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. 2016 Jun 22;4:67. doi: 10.3389/fped.2016.00067

Table 2.

Comparison of UFH and bivalirudin.

Anticoagulant Mechanism of action Dosing range Reversible Monitoring tests Limitations
UFH Indirect – needs AT for maximal therapeutic effect 10–70 U/kg/h Protamine sulfate ACT, aPTT, anti-Xa, and TEG/ROTEM • Only one-third of UFH molecules has pentasaccharide sequence that binds AT, which leads to variable anticoagulation
• Does not inhibit clot-bound thrombin
• Thrombocytopenia
Bivalirudin Direct thrombin inhibitor 0.3–1.2 mg/kg/h No specific antidote, but bleeding may be mitigated with factor VIIa aPTT • Expect INR will increase
• Thrombosis with blood stasis (intracardiac and circuit)

UFH, unfractionated heparin; AT, antithrombin; TEG, thromboelastography; ROTEM, rotational thromboelastometry.