Evaluation of weight based enoxaparin dosing on anti-Xa concentrations in patients with obesity.
Anti-Xa
Anticoagulation
Enoxaparin
Low-molecular weight heparin
Morbid obesity
Obesity
Journal
Journal of thrombosis and thrombolysis
ISSN: 1573-742X
Titre abrégé: J Thromb Thrombolysis
Pays: Netherlands
ID NLM: 9502018
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
pubmed:
5
4
2019
medline:
20
2
2020
entrez:
5
4
2019
Statut:
ppublish
Résumé
Current treatment dose of enoxaparin is based on total body weight (TBW), however dosage in obesity remains unclear. "Dose capping" commonly occurs if TBW > 100 kg minimising bleeding risk. However, this may result in under-dosing and increasing embolisation risk. The primary objective evaluated efficacy of current dosing strategies in obese patients and determined if resultant anti-Xa concentrations (aXaC) were therapeutic. The secondary objective was to investigate if an uncapped 0.75-0.85 mg/kg (TBW) twice daily dose, advocated by previous authors, results in therapeutic aXaC (0.5-1.0 IU/ml). This retrospective study included 133 patients with a median TBW of 128 kg, producing 59% therapeutic, 15% sub-therapeutic and 26% supra-therapeutic aXaC. Approximately 60% of patients in each dose group (< 0.75, 0.75-0.85 and > 0.85 mg/kg) had a therapeutic aXaC, however the percentage of sub-therapeutic versus supra-therapeutic was higher in the < 0.75 (27% vs 9%) and > 0.85 mg/kg (10% vs 34%) groups respectively. Most patients who weighed 100-119 kg (TBW) received doses > 0.85 mg/kg, however 32% had toxic aXaC. Those between 120 and 139 kg (TBW) had a high percentage of therapeutic aXaC (87%) when dosed < 0.75 mg/kg and a high percentage of supra-therapeutic aXaC (71%) when dosed > 0.85 mg/kg; although numbers were low. Dose reduction occurred in patients > 140 kg (TBW), however < 0.75 mg/kg resulted in higher percentage of sub-therapeutic aXaC (42%). Dosing at 0.75-0.85 mg/kg results in 62% of therapeutic, 14% sub-therapeutic and 24% supra-therapeutic aXaC. This appears to be a "safe" starting dose-range, however all obese patients should have aXaC monitoring due to high inter-patient variability.
Identifiants
pubmed: 30945098
doi: 10.1007/s11239-019-01847-4
pii: 10.1007/s11239-019-01847-4
doi:
Substances chimiques
Enoxaparin
0
Factor Xa Inhibitors
0
Types de publication
Evaluation Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
387-393Références
Circulation. 1999 Oct 12;100(15):1593-601
pubmed: 10517729
Clin Pharmacol Ther. 2002 Sep;72(3):308-18
pubmed: 12235452
Br J Clin Pharmacol. 2003 Jul;56(1):96-103
pubmed: 12848781
Circulation. 2004 Jul 27;110(4):392-8
pubmed: 15249498
Clin Pharmacol Ther. 2007 Nov;82(5):505-8
pubmed: 17952107
Clin Pharmacokinet. 2010;49(2):71-87
pubmed: 20067334
P T. 2010 Feb;35(2):95-105
pubmed: 20221326
Br J Clin Pharmacol. 2010 May;69(5):520-8
pubmed: 20573088
Ther Drug Monit. 2010 Aug;32(4):482-8
pubmed: 20592650
J Thromb Thrombolysis. 2011 Aug;32(2):188-94
pubmed: 21465129
Br J Haematol. 2011 Oct;155(2):137-49
pubmed: 21848880
Thrombosis. 2011;2011:530183
pubmed: 22084664
J Thromb Thrombolysis. 2015 May;39(4):516-21
pubmed: 25087072
Clin Appl Thromb Hemost. 2015 Sep;21(6):513-20
pubmed: 25601898
Pharmacotherapy. 2015 Nov;35(11):1007-15
pubmed: 26598093
J Thromb Thrombolysis. 2016 Jan;41(1):15-31
pubmed: 26780737
Semin Thromb Hemost. 2019 Feb;45(1):94-99
pubmed: 30630208
N Engl J Med. 1997 Aug 14;337(7):447-52
pubmed: 9250846