American Society of Hirudotherapy

Bivalirudin anticoagulation for cardiopulmonary bypass during cardiac surgery

Scoping review published in Perfusion (2023)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewDrug DevelopmentClinical LiteratureMeshulami N et al. · Perfusion, 2025

Abstract

INTRODUCTION: Heparin is the primary anticoagulant for cardiopulmonary bypass (CPB) support during cardiac surgery. While widely used, ∼2% of cardiac surgery patients develop heparin-induced thrombocytopenia (HIT) and 4-26% develop heparin resistance. Bivalirudin is an alternative anticoagulant mainly used for percutaneous coronary interventions. Given the challenges associated with heparin anticoagulation, we conducted a review to explore the use of bivalirudin for CPB surgery. METHODS: PubMed and Embase scoping review included 2 randomized controlled trials, a retrospective comparison study, 3 pilot studies, and 30 case reports. To provide a contemporary series, we searched for articles published from 2010 to 2023. Our review included studies from both adult and pediatric populations. RESULTS: While data is limited, bivalirudin seems to supply similar effectiveness and safety as heparin for CPB anticoagulation. Across the three comparative studies, the heparin cohorts had a 0-9% mortality rate and 0-27% rate of major bleeding/reoperation compared to a 0-3% mortality and 0-6% major bleeding/reoperation rate for the bivalirudin cohorts. Bivalirudin was successfully used as an anticoagulant in a wide range of CPB surgeries (e.g., heart transplants, ventricular assisted device placements, and valve repairs). Successful patient outcomes were reported with bivalirudin infusion of ∼2 mg/kg/hour, activated clotting time monitoring (target >400 s or 2.5× baseline), use of cardiotomy suctions, minimization of stagnant blood, and post-bypass modified ultrafiltration. CONCLUSION: Bivalirudin is a safe and effective anticoagulant for CPB, especially for patients with HIT or heparin resistance. Further comparative research is called for to optimize bivalirudin utilization for CPB during cardiac surgery.

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

Publication typeJournal ArticleReview
Indexed MeSH termsHirudinsHumansRecombinant ProteinsPeptide FragmentsCardiopulmonary BypassAnticoagulantsCardiac Surgical ProceduresHeparinMale

Summary

A scoping review of bivalirudin for cardiopulmonary bypass (2 RCTs, a retrospective comparison, 3 pilot studies, 30 case reports, 2010-2023) found that across three comparative studies bivalirudin cohorts had 0-3% mortality and 0-6% major bleeding versus 0-9% and 0-27% with heparin.

Why This Matters for Hirudotherapy

This scoping review explores the use of bivalirudin as an alternative anticoagulant for cardiopulmonary bypass surgery, motivated by approximately 2% incidence of heparin-induced thrombocytopenia and 4–26% rate of heparin resistance in cardiac surgery patients. Drawing on two randomized controlled trials, a retrospective comparison, three pilot studies, and 30 case reports, the authors conclude that bivalirudin appears to provide similar safety and effectiveness to heparin for CPB across diverse cardiac procedures. The abstract does not mention hirudin, leeches, or any leech-derived compound. This is a review article without original data, does not involve leeches or hirudotherapy, and the authors note that comparative data remains limited and call for further research. 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)

Meshulami N, Murthy R, Meyer M, Meyer AD, Kaushik S. Bivalirudin anticoagulation for cardiopulmonary bypass during cardiac surgery. Perfusion. 2025;40(1):7-19. doi:10.1177/02676591231221708. PMID: 38084653

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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