Bivalirudin use in an infant with persistent clotting on unfractionated heparin
Case report published in Journal of Pediatric Pharmacology and Therapeutics (2011)
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.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
Two-month-old female with recurrent systemic thrombi unresponsive to unfractionated heparin; bivalirudin was titrated from 0.1 to 0.58 mg/kg/h and achieved therapeutic aPTTs before being discontinued due to renal impairment and sepsis.
Warum dies für die Hirudotherapie relevant ist
This case report describes bivalirudin use in a 2-month-old female with recurrent systemic thrombi despite continuous unfractionated heparin infusion. It reports that therapeutic aPTTs were achieved after dose escalation, but worsening renal impairment with drug accumulation and overwhelming sepsis led to discontinuation and initiation of comfort measures on day 5. The abstract does not mention leeches, hirudin, leech saliva, or hirudotherapy, so it provides no defensible connection to ASH's domain or the leech secretome. Its limitations are those of a case report: a single critically ill infant, no leech therapy, and no inference about hirudotherapy outcomes.
Zitation
Bivalirudin use in an infant with persistent clotting on unfractionated heparin.
Malloy KM et al. · Journal of Pediatric Pharmacology and Therapeutics, 2011
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