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Safety and efficacy of fixed versus variable-dose prothrombin complex concentrate for emergent reversal of vitamin K antagonists: A systematic review and meta-analysis - 12/02/24

Doi : 10.1016/j.ajem.2023.11.066 
Melanie Smith Condeni a, , Kyle A. Weant b , Ron R. Neyens a , Evert A. Eriksson c , Todd A. Miano d, 1
a Medical University of South Carolina, MUSC Health, Department of Pharmacy, 150 Ashley Avenue, Charleston, SC 29425, United States of America 
b University of South Carolina, College of Pharmacy, Department of Clinical Pharmacy and Outcome Sciences, 715 Sumter St, Columbia, SC 29208, United States of America 
c Medical University of South Carolina, MUSC Health, Department of Surgery, 96 Jonathan Lucas St #312, Charleston, SC 29425, United States of America 
d Perelman School of Medicine at the University of Pennsylvania, Department of Biostatistics, Epidemiology, and Informatics, 3400 Civic Center Blvd, Philadelphia, PA 19104, United States of America 

Corresponding author.

Abstract

Study objective

Four-factor prothrombin complex concentrate (4F-PCC) is standard of care for emergent vitamin K antagonist (VKA) reversal but optimal dosing is uncertain. This meta-analysis estimated the proportion of patients treated with fixed dose (FD) 4F-PCC who achieved adequate reversal and compared safety and efficacy of FD versus weight-based dose (WB) strategies.

Methods

This review was conducted according to PRISMA guidelines. Medline and Scopus were searched and included studies evaluating FD regimens and comparing FD and WB for emergent VKA reversal. Data was pooled using random effects. Subgroup analyses examined heterogeneity. Risk of bias was assessed with Newcastle-Ottawa Scale and RoB2 score.

Results

Twenty-three studies (n = 2055) were included with twelve (n = 1143) comparing FD versus WB. The proportion of patients achieving goal INR with FD varied depending on the INR target, being significantly higher for INR <2 (90.9%, 95% Confidence Interval (CI) 87.2, 94.06) compared to INR <1.6 (70.97%, 95%CI 65.33, 76.31). Compared to WB, FD was less likely to achieve a goal INR <1.6 (Risk Difference (RD) −13%, 95% CI −21, −4) but achieved similar reversal for a goal INR <2.0, (RD −1%, 95%CI −7, 4). There was no difference in hospital mortality (RD 4%, 95%CI −2, 9) or thrombosis (RD 0.0%, 95%CI −3, 3).

Conclusion

FD VKA reversal was associated with significantly lower attainment of goal INR compared to WB with lower INR targets. This did not translate to differences in hospital mortality, but these results should be interpreted cautiously in light of the observational nature of the included studies.

El texto completo de este artículo está disponible en PDF.

Highlights

Optimal dosing of four-factor prothrombin complex concentrate (4F-PCC) for vitamin K antagonist reversal is uncertain.
Emerging interest in fixed dose 4F-PCC is due to potential decreased risk of thrombosis and cost.
When compared to variable dose 4F-PCC, fixed dose may decrease the attainment of goal INR.
This decrease did not translate to differences in patient centered outcomes between dosing schema.

El texto completo de este artículo está disponible en PDF.

Keywords : Anti-coagulation reversal, Four-factor prothrombin complex concentrate, Vitamin k antagonists, Intracranial hemorrhage, International normalized ratio, Thrombosis

Abbreviations : 4F-PCC, FD, NOS, ROB2, TBW, VKA, WB


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