scholarly journals 413: COMPARISON OF PROTHROMBIN COMPLEX CONCENTRATE DOSING STRATEGIES IN CARDIOTHORACIC SURGERY PATIENTS

2021 ◽  
Vol 50 (1) ◽  
pp. 195-195
Author(s):  
Nicholas Barker ◽  
Meera Patel ◽  
William Bender ◽  
Sarah Burke
2020 ◽  
Vol 48 (1) ◽  
pp. 457-457
Author(s):  
Breyanna Reachi ◽  
Abby Hickman ◽  
Marie Rapier ◽  
Jenna Negrelli

2018 ◽  
Vol 46 (1) ◽  
pp. 608-608
Author(s):  
Sue Lee ◽  
Noelle de Leon ◽  
Ashley Thompson ◽  
Christine Baumgartner ◽  
Margaret Fang ◽  
...  

2015 ◽  
Vol 135 (1) ◽  
pp. 9-19 ◽  
Author(s):  
Nakisa Khorsand ◽  
Hilde A.M. Kooistra ◽  
Reinier M. van Hest ◽  
Nic J.G.M. Veeger ◽  
Karina Meijer

2020 ◽  
Vol 4 (17) ◽  
pp. 4208-4216
Author(s):  
Ravi Sarode ◽  
Katsuyuki Fukutake ◽  
Masahiro Yasaka ◽  
Michael A. Tortorici ◽  
Antoinette Mangione ◽  
...  

Abstract The indicated dose of 4-factor prothrombin complex concentrate (4F-PCC) for urgent vitamin K antagonist (VKA) reversal in patients with an international normalized ratio (INR) of 2 to 4 is 25 IU/kg, but there is no indicated dose for INR <2. We explored 4F-PCC dosing strategies for baseline INR <2. Clinical trial data were used to develop pharmacometric models for Factor X (FX) and FII, accounting for covariates including baseline INR. FX and FII levels over time were simulated for mean baseline INR levels of the clinical trial participants plus baseline INRs 3.1, 1.9, and 1.6. For each INR, 200 virtual male patients were simulated to evaluate 4F-PCC doses of 35, 25, 20, 15, 12.5, and 10 IU/kg. Given an elevated bleeding risk with VKA therapy in Japanese vs Western populations, results were stratified by Japanese and non-Japanese patients. Target levels of FX and FII were ≥50% activity at 30 minutes after dosing in ≥80% of patients. FX- and FII-time models were developed with 1088 FX observations from 193 patients and 1074 FII observations from 192 patients. Model-based simulations indicated that at baseline INR 3.1, ≥80% of patients achieved ≥50% FX and FII activity with 25 IU/kg and 20 IU/kg 4F-PCC, respectively; at baseline INR 1.9, corresponding doses were 20 IU/kg and 15 IU/kg 4F-PCC, and at baseline INR 1.6, corresponding doses were 15 IU/kg, and 10 IU/kg 4F-PCC. Trends in Japanese and non-Japanese patients were similar. In conclusion, low 4F-PCC doses (15-20 IU/kg) may be sufficient to achieve hemostatic levels of FX and FII in Japanese and non-Japanese patients with baseline INR <2.


1977 ◽  
Vol 137 (9) ◽  
pp. 1211-1213 ◽  
Author(s):  
R. T. DeWitt

2020 ◽  
Vol 32 (4) ◽  
pp. 605
Author(s):  
Erle H. Austin ◽  
Todd K. Rosengart ◽  
Harvey I. Pass ◽  
Ravi Ghanta ◽  
Richard D. Weisel

1988 ◽  
Vol 60 (02) ◽  
pp. 226-229 ◽  
Author(s):  
Jerome M Teitel ◽  
Hong-Yu Ni ◽  
John J Freedman ◽  
M Bernadette Garvey

SummarySome classical hemophiliacs have a paradoxical hemostatic response to prothrombin complex concentrate (PCC). We hypothesized that vascular endothelial cells (EC) may contribute to this “factor VIII bypassing activity”. When PCC were incubated with suspensions or monolayer cultures of EC, they acquired the ability to partially bypass the defect of factor VIII deficient plasma. This factor VIII bypassing activity distributed with EC and not with the supernatant PCC, and was not a general property of intravascular cells. The effect of PCC was even more dramatic on fixed EC monolayers, which became procoagulant after incubation with PCC. The time courses of association and dissociation of the PCC-derived factor VIII bypassing activity of fixed and viable EC monolayers were both rapid. We conclude that EC may provide a privileged site for sequestration of constituents of PCC which express coagulant activity and which bypass the abnormality of factor VIII deficient plasma.


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