Assessing Anticoagulation in Neonates With Congenital Diaphragmatic Hernia During Extracorporeal Membrane Oxygenation: Does Anti-Factor Xa or Thromboelastometry Provide Additional Benefit?

2021 
Objective: The optimal management of anticoagulation in neonatal/pediatric patients during extracorporeal membrane oxygenation (ECMO) has not been established yet and varies greatly among ECMO centers worldwide. Therefore, we aimed to assess whether the use of anti-factor Xa assay and/or thromboelastometry correlate better than activated clotting time with heparin dose in newborns with congenital diaphragmatic hernia during ECMO and whether these coagulation assays correlate with thrombotic and/or hemorrhagic complications, when the management of anticoagulation is only based on activated clotting time values. Methods: A prospective observational study in a neonatal ECMO center was conducted. All neonates with congenital diaphragmatic hernia born in our institution between March 2018 and January 2019 and requiring support with venoarterial extracorporeal membrane oxygenation were included. A total of 26 extracorporeal membrane oxygenation runs were analyzed. During the study heparin dose was still adjusted according to activated clotting time values. Measurements of anti-factor Xa assay, activated partial thromboplastin time and a thromboelastometry from the same blood specimen were performed twice a day. Results: Anti-factor Xa levels showed a moderate correlation with heparin dose, whereas the other tests showed a weak correlation. Four patients (17.4%) had thrombotic complications, two patients (8.7%) experienced life-threatening bleedings and in eleven patients (47.8%) disseminated intravascular coagulation (DIC) occurred. Anti-factor Xa levels were lower in the group with thrombotic complications (0.23 IU/mL vs 0.27 IU/mL; p = 0.002), while activated partial thromboplastin time was higher in the group with hemorrhagic complications (69.4 s vs 59.8 s; p=0.01). In patients experiencing a DIC, heparin dose and anti-factor Xa levels were lower, whileno differences in activated clotting time and clotting time in INTEM and INTEM-HEPTEM were shown. Conclusions: Anti-factor Xa levels correlate better to heparin dose than activated clotting time. The use of anti-factor Xa assay instead of activated clotting time for dosing of unfractionated heparin could reduce thrombotic complications in neonates with congenital diaphragmatic hernia on ECMO. The thromboelastometry showed no additional benefit for this purpose.
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