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Updated: May 26, 2026

Rapid Point-of-Care Assay of Enoxaparin Anticoagulant Efficacy in Whole Blood
Published on: October 12, 2012
Fluctuations of anti-Xa concentrations during maintenance enoxaparin therapy for neonatal thrombosis
Mirjana Lulic-Botica1, Madhvi Rajpurkar, Cindy Sabo
1Department of Pharmacy, Hutzel Women's Hospital, Detroit, MI, USA.
Insights
Anti-Xa concentrations frequently fluctuate in infants receiving enoxaparin for thrombosis, with therapeutic levels achieved sporadically. Despite this, enoxaparin demonstrates efficacy in resolving thrombosis in this population.
Area of Science:
- Neonatal Medicine
- Pediatric Thrombosis Management
- Pharmacokinetics in Infants
Background:
- Infants with thrombosis require anticoagulation, often with enoxaparin.
- Monitoring anti-Xa levels is crucial for enoxaparin therapy in neonates.
- Optimal dosing strategies for achieving therapeutic anti-Xa concentrations in infants are not well-established.
Purpose of the Study:
- To evaluate anti-Xa concentration fluctuations in infants treated with enoxaparin for thrombosis.
- To describe the clinical outcomes associated with enoxaparin therapy in this pediatric population.
Main Methods:
- Retrospective chart review of infants treated with enoxaparin in a Neonatal Intensive Care Unit.
- Abstraction of data including enoxaparin doses, anti-Xa concentrations, and clinical outcomes.
- Analysis of 143 anti-Xa concentrations from 26 infants.
Main Results:
- Therapeutic anti-Xa levels (0.5-1 U/mL) were achieved at a mean dose of 2.1 mg/kg, but only 27% of all measured concentrations were therapeutic.
- During maintenance therapy, 40% of anti-Xa concentrations were within the therapeutic range.
- Clot resolution was observed in 81% of infants, with minor bleeding in 4 and intracranial bleeding in 1; four infants died.
Conclusions:
- Anti-Xa concentrations exhibit significant fluctuations during maintenance enoxaparin therapy in infants.
- Enoxaparin appears effective for thrombosis resolution in infants, despite challenges in maintaining therapeutic anti-Xa levels.
- Further research is needed to optimize enoxaparin dosing and monitoring for improved outcomes in neonates.
Aim:
To evaluate fluctuations in anti-Xa concentrations in infants treated with enoxaparin for thrombosis and describe clinical outcomes.
Methods:
A retrospective chart review was performed on infants treated with enoxaparin in the Neonatal Intensive Care Unit, and data on enoxaparin doses, anti-Xa concentrations, clinical characteristics and outcomes were abstracted.
Results:
Our cohort (n = 26) had a median gestation of 36 (range, 23-41) weeks, birthweight of 2522 (510-3912) grams and 5-min Apgar score of 8(4-9). Fifteen (57.7%) infants were males. Thromboses was diagnosed at a median age of 22 (range, 1-97) days; enoxaparin was initiated at 27.5 (range, 4-98) days at a mean (SD) dose of 1.4 (0.3) mg/kg every 12 h. Therapeutic anti-Xa concentrations (0.5-1 U/mL) were achieved at a mean (SD) dose of 2.1 (0.6) mg/kg at 12.5 (12.2) days of treatment. Of the 143 anti-Xa concentrations, 39 (27%) were within the therapeutic range. During maintenance therapy following initial therapeutic anti-Xa concentration, 40% concentrations were therapeutic. Minor bleeding was noted in four infants and intracranial bleed in one infant; four infants died. During treatment, thrombocytopenia, renal and hepatic impairment during treatment were noted in 7, 2 and 4 infants, respectively. Clot resolution was observed in 21 (81%) infants.
Conclusions:
Anti-Xa concentrations fluctuate during maintenance enoxaparin therapy, with therapeutic levels being achieved only sporadically in young infants. Despite this, enoxaparin appears efficacious in thrombosis resolution. Further studies on the impact of stringent control of concentrations on outcomes in this population are warranted.
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