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. 2013 Sep-Oct;27(5):1262-7.
doi: 10.1111/jvim.12130. Epub 2013 Jul 1.

Thromboelastographic evaluation of dogs with congenital portosystemic shunts

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Free article

Thromboelastographic evaluation of dogs with congenital portosystemic shunts

D Kelley et al. J Vet Intern Med. 2013 Sep-Oct.
Free article

Abstract

Background: On plasma-based assays, dogs with congenital portosystemic shunts (CPSS) have changes in serum concentrations of both pro- and anticoagulant proteins, but how these abnormalities affect whole blood coagulation assays (eg, thromboelastography) are unknown.

Objectives: To conduct kaolin-activated thromboelastography (TEG) analysis in dogs with CPSS and to compare TEG coagulation status with clinical presentation, routine serum biochemistry, and plasma-based coagulation tests.

Animals: Twenty-one client-owned dogs with CPSS confirmed by ultrasound examination or nuclear scintigraphy.

Methods: In a prospective study, signalment, clinical presentation, TEG analysis, CBC, serum biochemistry, and hemostatic tests (platelet count, prothrombin time [PT], activated partial thromboplastin time [aPTT], quantitative fibrinogen, antithrombin [AT] activity, protein C [PC] activity, d-dimers, and factor VIII activity) were analyzed in dogs with CPSS.

Results: Dogs with CPSS had significantly shorter K values and increased angle, maximum amplitude (MA), and G values compared with the reference population. On plasma-based coagulation testing, dogs with CPSS had significantly prolonged PT, lower platelet counts, lower AT and PC activities, and increased d-dimers and factor VIII activity. Evaluation of G value defined 9/21 dogs with CPSS as hypercoagulable. These dogs were more likely to have hepatic encephalopathy (HE) than CPSS dogs that had normal coagulation.

Conclusions and clinical importance: TEG analysis detected hemostatic abnormalities consistent with a hypercoagulable state in some dogs with CPSS. The presence of a hypercoagulable state was 40 times more likely in dogs with symptomatic HE.

Keywords: Coagulation; Encephalopathy; Hepatic disease.

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