Prediction of Graft Survival Post-liver Transplantation by L-GrAFT Risk Score Model, EASE Score, MEAF Scoring, and EAD
Background: Early allograft dysfunction (EAD) is correlated with poor patient or graft survival in liver transplantation. However, the power of distinct definitions of EAD in prediction of graft survival is unclear. Methods: This retrospective, single-center study reviewed data of 677 recipients und...
Saved in:
Published in | Frontiers in surgery Vol. 8; p. 753056 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
19.11.2021
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Background:
Early allograft dysfunction (EAD) is correlated with poor patient or graft survival in liver transplantation. However, the power of distinct definitions of EAD in prediction of graft survival is unclear.
Methods:
This retrospective, single-center study reviewed data of 677 recipients undergoing orthotopic liver transplant between July 2015 and June 2020. The following EAD definitions were compared: liver graft assessment following transplantation (L-GrAFT) risk score model, early allograft failure simplified estimation score (EASE), model for early allograft function (MEAF) scoring, and Olthoff criteria. Risk factors for L-GrAFT
7
high risk group were evaluated with univariate and multivariable logistic regression analysis.
Results:
L-GrAFT
7
had a satisfied C-statistic of 0.87 in predicting a 3-month graft survival which significantly outperformed MEAF (C-statistic = 0.78,
P
= 0.01) and EAD (C-statistic = 0.75,
P
< 0.001), respectively. L-GrAFT
10
, EASE was similar to L-GrAFT
7
, and they had no statistical significance in predicting survival. Laboratory model for end-stage liver disease score and cold ischemia time are risk factors of L-GrAFT
7
high-risk group.
Conclusion:
L-GrAFT
7
risk score is capable for better predicting the 3-month graft survival than the MEAF and EAD in a Chinese cohort, which might standardize assessment of early graft function and serve as a surrogate endpoint in clinical trial. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Alfonso Avolio, Catholic University of the Sacred Heart, Italy Reviewed by: Alessandro Vitale, University Hospital of Padua, Italy; Vatche Agopian, UCLA David Geffen School of Medicine, United States This article was submitted to Visceral Surgery, a section of the journal Frontiers in Surgery These authors have contributed equally to this work and share first authorship |
ISSN: | 2296-875X 2296-875X |
DOI: | 10.3389/fsurg.2021.753056 |