2010
DOI: 10.1007/s00534-010-0344-7
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The effect of methylene blue during orthotopic liver transplantation on post reperfusion syndrome and postoperative graft function

Abstract: In our study, the administration of MB at 1-1.5 mg/kg immediately prior to reperfusion did not prevent post-reperfusion hypotension and did not decrease vasopressor usage or transfusion requirements after reperfusion. Also, MB did not have any impact on postoperative graft function. These findings may argue against the routine use of MB during OLT.

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Cited by 27 publications
(25 citation statements)
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References 39 publications
(66 reference statements)
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“…We rarely use this technique in adult patients at our center because it is time‐consuming and may cause damage to RBCs during the centrifugation process. Many methods, including modified reperfusion techniques, small vasopressor boluses, and adequate volumes before reperfusion, can be used to prevent or treat PRS …”
Section: Discussionmentioning
confidence: 99%
“…We rarely use this technique in adult patients at our center because it is time‐consuming and may cause damage to RBCs during the centrifugation process. Many methods, including modified reperfusion techniques, small vasopressor boluses, and adequate volumes before reperfusion, can be used to prevent or treat PRS …”
Section: Discussionmentioning
confidence: 99%
“…During the pre‐anhepatic stage, the serum potassium level was maintained below 4.0 mEq/L with the intravenous administration of glucose (12.5‐25.0 g) and insulin (5‐10 U) and/or lasix (10‐40 mg). Before the reperfusion of the liver graft, the intravenous administration of sodium bicarbonate (50 mEq), calcium chloride (1000 mg), and methylene blue (100 mg) was performed . The inspiratory oxygen fraction was set at 1.0 before reperfusion.…”
Section: Methodsmentioning
confidence: 99%
“…Most recently, the incidence of PRS has been reported to be approximately 50% . One of the proposed causes of PRS is an increased production of NO . Other potential causes include the response to the release of inflammatory cytokines, particularly tumor necrosis factor α (TNF‐α), from the liver graft, which is known to activate the production of cGMP …”
Section: Discussionmentioning
confidence: 99%