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Bivalirudin use in an infant with persistent clotting on unfractionated heparin
Insights
Bivalirudin offers a predictable alternative to heparin for infants with clotting disorders. This case study highlights its use in a neonate with heparin-induced thrombocytopenia, noting potential challenges with renal impairment.
Area of Science:
- Cardiology
- Pharmacology
- Pediatric Critical Care
Background:
- Heparin-induced thrombocytopenia (HIT) presents challenges in pediatric anticoagulation due to variable anti-thrombin levels.
- Direct thrombin inhibitors like bivalirudin offer an alternative with a more predictable mechanism of action.
- Bivalirudin's use is expanding in pediatrics for its anti-thrombin-independent properties.
Observation:
- A 2-month-old female with recurrent systemic thrombi despite unfractionated heparin infusion was treated with bivalirudin.
- Initial bivalirudin dosing at 0.1 mg/kg/h was increased to 0.58 mg/kg/h to achieve therapeutic activated partial thromboplastin time (aPTT) values.
- Therapeutic aPTTs were achieved, but the patient developed worsening renal impairment, drug accumulation, and sepsis.
Findings:
- Bivalirudin achieved therapeutic aPTTs in a pediatric patient with HIT.
- Worsening renal impairment led to bivalirudin accumulation and necessitated discontinuation.
- The patient ultimately succumbed to overwhelming sepsis.
Implications:
- Bivalirudin can be considered for pediatric HIT when heparin is ineffective or contraindicated.
- Careful monitoring for renal function and potential drug accumulation is crucial in pediatric bivalirudin therapy.
- Further research is needed to establish optimal dosing and safety profiles for bivalirudin in neonates and infants.
Abstract:
Bivalirudin is a direct thrombin inhibitor approved for use in adult patients with heparin-induced thrombocytopenia (HIT) undergoing percutaneous coronary intervention. Recently, its use in the pediatric population has increased due to its anti-thrombin-independent mechanism of action. As heparin products produce great inter- and intraindividual variability in pediatric patients, often due to decreased anti-thrombin concentrations in the first year of life, some practitioners have turned to direct thrombin inhibitors, such as bivalirudin, for more predictable pharmacokinetics and effects on bound and circulating thrombin. We report our experience using bivalirudin in a 2-month-old female with recurrent systemic thrombi despite continuous unfractionated heparin infusion. Due to the patient's inability to maintain therapeutic activated partial thromboplastin time (aPTT) values during heparin infusion, bivalirudin was initiated at 0.1 mg/kg/h and increased due to subtherapeutic aPTTs to a maximum of 0.58 mg/kg/h. Therapeutic aPTTs were achieved at the increased dose; however, the patient's worsening renal impairment with resultant drug accumulation and overwhelming sepsis on day 5 of therapy led to discontinuation of the infusion and the initiation of comfort measures.
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