Release Notes:
Appendix HTJC
Version 2016B1
Appendix H
Miscellaneous Tables
Table 2.1 VTE Prophylaxis Inclusion Table
Note: This table is not meant to be an inclusive list of all available prophylaxis; rather it represents current information available at the time of publication.
1 The U.S. Food and Drug Administration (FDA) has approved Eliquis (apixaban) to reduce the risk of stroke and systemic embolism in patients with non-valvular atrial fibrillation or to reduce the risk of blood clots, deep vein thrombosis (DVT) and pulmonary embolism (PE) following knee or hip replacement surgery only. It is additionally approved for treatment of DVT and PE and for the reduction in the risk of recurrent DVT and PE following initial therapy.
2 The U.S. Food and Drug Administration has approved Xarelto (rivaroxaban) to reduce the risk of blood clots, deep vein thrombosis (DVT) and pulmonary embolism (PE) following knee or hip replacement surgery only. It is additionally approved: to reduce the risk of stroke in patients with non-valvular atrial fibrillation; for treatment of DVT or PE; to reduce the risk of recurrent DVT and PE following initial treatment.
3 The FDA approved edoxaban (Savaysa) to reduce the risk of stroke and dangerous blood clots (systemic embolism) in patients with atrial fibrillation that is not caused by a heart valve problem. Savaysa has been approved to treat deep vein thrombosis (DVT) and pulmonary embolism (PE) in patients who have already been treated with anti-clotting drug administered by injection or infusion (parenterally), for five to ten days.
Table 2.6 Qualifiers and Modifiers Table
Note: These guideleines apply only to those data elements that refer to them in their Guidelines for Abstraction Exclusion list(s)
Table 2.7 Anticoagulation Therapy Table