The Journal of Informed Pharmacotherapy 2004;15:405.
Sharon H. Ho, B.Sc.(Pharm), John K. Wu, MBBS, MSc, FRCPC, Donald P. Hamilton,
B.Sc.(Pharm), David B.
Dix, MBChB, FRCPC, and Louis D. Wadsworth, MB, ChB, FRCPath, FRCPC
Department of Pharmacy, Division of Hematology/Oncology/BMT, and Division of Hematopathology, British Columbia's Children's Hospital, Vancouver, BC, Canada; Faculty of Pharmaceutical Sciences, Department of Pediatrics, and Department of Pathology, University of British Columbia, Vancouver, BC, Canada.
Canadian Society of Hospital Pharmacists (British Columbia Branch) Residency Research Presentation Night, Vancouver, British Columbia, Canada. May 2003.
To evaluate the ability of published dosage guidelines for enoxaparin to achieve therapeutic anticoagulation and to determine whether the routine monitoring of anti-Xa levels is still necessary at a tertiary care pediatric institution.
A major Canadian tertiary pediatric acute care teaching hospital.
Consecutive charts were reviewed for all patients receiving treatment doses of enoxaparin over a 4 year period (1998-2002).
Sixty-six percent (25/38) of the anti-Xa levels were within the recommended therapeutic range (0.5 - 1.0 (+ 10%)
U/mL). The success rates of achieving therapeutic levels were 17%, 67%, 67%, 91%, and 67%, for patients < 2 months, >2 months - 1 year, >1-6 years, >6 - 12 years, and > 12 years of age, respectively.
Thirty-seven percent of patients reported adverse effects. The most common effects were injection site related bruising and minor bleeds. One patient experienced a non-life threatening major bleed.
The majority of patients achieved therapeutic anticoagulation when dosed according to the published guidelines. Pediatric patients with cardiac conditions, renal insufficiency or who are younger than 2 months were more likely to require dosage adjustments to achieve the therapeutic range. Routine monitoring of anti-Xa levels may be necessary in these patient populations. Enoxaparin appears to be well tolerated in our patient population.
Copyright © 2003 by the Journal of Informed Pharmacotherapy. All rights reserved.