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Published on: October 12, 2012
Effect of Exogenous Antithrombin Administration on Anti-Xa Levels in Infants Treated With Enoxaparin
Insights
Exogenous antithrombin III (ATIII) administration significantly increased enoxaparin
Area of Science:
- Pediatric Pharmacology
- Thrombosis Management
- Pharmacokinetics
Background:
- Low molecular weight heparin (LMWH) like enoxaparin is used in infants.
- Therapeutic monitoring of enoxaparin involves anti-Xa levels.
- Some infants may not achieve therapeutic anti-Xa levels with enoxaparin alone.
Purpose of the Study:
- To evaluate the effect of exogenous antithrombin III (ATIII) on enoxaparin's anti-Xa levels in infants.
- To assess changes in ATIII levels and safety outcomes.
Main Methods:
- Retrospective chart review of infants receiving both ATIII and enoxaparin.
- Analysis of anti-Xa and ATIII levels before and after ATIII administration.
- Recording of enoxaparin doses and any bleeding events.
Main Results:
- Administration of exogenous ATIII led to a significant median increase in anti-Xa levels (0.2 units/mL, p < 0.001).
- Median ATIII dose was 50 units/kg, with a median enoxaparin dose of 1.71 mg/kg.
- Median increase in ATIII levels was 16.5% (p < 0.001).
Conclusions:
- Exogenous ATIII significantly boosts anti-Xa levels in infants treated with enoxaparin.
- Routine ATIII use in infants on enoxaparin is not currently recommended.
- ATIII supplementation may be considered for infants failing to reach therapeutic anti-Xa levels with enoxaparin alone.
Objectives:
Determine the effect of exogenous antithrombin III administration on low molecular weight heparin anti-Xa levels in the context of enoxaparin dosing in infants.
Methods:
A retrospective chart review of infants receiving concomitant antithrombin III and enoxaparin. The primary objective of this study was to determine the median change in anti-Xa level with antithrombin III supplementation. Secondary objectives were to analyze the median change in antithrombin III levels after administration of exogenous antithrombin III, the dosing of antithrombin III, and the dose of enoxaparin throughout therapy. For a safety analysis, any bleeding events were recorded.
Results:
The study included 17 patients who received a total of 33 doses of antithrombin III. The median change in anti-Xa levels in infants receiving exogenous antithrombin III was 0.2 units/mL (p < 0.001). The median dose of antithrombin III was 50 units/kg and was administered when patients were receiving a median enoxaparin dose of 1.71 mg/kg. The median increase in antithrombin III levels was 16.5% (p < 0.001).
Conclusions:
These results demonstrated that administration of exogenous antithrombin III to infants who were being treated with enoxaparin results in a significant increase in anti-Xa levels. At this time, there is insufficient evidence to recommend routine administration of antithrombin III to infants on enoxaparin. However, antithrombin III supplementation could be considered a potential option for patients who are unable to adequately achieve therapeutic anti-Xa levels with enoxaparin alone.
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