Four-Factor Prothrombin Complex Concentrate for the Reversal of Direct Oral Anticoagulants. (January 2021)

• Record Type: Journal Article
• Authors: Zada, Ilanit; Wang, Shan; Akerman, Meredith; Hanna, Adel
• Is Part Of: Journal of intensive care medicine. Volume 36:Number 1(2021)
• Page Start: 58
• Page End: 62
• Publication Date: 2021-01
• Subjects: Direct Oral Anticoagulants (DOACs) -- 4-factor PCC -- intracranial hemorrhage -- hematoma; Critical care medicine -- Periodicals; Critical Care -- Periodicals; Soins intensifs -- Périodiques; Soins intensifs; Périodique électronique (Descripteur de forme); Ressource Internet (Descripteur de forme); 616.02805
• DOI: 10.1177/0885066619882909
• Languages: English
• ISSNs: 0885-0666

Abstract

Background: The prevalence of direct oral anticoagulants (DOACs) has increased with continued evidence of their efficacy and ease of use. However, the rise in their utilization also surfaced a concern regarding their reversal in patients actively bleeding and/or those requiring invasive procedures. Up until 2018, there were several reversal options available including 4-factor prothrombin complex concentrate (4-factor PCC), activated charcoal, desmopressin, and tranexamic acid. Then, in 2018, andexanet alpha, a recombinant factor Xa, was approved for the reversal of apixaban and rivaroxaban in patients with life-threatening or uncontrolled bleeding. Nonetheless, because 4-factor PCC is more easily attainable and cost-effective, it continues to be the more favorable option for many health-care professionals. Methods: This retrospective chart review was conducted at NYU Winthrop Hospital in patients who received 4-factor PCC for the reversal of DOACs from January 2018 to July 2018. Patient charts were reviewed and relevant data was collected (admitting diagnosis, dose of 4-factor PCC utilized, etc). Results: Fifty-three patients were evaluated with 85% experiencing a positive response and complete recovery following the administration of 4-factor PCC; 8 (15%) patients died after receiving 4-factor PCC, none as a result of its administration; 3 patients died secondary to other underlying comorbidities, 4 patients died due to an intracranial hemorrhage, and 1 died due to hematoma of the tongue. Conclusion: Based on the results thus far, the use of 4-factor PCC may be a good treatment option in patients requiring DOAC reversal.