Ischemic pre-conditioning in deceased donor liver transplantation:: A prospective randomized clinical trial

被引:100
作者
Amador, A. [1 ]
Grande, L.
Marti, J.
Deulofeu, R.
Miquel, R.
Sola, A.
Rodriguez-Laiz, G.
Ferrer, J.
Fondevila, C.
Charco, R.
Fuster, J.
Hotter, G.
Garcia-Valdecasas, J. C.
机构
[1] Hosp Sabadell, Consorci Sanitari Parc Tauli, Hepato Biliary Pancreat Surg Unit, Barcelona, Spain
[2] Hosp del Mar, Dept Surg, Barcelona, Spain
[3] CSIC, IIBB, Inst Invest Biomed August Pi Sunyer, Dept Expt Pathol, Barcelona, Spain
[4] Mt Sinai Med Ctr, Recanati Miller Tranplantat Inst, Miami Beach, FL 33140 USA
关键词
apoptosis; clinical application; cold ischemia; graft function; ischemia/reperfusion injury; initial poor function; ischemic preconditioning; liver transplantation; primary nonfunction liver; transplantation research;
D O I
10.1111/j.1600-6143.2007.01914.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
To assess the immediate and long-term effects of ischemic preconditioning (IPC) in deceased donor. liver transplantation (LT), we designed a prospective, randomized controlled trial involving 60 donors: control group (CTL, n = 30) or study group (IPC, n = 30). IPC was induced by 10-min hiliar clamping immediately before recovery of organs. Clinical data and blood and liver samples were obtained in the donor and in the recipient for measurements. IPC significantly improved biochemical markers of liver cell function such as uric acid, hyaluronic acid and Hypoxia-Induced Factor-1alpha (HIF-1 alpha) levels. Moreover, the degree of apoptosis was significantly lower in the IPC group. On clinical basis, IPC significantly improved the serum aspartate aminotransferase (AST) levels and reduced the need for reoperation in the postoperative period. Moreover, the incidence of primary nonfunction (PNF) was lower in the IPC group, but did not achieve statistical significance. We conclude that 10-min IPC protects against I/R injury in deceased donor LT.
引用
收藏
页码:2180 / 2189
页数:10
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