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A proposal to grade the severity of early allograft dysfunction after liver transplantation

OBJECTIVE: To propose a grading system for early hepatic graft dysfunction. METHODS: A retrospective study from a single transplant center. Recipients of liver transplants from deceased donors, transplanted under the MELD system were included. Early graft dysfunction was defined by Olthoff criteria....

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Autores principales: Salvalaggio, Paolo, Afonso, Rogerio Carballo, Felga, Guilherme, Ferraz-Neto, Ben-Hur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Israelita de Ensino e Pesquisa Albert Einstein 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872964/
https://www.ncbi.nlm.nih.gov/pubmed/23579740
http://dx.doi.org/10.1590/S1679-45082013000100006
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author Salvalaggio, Paolo
Afonso, Rogerio Carballo
Felga, Guilherme
Ferraz-Neto, Ben-Hur
author_facet Salvalaggio, Paolo
Afonso, Rogerio Carballo
Felga, Guilherme
Ferraz-Neto, Ben-Hur
author_sort Salvalaggio, Paolo
collection PubMed
description OBJECTIVE: To propose a grading system for early hepatic graft dysfunction. METHODS: A retrospective study from a single transplant center. Recipients of liver transplants from deceased donors, transplanted under the MELD system were included. Early graft dysfunction was defined by Olthoff criteria. Multiple cut-off points of post-transplant laboratory tests were used to create a grading system for early graft dysfunction. The primary outcome was 6-months grafts survival. RESULTS: The peak of aminotransferases during the first postoperative week correlated with graft loss. The recipients were divided into mild (aminotransferase peak >2,000IU/mL, but <3,000IU/mL); moderate (aminotransferase peak >3,000IU/mL); and severe (aminotransferase peak >3,000IU/mL + International Normalized Ratio ≥1.6 and/or bilirubin ≥ 10mg/dL in the 7(th) postoperative day) early allograft dysfunction. Moderate and severe early dysfunctions were independent risk factors for graft loss. Patients with mild early dysfunction presented with graft and patient survival comparable to those without graft dysfunction. However, those with moderate early graft dysfunction showed worse graft survival than those who had no graft dysfunction. Patients with severe early dysfunction had graft and patient survival rates worse than those of any other groups. CONCLUSION: Early graft dysfunction can be graded by a simple and reliable criteria based on the peak of aminotransferases during the first postoperative week. The severity of the early graft dysfunction is an independent risk factor for allograft loss. Patients with moderate early dysfunction showed worsening of graft survival. Recipients with severe dysfunction had a significantly worse prognosis for graft and patient survival.
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spelling pubmed-48729642016-08-10 A proposal to grade the severity of early allograft dysfunction after liver transplantation Salvalaggio, Paolo Afonso, Rogerio Carballo Felga, Guilherme Ferraz-Neto, Ben-Hur Einstein (Sao Paulo) Original Article OBJECTIVE: To propose a grading system for early hepatic graft dysfunction. METHODS: A retrospective study from a single transplant center. Recipients of liver transplants from deceased donors, transplanted under the MELD system were included. Early graft dysfunction was defined by Olthoff criteria. Multiple cut-off points of post-transplant laboratory tests were used to create a grading system for early graft dysfunction. The primary outcome was 6-months grafts survival. RESULTS: The peak of aminotransferases during the first postoperative week correlated with graft loss. The recipients were divided into mild (aminotransferase peak >2,000IU/mL, but <3,000IU/mL); moderate (aminotransferase peak >3,000IU/mL); and severe (aminotransferase peak >3,000IU/mL + International Normalized Ratio ≥1.6 and/or bilirubin ≥ 10mg/dL in the 7(th) postoperative day) early allograft dysfunction. Moderate and severe early dysfunctions were independent risk factors for graft loss. Patients with mild early dysfunction presented with graft and patient survival comparable to those without graft dysfunction. However, those with moderate early graft dysfunction showed worse graft survival than those who had no graft dysfunction. Patients with severe early dysfunction had graft and patient survival rates worse than those of any other groups. CONCLUSION: Early graft dysfunction can be graded by a simple and reliable criteria based on the peak of aminotransferases during the first postoperative week. The severity of the early graft dysfunction is an independent risk factor for allograft loss. Patients with moderate early dysfunction showed worsening of graft survival. Recipients with severe dysfunction had a significantly worse prognosis for graft and patient survival. Instituto Israelita de Ensino e Pesquisa Albert Einstein 2013 /pmc/articles/PMC4872964/ /pubmed/23579740 http://dx.doi.org/10.1590/S1679-45082013000100006 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Salvalaggio, Paolo
Afonso, Rogerio Carballo
Felga, Guilherme
Ferraz-Neto, Ben-Hur
A proposal to grade the severity of early allograft dysfunction after liver transplantation
title A proposal to grade the severity of early allograft dysfunction after liver transplantation
title_full A proposal to grade the severity of early allograft dysfunction after liver transplantation
title_fullStr A proposal to grade the severity of early allograft dysfunction after liver transplantation
title_full_unstemmed A proposal to grade the severity of early allograft dysfunction after liver transplantation
title_short A proposal to grade the severity of early allograft dysfunction after liver transplantation
title_sort proposal to grade the severity of early allograft dysfunction after liver transplantation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872964/
https://www.ncbi.nlm.nih.gov/pubmed/23579740
http://dx.doi.org/10.1590/S1679-45082013000100006
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