Literature DB >> 30753750

Evolving Trends in Liver Transplant for Metabolic Liver Disease in the United States.

Patrick J McKiernan1,2, Armando Ganoza3, James E Squires1,2, Robert H Squires1,2, Jerry Vockley4, George Mazariegos3, Kyle Soltys3, Qing Sun3, Rakesh Sindhi3.   

Abstract

Indications for liver transplantation (LT) in metabolic disease are evolving. We reviewed the US experience with primary LT for metabolic disease in the Scientific Registry for Transplant Recipients (October 1987 to June 2017) to determine the following: temporal changes in indications, longterm outcomes, and factors predicting survival. Patients were grouped by the presence of structural liver disease (SLD) and whether the defect was confined to the liver. There were 5996 patients who underwent LT for metabolic disease, 2354 (39.3%) being children. LT for metabolic disease increased in children but not in adults. Children experienced a 6-fold increase in LT for metabolic disease without SLD. Indications for LT remained stable in adults. Living donor liver transplantation increased between era 1 and era 3 from 5.6% to 7.6% in children and 0% to 4.5% in adults. Patient and graft survival improved with time. The latest 5-year patient survival rates were 94.5% and 81.5% in children and adults, respectively. Outcomes were worse in adults and in those with extrahepatic disease (P < 0.01), whereas SLD did not affect outcomes. Survival improved with younger age at LT until age <2 years. On multivariate analysis, diagnostic category, inpatient status, age at LT, and transplant era significantly predicted outcomes in all ages with male sex predicting survival in childhood only. Children without structural disease were less likely to die awaiting LT and had improved post-LT survival compared with children with chronic liver disease. In conclusion, LT for metabolic disease is increasingly used for phenotypic correction in children; extrahepatic manifestations significantly impact survival at all ages; where indicated, transplantation should not be unnecessarily delayed; and the development of new allocation models may be required.
Copyright © 2019 by the American Association for the Study of Liver Diseases.

Entities:  

Year:  2019        PMID: 30753750     DOI: 10.1002/lt.25433

Source DB:  PubMed          Journal:  Liver Transpl        ISSN: 1527-6465            Impact factor:   5.799


  2 in total

1.  Domino hepatocyte transplantation using explanted human livers with metabolic defects attenuates D-GalN/LPS-induced acute liver failure.

Authors:  Guang-Peng Zhou; Shi-Peng Li; Yi-Zhou Jiang; Jie Sun; Yu-Le Tan; Zhi-Gui Zeng; Lin Wei; Wei Qu; Li-Ying Sun; Zhi-Jun Zhu
Journal:  J Transl Med       Date:  2022-10-20       Impact factor: 8.440

2.  Ethylmalonic encephalopathy and liver transplantation: long-term outcome of the first treated patient.

Authors:  Giorgia Olivieri; Diego Martinelli; Daniela Longo; Chiara Grimaldi; Daniela Liccardo; Ivano Di Meo; Andrea Pietrobattista; Anna Sidorina; Michela Semeraro; Carlo Dionisi-Vici
Journal:  Orphanet J Rare Dis       Date:  2021-05-19       Impact factor: 4.123

  2 in total

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