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Updated: Feb 26, 2026

In Vitro Thrombosis Test for Ventricular Assist Devices
Published on: March 21, 2025
Coagulation monitoring correlation with heparin dose in pediatric extracorporeal life support
Katie Moynihan1,2,3, Kerry Johnson1, Lahn Straney4
11 Pediatric Intensive Care Unit, Lady Cilento Children's Hospital (LCCH), Brisbane, Australia.
Insights
Monitoring heparin anticoagulation during extracorporeal life support (ECLS) is challenging. Anti-Factor Xa activity (anti-Xa) and thromboelastogram (TEG®6s) showed better correlation with heparin dose but had unexplained variations, suggesting further research is needed.
Area of Science:
- Pediatric Critical Care Medicine
- Hematology
- Cardiovascular Surgery
Background:
- Extracorporeal Life Support (ECLS) is associated with significant thrombotic and hemorrhagic risks.
- Optimal anticoagulation monitoring during ECLS remains controversial, impacting patient outcomes.
Purpose of the Study:
- To compare the effectiveness of various coagulation tests in monitoring heparin anticoagulation in pediatric ECLS.
- To evaluate the correlation between heparin dose and coagulation test results, including anti-Factor Xa activity (anti-Xa), activated partial thromboplastin time (aPTT), activated clotting time (ACT), and thromboelastogram (TEG®6s) parameters.
Main Methods:
- Retrospective study of pediatric patients (<18 years) undergoing ECLS over 12 months.
- Collected data on anti-Xa, aPTT, ACT, and TEG®6s parameters, correlating them with unfractionated heparin infusion rates.
- Analyzed mean test results in relation to ECLS runs and the presence of thrombotic complications.
Main Results:
- Sixty-six percent of ECLS runs experienced thrombotic complications, with 22% PICU mortality.
- Heparin dose explained only 9.9-13.3% of the variation in anti-Xa and TEG®6s results, and less than 1% for aPTT and ACT.
- Lower mean anti-Xa levels were observed in non-survivors and runs complicated by thrombosis.
Conclusions:
- Anti-Xa and TEG®6s demonstrated the best correlation with heparin dose but had substantial unexplained variability.
- Individual variations and other factors significantly influence coagulation test results, necessitating further investigation.
- Population pharmacokinetic/pharmacodynamic modeling and prospective trials are crucial for optimizing heparin therapy in ECLS.
Objectives:
Extracorporeal Life Support (ECLS) risks thrombotic and hemorrhagic complications. Optimal anti-coagulation monitoring is controversial. We compared coagulation tests evaluating the heparin effect in pediatric ECLS.
Methods:
A retrospective study of children (<18yrs) undergoing ECLS over 12 months in a tertiary pediatric intensive care unit (PICU). Variables included anti-Factor Xa activity (anti-Xa), activated partial thromboplastin time (aPTT), activated clotting time (ACT) and thromboelastogram (TEG®6s) parameters: ratio and delta reaction (R) times (the ratio and difference, respectively, between R times in kaolin assays with and without heparinase). Test results were correlated with unfractionated heparin infusion rate (IU/kg/hr) at the time of sampling. Mean test results of each ECLS run were evaluated according to the presence/absence of complications.
Results:
Thirty-two ECLS runs (31 patients) generated 695 data-points for correlation. PICU mortality was 22% and the thrombotic complication rate was 66%. The proportion of variation in coagulation test results explained by heparin dose was 13.3% for anti-Xa, 11.9% for ratio R time, and 9.9% for delta R time, compared with <1% for ACT and aPTT. Incorporating individual variation, age and antithrombin activity in a model with heparin dose explained less than 50% of the variation in test results. Correlation varied according to age, day of ECLS run and between individuals, with parallel dose-response lines noted between patients. Significantly lower mean anti-Xa was observed in PICU non-survivors and runs with thrombosis.
Conclusion:
Lower anti-Xa was observed in ECLS runs with complications. Although absolute results from anti-Xa and TEG6®s showed the best correlation with heparin dose, a large proportion of variation in results was unexplained by heparin, while dose response was similar between individuals. Population pharmacokinetic/pharmacodynamic modelling is required, as well as prospective trials to delineate the superior means of adjusting heparin therapy to prevent adverse clinical outcomes.
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