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Thromboembolic outcomes after use of a four‐factor prothrombin complex concentrate for vitamin K antagonist reversal in a real‐world setting
Author(s) -
Joseph Ranjit,
Burner James,
Yates Sean,
Strickland Amanda,
Tharpe William,
Sarode Ravi
Publication year - 2016
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1111/trf.13406
Subject(s) - medicine , vitamin k antagonist , incidence (geometry) , prothrombin complex concentrate , thrombosis , risk factor , pediatrics , surgery , warfarin , atrial fibrillation , physics , optics
BACKGROUND A four‐factor prothrombin complex concentrate (4F‐PCC) was recently licensed in the United States for urgent vitamin K antagonist (VKA) reversal based on two randomized clinical trials. These studies excluded patients at high risk of thrombosis; therefore, the risk of thrombotic complications in unselected patients remains a concern. STUDY DESIGN AND METHODS This study retrospectively evaluated the incidence of thromboembolic events (TEEs) and death in patients who received 4F‐PCC for VKA reversal. The study included 113 consecutive patients who were 18 years of age and older and were administered 4F‐PCC for VKA reversal. The incidence of TEE and deaths was evaluated for up to 60 days after PCC administration or until the end of hospitalization, whichever came later. RESULTS Seven (6.2%) patients developed TEEs and 17 (15%) patients died. PCC administration was probably related to TEE and subsequent death in two (1.8%) patients. Multivariate analysis revealed that a diagnosis of Factor V Leiden or antiphospholipid syndrome was predictive of TEE, and active malignancy was predictive of death. CONCLUSION This study supports the safety of 4F‐PCC for urgent VKA reversal even in unselected patients. The underlying type of hypercoagulable state and the dose of PCC may influence the incidence of TEE.