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Published on: December 31, 2015
Antithrombin III Supplementation in a Premature Infant: Is There a Target Antithrombin Level?
Insights
Optimal antithrombin (AT) activity for heparin efficacy in premature infants with venous thromboembolism remains unclear. This case suggests ATIII supplementation to >40% AT activity, with enoxaparin >2 mg/kg q12h, may be needed for therapeutic anti-Xa levels.
Area of Science:
- Neonatal medicine
- Pharmacology
- Hematology
Background:
- Optimal antithrombin (AT) activity for low-molecular-weight heparin (LMWH) efficacy in neonates is not established.
- There is a lack of neonatal-specific guidelines for antithrombin III (ATIII) supplementation targets.
- Venous thromboembolism (VTE) is a serious concern in premature infants.
Purpose of the Study:
- To describe a case of VTE in a premature infant treated with enoxaparin and ATIII supplementation.
- To investigate the required ATIII levels and enoxaparin dosing to achieve therapeutic anti-Xa levels in this patient.
- To highlight the need for further research into optimal AT activity targets in critically ill premature infants.
Main Methods:
- Case report of a critically ill premature infant with inferior vena cava thrombus.
- Treatment involved enoxaparin and supplemental ATIII.
- Monitoring of anti-Xa levels to assess therapeutic efficacy.
Main Results:
- The patient did not achieve therapeutic anti-Xa levels despite escalating enoxaparin doses up to 3 mg/kg every 12 hours.
- ATIII supplementation to achieve >40% AT activity, combined with enoxaparin >2 mg/kg every 12 hours, was necessary for therapeutic anti-Xa levels.
Conclusions:
- Achieving therapeutic anti-Xa levels in premature infants with VTE may require higher enoxaparin doses and ATIII supplementation.
- A target AT activity of >40% may be necessary in conjunction with specific enoxaparin dosing.
- Further large-scale studies are essential to determine optimal AT activity targets for critically ill premature infants receiving LMWH therapy.
Abstract:
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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