2018, Number 6
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Cir Cir 2018; 86 (6)
Remote ischemic preconditioning in liver graft viability
Cordero-Pérez P, Hernández-Guedea M, Jiménez-Pérez JC, Muñoz-Espinosa L, Pérez-Rodríguez E, Zapata-Chavira HA
Language: Spanish
References: 30
Page: 539-547
PDF size: 198.86 Kb.
ABSTRACT
Background: Remote ischemic preconditioning (RIP) in liver transplantation has been suggested experimentally as a strategy
to reduce ischemia-reperfusion injury.
Objective: Evaluate the effect of RIP on liver graft in cadaveric donors and the
impact of various inflammatory mediators in this process.
Method: Ten liver transplantation recipients, 5 controls and 5 PIR,
were made in the cadaver donors by applying a pneumatic tourniquet in the upper third of both thighs for a period of 10 minutes
followed by 10 minutes reperfusion. The determination of interleukine (IL)-1, IL-6, tumor necrosis factor alpha (TNF-α),
vascular endothelial growth factor (VEGF), intracellular adhesion molecule (ICAM)-1 was performed as well as hematological
and biochemical parameters at various stages of liver transplantation.
Results: Significant increase of aspartate aminotransferase
(AST), alanine aminotransferase (ALT) and alkaline phosphatase in the early stages of post-liver transplantation were
observed, after 72 hours subjects who received liver transplantation subjected to RIP they showed a better response, which
was also evident in platelet recovery, which persisted until phase 3 months in this group. IL-6 appears to participate in the early stages of the ischemia-reperfusion injury, contrary to TNF-α that increases until day 7 while ICAM-1 was increased in
all phases.
Conclusions: In this pilot study the PIR decreased the damage by ischemia-reperfusion injury, although the
greatest effect was observed after 72 hours.
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