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Rapid Point-of-Care Assay of Enoxaparin Anticoagulant Efficacy in Whole Blood
Published on: October 12, 2012
Enoxaparin for neonatal thrombosis: a call for a higher dose for neonates
Janet I Malowany1, Paul Monagle, David C Knoppert
1Schulich School of Medicine & Dentistry, University of Western Ontario, London, Ontario, Canada N6A 5C1.
Insights
Current enoxaparin dosing for neonatal thrombosis may be insufficient. Recent studies suggest higher doses are needed for both term and preterm neonates to achieve therapeutic levels, with careful consideration of bleeding risks.
Area of Science:
- Neonatal Medicine
- Pediatric Hematology
- Pharmacology
Background:
- Enoxaparin is the standard anticoagulant for neonatal thrombosis.
- Current treatment guidelines are based on limited data from a small cohort of infants.
- Emerging evidence suggests higher enoxaparin doses may be required in neonates.
Purpose of the Study:
- To review and synthesize current data on enoxaparin use in neonates.
- To evaluate the efficacy and safety of different enoxaparin dosages.
- To inform updated treatment recommendations for neonatal thrombosis.
Main Methods:
- Systematic literature search of MEDLINE and conference proceedings (1996-2007).
- Inclusion of 8 papers, 4 abstracts, and 1 review article.
- Analysis of data from 240 neonates treated with enoxaparin.
Main Results:
- Mean enoxaparin maintenance doses ranged from 1.48 to 2.27 mg/kg every 12 hours.
- Higher doses (1.9-2.27 mg/kg q12h) were observed in preterm neonates.
- Enoxaparin achieved complete or partial resolution in 59-100% of cases, with minor side effects common and major bleeding in 0-19% of patients.
Conclusions:
- Increased enoxaparin experience indicates higher doses are necessary for therapeutic anti-factor Xa levels.
- Suggested starting doses: 1.7 mg/kg q12h for term and 2.0 mg/kg q12h for preterm neonates.
- Further prospective studies are needed to confirm optimal initial enoxaparin dosing in neonates.
Introduction:
Enoxaparin is the current anticoagulant of choice for neonatal thrombosis. Present neonatal treatment guidelines of 1.5 mg/kg every 12 hours (q12 h) are extrapolated primarily from an earlier study with 9 infants less than 2 months of age. More recent studies indicate an increased dose requirement for neonates.
Materials And Methods:
Relevant data from articles and abstracts were identified by searching MEDLINE and pediatric and hematology conference proceedings.
Results:
Publications between 1996 and 2007 included 8 papers, 4 abstracts and 1 review article with primary research documenting enoxaparin use in 240 neonates. The mean maintenance dose of enoxaparin ranged from 1.48 to 2.27 mg/kg q12 h for all infants, but was higher for preterm neonates at 1.9-2.27 mg/kg q12 h. The efficacy of enoxaparin, causing either complete or partial resolution was between 59 and 100%. Minor side effects were common and adverse events (major bleeding) occurred in 12 patients (0-19%).
Conclusions:
Increased experience with enoxaparin use in neonates in the past decade has indicated higher doses to achieve accepted target anti-factor Xa values. The long-term use of indwelling catheters (Insuflon catheter) for enoxaparin administration may need to be reevaluated in ELBW infants. Suggested starting doses of enoxaparin are 1.7 mg/kg q12 h for term neonates and 2.0 mg/kg q12 h for preterm neonates if there is no considerable bleeding risk. However, further prospective studies are needed to validate an increased initial dose of enoxaparin.
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