Brachycephalic obstructive airway syndrome has features similar to obstructive sleep apnea in humans. Both syndromes predispose patients to chronic airway obstruction and can lead to chronic intermittent hypoxia.
Humans with obstructive sleep apnea have increased mortality risk due to possible development of cardiovascular (eg, myocardial infarction, arrhythmias, pulmonary hypertension, systemic hypertension) and thromboembolic disorders,1,2 which are thought to be associated with hypercoagulability. In one study, it was suggested that clinically healthy bulldogs develop a hypercoagulable state similar to human patients with obstructive sleep apnea.3
Hypercoagulability is a blood coagulation abnormality that increases the risk for blood clots in the arteries or veins. Traditional coagulation tests (ie, prothrombin time, activated partial thromboplastin time, activated coagulation time) do not typically detect a hypercoagulable state.4
Thromboelastography, a viscoelastic method for coagulation evaluation, is commonly used in human and veterinary patients. Thromboelastography can provide data about the entire coagulation system and assist in evaluation for hypercoagulability, hypocoagulability, and fibrinolysis disorders.4,5 It produces a standardized tracing with components that represent different stages and quality of clot formation and fibrinolysis.
This pilot study evaluated thromboelastography parameters in 5 severely affected (grade 3)6 dogs with brachycephalic obstructive airway syndrome (3 pugs, 1 Pekingese, and 1 bulldog) and in a control group (Labrador retrievers).7 Profound hypercoagulability and delayed fibrinolysis were identified in all severely affected dogs as compared with controls.