
Antithrombotic Effect of Enoxaparin in Clinically Healthy Cats: A Venous Stasis Model
Author(s) -
Van De Wiele C.M.,
Hogan D.F.,
Green H.W.,
Sederquist K.D.
Publication year - 2010
Publication title -
journal of veterinary internal medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.356
H-Index - 103
eISSN - 1939-1676
pISSN - 0891-6640
DOI - 10.1111/j.1939-1676.2009.0412.x
Subject(s) - medicine , cats , thrombus , antithrombotic , fibrinogen , thrombosis , low molecular weight heparin , anesthesia , surgery , cardiology
Background: Systemic arterial thromboembolic events are a serious complication of cardiac disease in cats. Objectives: To determine if enoxaparin induces an antithrombotic effect in cats at a dosage of 1 mg/kg SC q12h and if this antithrombotic effect is predicted by anti‐Xa activity. Animals: Fourteen clinically healthy cats were divided into 3 groups: control (4 cats), treated and assessed at 4 hours (5 cats), and treated and assessed at 12 hours (5 cats). Methods: A venous stasis model was used and the extent of thrombus formation estimated by measuring thrombus weight and accretion of 125 I‐fibrinogen. Plasma anti‐Xa activity was measured in treated cats. Results: There was a significant reduction in thrombus formation in the 4 h group compared with control (median weight, 0.000 versus 0.565 mg/mm, P < .01; median % 125 I‐fibrinogen accretion, 0.0 versus 42.0%, P < .01). There was a reduction in thrombus formation in the 12 h group (median weight, 0.006 mg/mm, P = .09; median % 125 I‐fibrinogen accretion, 3.83%, P = .09) but this reduction was not significant. The median percent thrombus inhibition for treated cats was 100.0% at 4 hours and 91.4% at 12 hours. Plasma anti‐Xa activity was not significantly correlated with thrombus formation. Conclusions and Clinical Importance: This pilot study demonstrates that enoxaparin, when administered at a dosage of 1 mg/kg SC q12h, produces an antithrombotic effect in a venous statsis model in clinically healthy cats. Furthermore, this study demonstrates that anti‐Xa activity is a poor predictor of enoxaparin's antithrombotic effect.