Case series of low dose four-factor prothrombin complex concentrate for anticoagulant reversal
International Journal of Development Research
Case series of low dose four-factor prothrombin complex concentrate for anticoagulant reversal
Received 08th June, 2019; Received in revised form 20th July, 2019; Accepted 17th August, 2019; Published online 28th September, 2019
Copyright © 2019, Waad H. Al-Kathiri and Anas A. Khan. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Introduction: Recent international guidelines recommend the use of 4-factor prothrombin complex concentrate (PCC4) over fresh frozen plasma (FFP) for reversal of oral anticoagulant in life-threatening bleeds. Although, thromboembolic complications were reported in many studies in patients who received PCC4. Objective: Describe the effectiveness and safety of low weight base dose (25mg/kg) 4-factor prothrombin complex concentrate (PCC4) in controlling bleeds event caused by oral anticoagulant. Methods: Retrospective case series included nine patients who visit Emergency department with acute bleeding events controlled with low weight base dose 4-factor prothrombin complex concentrate. Chart review was conducted between January 2017 and December 2018. International Normalized Ratio (INR), thromboembolic events and hypersensitivity reaction were documented. Results: Baseline mean [±SD] INR ([±5.3] 6.4), Anticoagulant caused Intracerebral hemorrhage in two patients, and Gastrointestinal bleeding was the most complication caused by anticoagulant. PCC4 was given in dosing range 25 unit/kg based on estimated patient weight, mean [±SD] INR ([±0.95] 1.6) was 60 minutes post PCC4, PCC4 contributed significant reduction in INR (p=0.02). Six patients reached INR < 1.5, two patients INR <2, and only one patient with INR 4.3. No addition PCC4 doses were needed to control the bleeding event. None of patients experienced a thromboembolic events or hypersensitivity reaction 30 days post PCC4. Conclusion: Low weight base dose (25 unit/kg) PCC4 contributed to efficient reduction of INR in patients with life-threatening bleeding with low risk of thromboembolism event. We recommend a larger study to evaluate INR rebound and re-bleeding for post PCC4 along with thromboembolism event beyond the 30 days.