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Use of bivalirudin for anticoagulation in pediatric extracorporeal membrane oxygenation (ECMO)
Shubhi Kaushik1, Kim R Derespina1, Swati Chandhoke2
1Division of Pediatric Critical Care Medicine, Kravis Children's Hospital at Mount Sinai, New York, NY, USA.
Insights
Bivalirudin shows promise for anticoagulation in pediatric extracorporeal membrane oxygenation (ECMO) patients, potentially offering stable management. Further multicenter studies are needed to confirm these findings in pediatric anticoagulation.
Area of Science:
- Pediatric Critical Care Medicine
- Cardiovascular Surgery
- Pharmacology
Background:
- Extracorporeal membrane oxygenation (ECMO) requires effective anticoagulation in pediatric patients.
- Heparin is a common anticoagulant, but concerns like heparin-induced thrombocytopenia (HIT) exist.
- Bivalirudin offers an alternative anticoagulant with a different mechanism of action.
Purpose of the Study:
- To evaluate the efficacy and safety of bivalirudin compared to heparin for anticoagulation in pediatric ECMO patients.
- To analyze outcomes including activated partial thromboplastin time (aPTT) control, bleeding events, and mortality.
- To assess bivalirudin's role as both primary and secondary anticoagulant in this population.
Main Methods:
- Retrospective study of pediatric patients (<18 years) on ECMO from January 2016 to December 2019.
- Comparison of patients receiving bivalirudin versus heparin for anticoagulation.
- Data collection included demographics, ECMO details, anticoagulation parameters (aPTT), bleeding events, and mortality.
Main Results:
- Eight pediatric patients received bivalirudin primarily for anticoagulation.
- The bivalirudin group showed a higher proportion of aPTT values within the therapeutic range (65% vs. 44% in the first 7 days).
- Primary bivalirudin use was associated with lower dose requirements and comparable bleeding rates to the heparin group.
Conclusions:
- Bivalirudin may provide stable and effective anticoagulation in pediatric patients undergoing ECMO.
- Its use, particularly as a primary agent, warrants further investigation.
- Larger, multicenter studies are necessary to validate these preliminary findings and establish optimal protocols.
Abstract:
This study describes the use of bivalirudin in children on extracorporeal membrane oxygenation (ECMO). Pediatric patients receiving bivalirudin were compared to patients receiving heparin as the anticoagulant on ECMO. Data was collected for children under 18 years of age supported by ECMO from January 2016 to December 2019. Data collected included demographics, diagnosis, ECMO indication, type, and duration, indication for bivalirudin use, dose range, activated partial thromboplastin time (aPTT) levels, minor and major bleeding, hemolysis, and mortality. Forty pediatric patients received ECMO; eight received bivalirudin primarily for anticoagulation. The median age was 4 months (IQR 0.5, 92) in the heparin cohort, 0.6 months (IQR 0.0, 80.0) in the primary bivalirudin cohort. The indication for ECMO was respiratory in 5 patients (18%) in the heparin group versus 6 (75%) in the primary bivalirudin group, cardiac in 18 (67%) in heparin versus 1 (12.5%) in primary bivalirudin, and extracorporeal-cardiopulmonary resuscitation (E-CPR) in 4 (15%) in heparin versus 1 (12.5%) in primary bivalirudin. Bivalirudin was the initial anticoagulant for eight patients (66.6%) while three (25%) were switched due to concern for heparin-induced thrombocytopenia (HIT) and one (8%) for heparin resistance. The median time to achieve therapeutic aPTT was 14.5 hours compared to 12 hours in the heparin group. Sixty-five percent of aPTT values in the bivalirudin and 44% of values in the heparin group were in the therapeutic range in the first 7 days. Patients with primary bivalirudin use had significantly lower dose requirement at 12 (p = 0.003), 36 (p = 0.007), and 48 (p = 0.0002) hours compared to patients with secondary use of bivalirudin. One patient (12.5%) had major bleeding, and two patients (25%) required circuit change in the primary bivalirudin cohort. Bivalirudin may provide stable and successful anticoagulation in children. Further large, multicenter studies are needed to confirm these findings.
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