2003
DOI: 10.1097/01.tp.0000071205.52835.a4
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Use of steatotic graft in living-donor liver transplantation

Abstract: In conclusion, the use of a fatty liver graft up to the moderate level can be justified in LDLT, even though ischemia-reperfusion injury tends to be severe in such grafts.

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Cited by 117 publications
(92 citation statements)
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“…Most of the previous studies on the quality assessment of donated liver tissue were performed with a routine histopathological procedure on organs from both living and cadaveric donors. [2][3][4] In other reports on large series of pretransplant liver biopsies, the method used for the histological analysis was not specified. 5,6 The frozen-section approach implies lower histopathological definition but allows a rapid histological examination.…”
mentioning
confidence: 99%
“…Most of the previous studies on the quality assessment of donated liver tissue were performed with a routine histopathological procedure on organs from both living and cadaveric donors. [2][3][4] In other reports on large series of pretransplant liver biopsies, the method used for the histological analysis was not specified. 5,6 The frozen-section approach implies lower histopathological definition but allows a rapid histological examination.…”
mentioning
confidence: 99%
“…However, there are little clear parameters to demonstrate the limits of the fatty liver. It was reported that in the LDLT the fatty liver was acceptable to the moderate grade of macrovesicular steatosis (20-50% of macrovesicular steatosis) [18]. However, recent research has showed that the breakdown of sinusoidal reconstitution occurs in the liver regeneration process of a fatty liver [19]; therefore, the fatty liver donor should be avoided in the case of the small-for-size graft.…”
Section: Donor Fatty Livermentioning
confidence: 99%
“…66 However, MiS is frequently regarded as a mild and reversible condition and is usually disregarded as a risk factor for graft dysfunction, it has been established that graft MiS is an independent factor influencing the early graft function (EGD). 61 Cieslak et al 67 observed that a 12% increase in MiS was equivalent to a 50% increased risk for graft dysfunction. 67 MiS may develop because of severe and prolonged inhibition of mitochondrial β-oxidation of FAs during preservation-reperfusion injury.…”
Section: Impact Of Steatosis On Ltmentioning
confidence: 99%
“…69 On the contrary and despite the graft dysfunction risk, the use of livers exhibiting MiS does not decrease graft or patient survival rates. 61 On the other hand, the composition of hepatic lipids and particularly thromboxane A 2 levels are considered the principal modulators of I/R injury in the steatotic livers, while the size and morphology of lipid droplets are insignificant. 70 Other potential mechanisms that have been proposed include Kupffer cell dysfunction, 71 more lipid peroxidation, 72,73 more exuberant pro-inflammatory responses, including increased release of pro-inflammatory mediators such as TNF-α, 74 and impaired leukocyte adhesion.…”
Section: Impact Of Steatosis On Ltmentioning
confidence: 99%
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