Bivalirudin in Extracorporeal Membrane Oxygenation

J Cardiovasc Pharmacol. 2024 Dec 1;84(6):553-561. doi: 10.1097/FJC.0000000000001633.

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.

Publication types

  • Review

MeSH terms

  • Animals
  • Anticoagulants / administration & dosage
  • Anticoagulants / adverse effects
  • Anticoagulants / therapeutic use
  • Antithrombins* / administration & dosage
  • Antithrombins* / adverse effects
  • Antithrombins* / therapeutic use
  • Blood Coagulation / drug effects
  • Extracorporeal Membrane Oxygenation* / adverse effects
  • Hemorrhage* / chemically induced
  • Hirudins* / administration & dosage
  • Hirudins* / adverse effects
  • Humans
  • Peptide Fragments* / adverse effects
  • Peptide Fragments* / therapeutic use
  • Recombinant Proteins* / administration & dosage
  • Recombinant Proteins* / adverse effects
  • Recombinant Proteins* / therapeutic use
  • Risk Assessment
  • Risk Factors
  • Thrombosis* / prevention & control
  • Treatment Outcome

Substances

  • Hirudins
  • bivalirudin
  • Peptide Fragments
  • Recombinant Proteins
  • Antithrombins
  • Anticoagulants