Abstract

Our study objective was to identify a subcutaneous enoxaparin dosage that provided a consistent anticoagulant intensity in dogs. Our hypotheses were that a dose of 0.8mg/kg would provide inconsistent anticoagulation, a higher dose would provide consistent anticoagulation over a greater duration of time, and viscoelastometry would effectively monitor the anticoagulant status. Six healthy dogs received two subcutaneous enoxaparin doses (0.8 and 2mg/kg) for anti-Xa activity determinations and pharmacokinetic modeling. Based on calculations derived from these results, 1.3mg/kg, SC, q8h was administered for seven doses. Target ranges for anticoagulant intensity were defined as anti-Xa activity of 0.5-1U/ml, and change from baseline of two viscoelastometric parameters: activated clotting time (ΔACT; ≥40s), and clot rate (CRpost; ≤20U/min). Following an initial injection at 1.3mg/kg, anti-Xa activity of 5/6 dogs reached or exceeded the target range. Following the final dose, anti-Xa activity reached or exceeded the target range in all dogs, and ΔACT and CRpost values exceeded target for 2-6 and 4-12h, respectively. At an enoxaparin dosage of 1.3mg/kg, SC, q8h, anti-Xa activity was consistently above the minimum threshold of the target range; however, the safety of this dosage remains to be determined.

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