ArticleThe journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG2026
Evaluation of Enoxaparin Dosing in Infants Greater Than 2 to 6 Months of Age, a Pre and Post Quasi Experiment.
Article in The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveEnoxaparin is regularly used to treat thromboembolism in children. Numerous retrospective studies suggest that infants and young children require higher enoxaparin doses to achieve therapeutic anti-factor Xa (AXA) concentration of 0.5 to 1.0 units/mL compared with adults.
methodsThis is a retrospective analysis of pre- and post-implementation of an increased initial dose of enoxaparin (1.2 mg/kg every 12 hours) for infants between 2 and 6 months of age. The objective is to compare the number of dose adjustments needed to achieve therapeutic AXA.
resultsA total of 64 patients were included 30 pre- and 34 post-guideline groups. In both the pre- and post-guideline dosing groups the number of dose adjustments required to achieve therapeutic AXA when adjusted per the ACCP guidelines was a median of 1 (p = 0.35). However, the first initial AXA was 0.3 units/mL in the pre-guideline group and 0.48 units/mL in the post-guideline group (p = 0.07). There were no documented instances of major bleeding events in either group.
conclusionThe results support the recommendation of an increased enoxaparin starting dose for therapeutic anticoagulation in the described patient population at the study site. A large prospective study is needed to determine specific dose recommendations that will achieve therapeutic AXA concentrations for the majority of infants and children of all ages.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.