None

None

- pregnancy; - hemoglobin <80 g/l in the last 72 hours; - platelet count <50 x 109/l in the last 72 hours; - known fibrinogen <1.5 g/l (if testing deemed clinically indicated by the treating physician prior to the initiation of anticoagulation); - known inr >1.8 (if testing deemed clinically indicated by the treating physician prior to the initiation of anticoagulation); - patient already on intermediate dosing of lmwh that cannot be changed (determination of what constitutes an intermediate dose is to be at the discretion of the treating clinician taking the local institutional thromboprophylaxis protocol for high risk patients into consideration); - patient already on therapeutic anticoagulation at the time of screening (low or high dose nomogram ufh, lmwh, warfarin, direct oral anticoagulant (any dose of dabigatran, apixaban, rivaroxaban, edoxaban); - patient on dual antiplatelet therapy, when one of the agents cannot be stopped safely; - known bleeding within the last 30 days requiring emergency room presentation or hospitalization; - known history of a bleeding disorder of an inherited or active acquired bleeding disorder; - known history of heparin-induced thrombocytopenia; - known allergy to ufh or lmwh; - admitted to the intensive care unit at the time of screening; - treated with non-invasive positive pressure ventilation or invasive mechanical ventilation at the time of screening.

- pregnancy; - hemoglobin <80 g/l in the last 72 hours; - platelet count <50 x 109/l in the last 72 hours; - known fibrinogen <1.5 g/l (if testing deemed clinically indicated by the treating physician prior to the initiation of anticoagulation); - known inr >1.8 (if testing deemed clinically indicated by the treating physician prior to the initiation of anticoagulation); - patient already on intermediate dosing of lmwh that cannot be changed (determination of what constitutes an intermediate dose is to be at the discretion of the treating clinician taking the local institutional thromboprophylaxis protocol for high risk patients into consideration); - patient already on therapeutic anticoagulation at the time of screening (low or high dose nomogram ufh, lmwh, warfarin, direct oral anticoagulant (any dose of dabigatran, apixaban, rivaroxaban, edoxaban); - patient on dual antiplatelet therapy, when one of the agents cannot be stopped safely; - known bleeding within the last 30 days requiring emergency room presentation or hospitalization; - known history of a bleeding disorder of an inherited or active acquired bleeding disorder; - known history of heparin-induced thrombocytopenia; - known allergy to ufh or lmwh; - admitted to the intensive care unit at the time of screening; - treated with non-invasive positive pressure ventilation or invasive mechanical ventilation at the time of screening.