Bilirubin Removal by Plasmafiltration-Adsorption: Ex vivo Adsorption Kinetics Model and Single Case Report

被引:1
|
作者
Marcello, Matteo [1 ,2 ]
Lorenzin, Anna [1 ,3 ]
De Cal, Massimo [1 ,3 ]
Zorzi, Michela [4 ]
La Malfa, Marco Salvatore [4 ]
Fin, Valentina [4 ]
Sandini, Alessandra [5 ]
Fiorin, Francesco [5 ]
Bellomo, Rinaldo [6 ,7 ,8 ,9 ]
De Rosa, Silvia [10 ]
Ronco, Claudio [1 ,3 ]
Zanella, Monica [1 ,3 ]
机构
[1] Int Renal Res Inst Vicenza, Vicenza, Italy
[2] Univ Vita Salute San Raffaele, Milan, Italy
[3] St Bortolo Hosp, Dept Nephrol Dialysis & Transplantat, Vicenza, Italy
[4] St Bortolo Hosp, Dept Pharm, Vicenza, Italy
[5] St Bortolo Hosp, Dept Transfus Med, Vicenza, Italy
[6] Austin Hosp, Dept Intens Care, Melbourne, Vic, Australia
[7] Monash Univ, Australian & New Zealand Intens Care Res Ctr, Melbourne, Vic, Australia
[8] Univ Melbourne, Dept Crit Care, Melbourne, Vic, Australia
[9] Royal Melbourne Hosp, Dept Intens Care, Melbourne, Vic, Australia
[10] St Bortolo Hosp, Dept Intens Care, Vicenza, Italy
关键词
Bilirubin; Adsorption; BS330; Plasmafiltration-adsorption; HYPERBILIRUBINEMIA;
D O I
10.1159/000528062
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Extracorporeal removal of bilirubin in patients with severe liver dysfunction is a key blood purification strategy. We conducted an ex vivo study to assess the quantitative capacity to remove bilirubin from plasma of a novel adsorptive cartridge. Methods: We studied a downscaled module of the BS330 Plasma Bilirubin Adsorption Column Cartridge (Jafron Biomedical, Zhuhai City, China) to minimize the plasma requirement in an ex vivo circulation using a solution of hyperbilirubinemic plasma. We measured the bilirubin concentration gap (Delta C) between inlet (Cp-in) and outlet (Cp-out) of the unit and we calculated the removal ratio (RR) as mass adsorbed at different time points. Moreover, we compared the ex vivo model with the bilirubin adsorption kinetics in a patient with acute on chronic liver failure treated with the BS330 cartridge. Results: Bilirubin concentration change across the cartridge at 30 min was 16.5%, and cartridge saturation was reached at 750 min. We used a minimodule downscaled to 1:3 and containing approximately 131 g of BS330 sorbent beads: the device retained 759 mg of bilirubin with a RR of 78.1% and a RR of 42.6% at 120 min. Thus, the adsorption capacity was 5.76 mg of bilirubin per gram of sorbent. Bilirubin adsorption kinetics in our clinical case with a full-scale unit shows a coherent trend with a total bilirubin mass adsorbed after 180 min of 470 mg. Discussion: Our findings provide the first assessment of bilirubin adsorption in an ex vivo model of plasma perfusion and can be used to design interventional studies in humans, providing guidance for an adequate prescription of treatment frequency and duration.
引用
收藏
页码:345 / 351
页数:7
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