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Published on: October 24, 2018
Anticoagulation monitoring during pediatric extracorporeal membrane oxygenation
Melania M Bembea1, Jamie M Schwartz, Nilay Shah
1Department of Anesthesiology and Critical Care, Johns Hopkins University, Baltimore, Maryland 21287, USA. mbembea1@jhmi.edu
Insights
Monitoring anticoagulation during extracorporeal membrane oxygenation (ECMO) is challenging. Activated clotting time (ACT) poorly correlates with antifactor Xa levels, necessitating cautious interpretation of results for pediatric ECMO patients.
Area of Science:
- Pediatric Intensive Care Medicine
- Hematology
- Cardiovascular Surgery
Background:
- Optimal anticoagulation monitoring during extracorporeal membrane oxygenation (ECMO) remains undetermined.
- Current monitoring methods may not accurately reflect anticoagulation status in pediatric patients.
Purpose of the Study:
- To prospectively evaluate coagulation monitoring assays in pediatric ECMO patients.
- To assess the correlation between activated clotting time (ACT), antifactor Xa, antithrombin (AT), and factor VIII activity (FVIII).
Main Methods:
- Prospective observational study in a tertiary pediatric intensive care unit.
- Collected blood samples from 34 children (35 ECMO runs) over 30 months.
- Measured ACT, antifactor Xa, AT, and FVIII at specified intervals during ECMO.
Main Results:
- Neonates had higher ACT and heparin doses but lower antifactor Xa compared to older children.
- Antifactor Xa, AT, and heparin infusion rates increased daily, while ACT decreased.
- ACT showed poor agreement with antifactor Xa (42%); AT influenced the ACT-heparin dose relationship.
Conclusions:
- Age and duration of ECMO significantly impact coagulation assay results.
- ACT is an unreliable measure for monitoring anticoagulation during pediatric ECMO.
- Further research is needed to establish optimal anticoagulation monitoring strategies for ECMO.
Abstract:
The best method of monitoring anticoagulation during extracorporeal membrane oxygenation (ECMO) is unknown. We conducted a prospective observational study in a tertiary pediatric intensive care unit. Antifactor Xa, antithrombin (AT), and factor VIII activity (FVIII) were measured in blood samples collected at 6, 12, and every 24 hours, respectively, of ECMO. We enrolled 34 children who underwent 35 ECMO runs from April 2008 to September 2010. Activated clotting time (ACT) and heparin doses were higher, whereas antifactor Xa levels were lower in neonates compared to infants/children. Median antifactor Xa was 0.4 IU/ml, median AT was 60%, and median FVIII was 67%. Heparin infusion rate, antifactor Xa, and antithrombin (AT) increased, FVIII was stable, and ACT decreased with each day on ECMO. ACT had poor agreement with antifactor Xa (42%). AT was inversely correlated with ACT (r = -0.33), even after adjusting for heparin dose, and positively correlated with antifactor Xa (r = 0.57). This study emphasizes the age differences as well as the variability over days of coagulation monitoring assays during ECMO. ACT is poorly correlated with antifactor Xa and AT modifies the relationship between ACT and the heparin dose, indicating that results should be interpreted with caution when managing anticoagulation on ECMO. Additional studies are warranted to determine optimal ECMO anticoagulation monitoring.
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