Aug 2026· Pediatric Critical Care Medicine· 1 citation· 21 references
Medicine
Abstract
Objectives
Bivalirudin, an IV direct thrombin inhibitor, is increasingly used as an alternative anticoagulant in pediatric patients on mechanical circulatory support, with heparin failure, or for heparin-induced thrombocytopenia. Data on its use for treatment or prevention of venous or arterial thromboses in children are limited. To describe the safety of bivalirudin in critically ill children for the treatment or prevention of venous and/or arterial thromboses.
Design
Retrospective review of patients under 18 years treated with bivalirudin between January 2019 and August 2024.
Setting
Quaternary care Children's Hospital.
PATIENTS
Descriptive analyses were conducted for all patients receiving bivalirudin. Primary outcomes include bleeding and thrombotic events. Secondary outcomes included time to therapeutic levels, dosing, and the association of therapeutic laboratory goals (via Partial Thromboplastin Time Hepzyme [PTTHz] and dilute thrombin time-derived bivalirudin levels) with adverse events.
Intervention
None.
Measurements
AND MAIN
Results
A total of 261 bivalirudin encounters in 229 patients were included in the analysis (median age, 0.51 yr; interquartile range, 0.13-3.92 yr). The most common indication was treatment of venous thrombosis (n = 133, 51%). Eighty-six bleeding events occurred in 261 encounters (33%) involving 61 of 229 patients (27%); 20 of 86 bleeding events were considered major (23.2%). Thrombotic progression or development of new thrombi occurred in 46 of 261 (17.6%) encounters (37/229; 16% patients) with 18 of 261 experiencing both bleeding and thrombotic events. Therapeutic PTTHz/bivalirudin levels were observed in 56.5% (26/46) of new thromboses/thrombotic progression and 57% (49/86) of bleeding events. Median starting dose and dose at first therapeutic level were 0.15 and 0.2 mg/kg/hr, respectively. Median time to achieve therapeutic anticoagulation was 0.56 days.
Conclusions
Bivalirudin, used in the setting of venous and/or arterial thromboses, rapidly achieves therapeutic levels. While use of bivalirudin is safe, clinically relevant bleeding and thrombotic rates on bivalirudin were frequent despite therapeutic ranges. These data highlight that bivalirudin use warrants close monitoring in critically ill children.
Objective: This study aimed to evaluate the use of bivalirudin as an alternative to conventional anticoagulant therapy with heparin in patients requiring venovenous extracorporeal membrane oxygenation (V-V ECMO) support for Acute Respiratory Distress Syndrome (ARDS), with a focus on dose titration, therapeutic range mo...
Özge Kuzgun, Kezban Özmen Süner, Fatih Toptan et al.· Turkish Journal of Intensive...· 0 citations
Bivalirudin has not been shown to have any significant difference to UFH on clinical outcomes in patients undergoing cardiac surgery, and as per current international guidelines, can be considered for safe use in those patients for whom UFH is contraindicated.
Matthew Cadd, S. Green, D. Puntis et al.· Annals of Cardiac Anaesthesi...· 0 citations
BACKGROUND
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Alessandra Bosch, F. Berger, Hitendu N. Dave et al.· Thrombosis Research· 0 citations
BACKGROUND
The administration of optimized venous thromboembolism (VTE) prophylaxis is critical in trauma patients. Guidance thus far has focused on initial enoxaparin dose selection and anti-factor Xa (anti-Xa) level monitoring. The need for monitoring and titrating prophylaxis in high-risk patients requiring prolonge...
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M. Sabri, Bahar Dehghan, Mohadeseh Ghasemi et al.· BMC Pediatrics· 0 citations
BACKGROUND
Nafamostat mesilate (NM), a synthetic serine protease inhibitor, has been used as an anticoagulant in patients undergoing extracorporeal circulatory support who have bleeding or heparin-related adverse effects. The safety and efficacy of NM-based anticoagulation in patients receiving Impella support who deve...
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