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Published on: May 26, 2015
Pediatric catheterization laboratory anticoagulation with bivalirudin
Thomas J Forbes1, Ziyad M Hijazi, Guy Young
1Division of Cardiology, Children's Hospital of Michigan, Detroit, Michigan, USA. tforbes@dmc.org
Insights
Bivalirudin is a safe and effective anticoagulant for pediatric percutaneous intravascular procedures. Its pharmacokinetic and pharmacodynamic response in children is predictable and similar to adults, supporting current dosing guidelines.
Area of Science:
- Pediatric Cardiology
- Pharmacology
- Interventional Cardiology
Background:
- Pediatric physicians face challenges with anticoagulation during procedures, particularly in neonates.
- Bivalirudin is a direct thrombin inhibitor used as an anticoagulant.
- Uncertainty exists regarding its optimal use in pediatric populations.
Purpose of the Study:
- To evaluate the safety, pharmacokinetics (PK), pharmacodynamics (PD), and dosing of bivalirudin in pediatric patients undergoing percutaneous intravascular procedures.
- To determine if adult dosing guidelines are applicable to pediatric populations.
- To assess the predictability of bivalirudin's anticoagulant effect in children.
Main Methods:
- A prospective study enrolled 110 pediatric patients (neonates to older children) undergoing percutaneous intravascular procedures for congenital heart disease.
- Patients received a weight-based dose of bivalirudin (0.75 mg/kg bolus, 1.75 mg/kg/hr infusion).
- Blood samples were collected for PK/PD analysis, and safety was monitored for bleeding and thrombosis events.
Main Results:
- Bivalirudin's PK/PD response in pediatric patients was predictable and similar to adults.
- Weight-normalized clearance was faster in neonates, decreasing with age.
- Bivalirudin concentrations were slightly lower in neonates but increased with age.
- Activating clotting time (ACT) response was consistent with adult studies, showing a reasonable correlation with bivalirudin levels.
- Major bleeding occurred in 1.8% and thrombotic events in 8.2% of patients.
Conclusions:
- Bivalirudin's pharmacokinetic and pharmacodynamic profile in pediatric patients is predictable and mirrors that of adults.
- Current adult dosing regimens for bivalirudin are safe and effective for pediatric intravascular procedures.
- The findings support the use of bivalirudin as a procedural anticoagulant in pediatric cardiology.
Background:
Pediatric physicians regularly face the problem of uncertain procedural anticoagulation in children, especially in neonates. We sought to evaluate the safety, plasma concentration (pharmacokinetics, PK), pharmacodynamics (PD), and dosing guidelines of bivalirudin when used as a procedural anticoagulant in pediatric percutaneous intravascular procedures.
Methods And Results:
Pediatric subjects undergoing percutaneous intravascular procedures for congenital heart disease were enrolled and received the current weight-based dose used in percutaneous coronary interventions (0.75 mg/kg bolus, 1.75 mg/kg/hr infusion). Blood samples for PK/PD analyses were drawn, and safety was evaluated by monitoring bleeding and thrombosis events. A total of 110 patients (11 neonates, 33 infants, 32 young children, and 34 older children) were enrolled; 106 patients received the protocol dose. The PK/PD response of bivalirudin was predictable and behaved in a manner similar to that in adults. Weight-normalized bivalirudin clearance rates were more rapid in neonates and decreased with increasing age. Bivalirudin concentrations were slightly lower in neonates, with a trend to an increase with age. Activating clotting time response was consistent with adult studies and prolonged in all age groups, and there was reasonable correlation between activating clotting time and bivalirudin plasma concentrations across all age groups. There were few major bleeding (2 of 110, 1.8%) or thrombotic events (9 of 110, 8.2%) reported.
Conclusions:
PK/PD response of bivalirudin in the pediatric population is predictable and behaves in a manner similar to that in adults. Using adult dosing, bivalirudin safely provided the expected anticoagulant effect in the pediatric population undergoing intravascular procedures for congenital heart disease.
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