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


Journal

Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
ISSN: 1527-6473
Titre abrégé: Liver Transpl
Pays: United States
ID NLM: 100909185

Informations de publication

Date de publication:
06 2019
Historique:
received: 01 08 2018
accepted: 02 02 2019
pubmed: 13 2 2019
medline: 11 8 2020
entrez: 13 2 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 30753750
doi: 10.1002/lt.25433
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

911-921

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK109907
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 by the American Association for the Study of Liver Diseases.

Auteurs

Patrick J McKiernan (PJ)

Division of Pediatric Gastroenterology, Hepatology and Nutrition, University of Pittsburgh, Pittsburgh, PA.
Pittsburgh Liver Research Center, University of Pittsburgh, Pittsburgh, PA.

Armando Ganoza (A)

Hillman Center for Pediatric Transplantation, University of Pittsburgh, Pittsburgh, PA.

James E Squires (JE)

Division of Pediatric Gastroenterology, Hepatology and Nutrition, University of Pittsburgh, Pittsburgh, PA.
Pittsburgh Liver Research Center, University of Pittsburgh, Pittsburgh, PA.

Robert H Squires (RH)

Division of Pediatric Gastroenterology, Hepatology and Nutrition, University of Pittsburgh, Pittsburgh, PA.
Pittsburgh Liver Research Center, University of Pittsburgh, Pittsburgh, PA.

Jerry Vockley (J)

Division of Medical Genetics, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, University of Pittsburgh, Pittsburgh, PA.

George Mazariegos (G)

Hillman Center for Pediatric Transplantation, University of Pittsburgh, Pittsburgh, PA.

Kyle Soltys (K)

Hillman Center for Pediatric Transplantation, University of Pittsburgh, Pittsburgh, PA.

Qing Sun (Q)

Hillman Center for Pediatric Transplantation, University of Pittsburgh, Pittsburgh, PA.

Rakesh Sindhi (R)

Hillman Center for Pediatric Transplantation, University of Pittsburgh, Pittsburgh, PA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH