventions, and success in ECMO decannulation and survival were positive findings associated with bivalirudin that merit consideration. Common questions and concerns relative to bivalirudin utilization, including laboratory monitoring, utilization in low-flow states, dosing considerations in renal replacement therapy, reversibility, and cost are also discussed in this review. Moreover, this review suggests that bivalirudin utilization presents the opportunity for ECMO management simplification.

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

Publication typeJournal ArticleReview
Indexed MeSH termsHirudinsExtracorporeal Membrane OxygenationHumansPeptide FragmentsRecombinant ProteinsAntithrombinsTreatment OutcomeHemorrhageThrombosisRisk FactorsBlood CoagulationAnticoagulantsAnimalsRisk Assessment

Summary

This review evaluates bivalirudin, a cofactor-independent direct thrombin inhibitor, as an ECMO anticoagulant, reporting benefits for thrombosis, hemorrhage, and dosing consistency, plus positive results for blood product use, circuit interventions, and decannulation, while discussing monitoring, low-flow dosing, renal replacement therapy, reversal, and cost.

Why This Matters for Hirudotherapy

This review examines the evidence for using bivalirudin—a direct thrombin inhibitor that acts independently of cofactors or plasma proteins—as an alternative to heparin for anticoagulation during extracorporeal membrane oxygenation (ECMO), discussing circuit thrombosis, bleeding, dosing, monitoring, renal replacement considerations, and cost. The authors suggest favorable outcomes and potential simplification of ECMO anticoagulation management. This is a review with no original data. 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)

Dunham S, Wieruszewski PM, Gerrald JE. Bivalirudin in Extracorporeal Membrane Oxygenation. J Cardiovasc Pharmacol. 2024;84(6):553-561. doi:10.1097/FJC.0000000000001633. PMID: 39259286

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

This website provides educational information and does not constitute medical advice, diagnosis, or treatment recommendations. Medicinal leech therapy carries clinically meaningful risks and should be performed only by qualified clinicians under institutionally approved protocols. FDA 510(k) clearance for medicinal leeches is limited to specific indications; investigational and off-label discussions are labeled accordingly. For patient-specific guidance, consult a qualified healthcare provider.