Cross-Circulation for Extracorporeal Liver Support in a Swine Model

被引:6
|
作者
Wu, Wei Kelly [1 ,2 ]
Tumen, Andrew [1 ]
Stokes, John W. [1 ]
Ukita, Rei [1 ]
Hozain, Ahmed [3 ,4 ]
Pinezich, Meghan [4 ]
O'Neill, John D. [4 ,5 ]
Lee, Michael J. [6 ]
Reimer, Jonathan A. [3 ,4 ]
Flynn, Charles R. [7 ]
Talackine, Jennifer R. [1 ]
Cardwell, Nancy L. [1 ]
Benson, Clayne [8 ]
Vunjak-Novakovic, Gordana [4 ,9 ]
Alexopoulos, Sophoclis P. [2 ]
Bacchetta, Matthew [1 ,10 ,11 ]
机构
[1] Vanderbilt Univ, Dept Thorac Surg, Med Ctr, 609 Oxford House,1313 21st Ave South, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Surg, Div Hepatobiliary Surg & Liver Transplantat, Med Ctr, 801 Oxford House,1313 21st Ave South, Nashville, TN 37232 USA
[3] Columbia Univ, Dept Surg, Med Ctr, New York, NY USA
[4] Columbia Univ, Dept Biomed Engn, New York, NY USA
[5] SUNY Downstate Med Ctr, Dept Cell Biol, Brooklyn, NY 11203 USA
[6] Columbia Univ, Dept Pathol & Cell Biol, Med Ctr, New York, NY USA
[7] Vanderbilt Univ, Dept Surg, Med Ctr, Nashville, TN 37232 USA
[8] Vanderbilt Univ, Dept Anesthesiol, Med Ctr, Nashville, TN 37232 USA
[9] Columbia Univ, Dept Med, New York, NY USA
[10] Vanderbilt Univ, Dept Cardiac Surg, Med Ctr, 609 Oxford House,1313 21st Ave South, Nashville, TN 37232 USA
[11] Vanderbilt Univ, Dept Biomed Engn, Nashville, TN 37232 USA
关键词
liver transplantation; normothermic machine perfusion; organ preservation; ex vivo organ support; POSTREPERFUSION SYNDROME; WARM ISCHEMIA; PRESERVATION; TRANSPLANTATION; REPERFUSION; BIOPSIES;
D O I
10.1097/MAT.0000000000001543
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Although machine perfusion has gained momentum as an organ preservation technique in liver transplantation, persistent organ shortages and high waitlist mortality highlight unmet needs for improved organ salvage strategies. Beyond preservation, extracorporeal organ support platforms can also aid the development and evaluation of novel therapeutics. Here, we report the use of veno-arterial-venous (V-AV) cross-circulation (XC) with a swine host to provide normothermic support to extracorporeal livers. Functional, biochemical, and morphological analyses of the extracorporeal livers and swine hosts were performed over 12 hours of support. Extracorporeal livers maintained synthetic function through alkaline bile production and metabolic activity through lactate clearance and oxygen consumption. Beyond initial reperfusion, no biochemical evidence of hepatocellular injury was observed. Histopathologic injury scoring showed improvements in sinusoidal dilatation and composite acute injury scores after 12 hours. Swine hosts remained hemodynamically stable throughout XC support. Altogether, these outcomes demonstrate the feasibility of using a novel V-AV XC technique to provide support for extracorporeal livers in a swine model. V-AV XC has potential applications as a translational research platform and clinical biotechnology for donor organ salvage.
引用
收藏
页码:561 / 570
页数:10
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