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Updated: Feb 13, 2026

Rapid Point-of-Care Assay of Enoxaparin Anticoagulant Efficacy in Whole Blood
Published on: October 12, 2012
Establishment of prophylactic enoxaparin dosing recommendations to achieve targeted anti-factor Xa concentrations in
Emily N Israel1, Christopher A Thomas1, Christopher W Mastropietro2
11Department of Pharmacy,Riley Hospital for Children at Indiana University Health,Indianapolis,IN,USA.
Insights
Standard enoxaparin doses are insufficient for preventing thrombosis in pediatric patients with congenital heart disease (CHD). Higher enoxaparin doses are needed to achieve therapeutic anti-factor Xa levels in this population.
Area of Science:
- Pediatric Cardiology
- Pharmacology
- Thrombosis Prevention
Background:
- Congenital heart disease (CHD) patients often require central venous catheters.
- Catheter-related thrombosis is a significant complication in these patients.
- Enoxaparin is used for prophylaxis, but optimal dosing is unclear.
Purpose of the Study:
- To evaluate the effectiveness of current enoxaparin prophylactic dosing regimens.
- To determine if standard doses achieve target anti-factor Xa concentrations in pediatric CHD patients.
- To assess enoxaparin's role in preventing central venous catheter-related thrombosis.
Main Methods:
- Retrospective review of pediatric patients (<2 years) with CHD receiving enoxaparin.
- Analysis of anti-factor Xa concentrations against a prophylactic goal range (0.25-0.49 IU/ml).
- Evaluation of standard empiric enoxaparin doses (0.75 mg/kg/dose <2 months, 0.5 mg/kg/dose ⩾2 months).
Main Results:
- Only 31 out of 47 patients achieved target anti-factor Xa levels.
- A significant proportion (60%) had sub-therapeutic levels.
- Higher median doses were required: 0.89 mg/kg/dose for <2 months and 0.79 mg/kg/dose for ⩾2 months.
Conclusions:
- Current enoxaparin prophylactic dosing regimens are inadequate for pediatric CHD patients.
- Higher doses are necessary to reach target anti-factor Xa concentrations.
- Further research is needed to confirm if dose titration prevents thrombosis.
Background:
Enoxaparin may be used to prevent central venous catheter-related thrombosis in patients with CHD. We aimed to determine whether current enoxaparin dosing regimens effectively achieve anti-factor Xa concentrations within prophylactic goal ranges in this patient population.
Methods:
We implemented a formal protocol aimed at reducing central venous catheter-related thrombosis in children with CHD in January, 2016. Standard empiric prophylactic enoxaparin dosing regimens were used - for example, 0.75 mg/kg/dose every 12 hours for patients <2 months of age and 0.5 mg/kg/dose every 12 hours for patients ⩾2 months of age - with anti-factor Xa goal range of 0.25-0.49 IU/ml. Patients <2 years of age who received enoxaparin and had at least one valid steady-state anti-factor Xa measurement between 25 January, 2016 and 31 August, 2016 were retrospectively reviewed.
Results:
During the study period, 47 patients had 186 anti-factor Xa concentrations measured, of which 20 (11%) were above and 112 (60%) were below the prophylactic goal range. Anti-factor Xa concentrations within the goal range were ultimately achieved in 31 patients. Median dose required to achieve anti-factor Xa concentrations within the prophylactic range was 0.89 mg/kg/dose (25, 75%: 0.75, 1.11) for patients <2 months (n=23 patients) and 0.79 mg/kg/dose (25, 75%: 0.62, 1.11) for patients ⩾2 months (n=8 patients).
Conclusions:
Enoxaparin doses required to achieve prophylactic anti-factor Xa concentrations in young children with CHD were consistently higher than the currently recommended prophylactic dosing regimens. Further study is needed to determine whether dose titration to achieve prophylactic anti-factor Xa concentrations is effective in preventing central venous catheter-related thrombosis.
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