4.6 Article

Anti-Xa Activity After Enoxaparin Prophylaxis In Hospitalized Patients Weighing Less Than Fifty-Five Kilograms

Journal

THROMBOSIS RESEARCH
Volume 132, Issue 6, Pages 761-764

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.thromres.2013.10.005

Keywords

Body weight; Inpatients; Low molecular weight heparin; Prophylaxis; Venous thromboembolism; Weight loss

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Introduction: Low-molecular-weight heparins are commonly used for the prophylaxis of thromboembolic disease. In contrast to therapeutic doses, recommended prophylactic doses are fixed (i.e., 40mg/day enoxaparin). Dosing of patients with extreme body weights has not been well studied, especially dosing of low weight patients. Objectives: To establish the anti-Xa activity that results from 40 mg/day enoxaparin in inpatients with body weight <= 55 kg. Patients/Methods: Cross-sectional study including inpatients older than 18 years, with body weight <= 55 kg, and whose treating physician found indication for 40 mg/day enoxaparin. We excluded patients with renal failure and those using oral anticoagulants. Anti-Xa activity was measured 3 hours after the second dose of enoxaparin. Statistical analyses were conducted to determine the effect of body weight on anti-Xa levels. Results: Average age was 72.5 years (interquartile range, 30) and median body weight was 49.7 kg (interquartile range, 7). Twenty-five percent of patients weighed <= 45 kg, 37.5% weighed 46-50 kg, and 37.5% weighed 51-55 kg. The mean anti-Xa activity was 0.54 +/- 0.18 IU/ml, and 60% of the patients exhibited activity >= 0.5 IU/ml. Weight and anti-Xa activity inversely correlated (Spearman's rho = -0.428, p = 0.001). Patients weighing = 45 kg exhibited higher anti-Xa activity (0.61 +/- 0.18 IU/ml, p = 0.008) than heavier patients and an odds ratio of 8 for anti-Xa level >= 0.5 IU/ml (95% CI: 1.42-45.06). Conclusions: Anti-factor Xa activity rises significantly when body weight decreases. Patients of low weight, especially those weighing <45 kg, exhibited an anti-Xa activity higher than the desired range for thromboembolic prophylaxis. (C) 2013 Elsevier Ltd. All rights reserved.

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