Why the study?
The optimal antithrombin activity for low-molecular-weight heparin efficacy and the benefits of antithrombin III supplementation in premature infants with venous thromboembolism are unknown, with no neonatal-specific guidelines on target levels.
Does antithrombin III supplementation improve the achievement of therapeutic anti-Xa levels during enoxaparin treatment in a premature infant with venous thromboembolism?
Does antithrombin III supplementation improve the achievement of therapeutic anti-Xa levels during enoxaparin treatment in a premature infant with venous thromboembolism?
In a premature infant with an occlusive inferior vena cava thrombus, antithrombin III supplementation to achieve >40% activity was necessary to reach therapeutic anti-Xa levels with enoxaparin.
May inform ATIII use in select neonatal VTE cases; leaves open optimal targets and need for prospective trials.
The optimal antithrombin (AT) activity for low-molecular-weight heparin efficacy and the benefits of antithrombin III (ATIII) supplementation in premature infants diagnosed with venous thromboembolism are unknown. Currently, there are no neonatal-specific guidelines directing the appropriate target AT activity during supplementation. This case report describes a critically ill premature infant with a progressive, occlusive inferior vena cava thrombus who received supplemental ATIII during enoxaparin treatment. The patient did not achieve therapeutic anti-Xa levels despite increasing enoxaparin dosing to 3 mg/kg every 12 hours. ATIII supplementation sufficient to attain an AT activity of >40%, in combination with an enoxaparin dosing of >2 mg/kg every 12 hours, was needed to achieve therapeutic anti-Xa levels. Future large studies are needed to determine if there is an optimal target AT activity for critically ill premature infants.
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Shukla et al. (2021) studied this question.
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