Literature DB >> 28199762

Improving the Diagnostic Criteria for Primary Liver Graft Nonfunction in Adults Utilizing Standard and Transportable Laboratory Parameters: An Outcome-Based Analysis.

M A B Al-Freah1, M J W McPhail1, E Dionigi1, M R Foxton1, G Auzinger1, M Rela1, J A Wendon1, J G O'Grady1, M A Heneghan1, N D Heaton1, W Bernal1.   

Abstract

Current diagnostic criteria for primary nonfunction (PNF) of liver grafts are based on clinical experience rather than statistical methods. A retrospective, single-center study was conducted of all adults (n = 1286) who underwent primary liver transplant (LT) 2000-2008 in our center. Laboratory variables during the first post LT week were analyzed. Forty-two patients (3.7%) had 2-week graft failure. Transplant albumin, day-1 aspartate aminotransferase (AST), day-1 lactate, day-3 bilirubin, day-3 international normalized ratio (INR), and day-7 AST were independently associated with PNF on multivariate logistic regression. PNF score =(0.000280*D1AST)+ (0.361*D1 Lactate)+(0.00884*D3 Bilirubin)+(0.940*D3 INR)+(0.00153*D7 AST)-(0.0972*TxAlbumin)-4.5503. Receiver operating curve analysis showed the model area under receiver operating curve (AUROC) of 0.912 (0.889-0.932) was superior to the current United Kingdom (UK) PNF criteria of 0.669 (0.634-0.704, p < 0.0001). When applied to a validation cohort (n = 386, 34.4% patients), the model had AUROC of 0.831 (0.789-0.867) compared to the UK early graft dysfunction criteria of 0.674 (0.624-0.721). The new model performed well after exclusion of patients with marginal grafts and when modified to include variables from the first three post-LT days only (AUROC of 0.818, 0.776-0.856, p = 0.001). This model is superior to the current UK PNF criteria and is based on statistical methods. The model is also applicable to recipients of all types of grafts (marginal and nonmarginal).
© 2017 The American Society of Transplantation and the American Society of Transplant Surgeons.

Entities:  

Keywords:  clinical research/practice; liver allograft function/dysfunction; liver transplantation/hepatology; liver transplantation: auxiliary; liver transplantation: living donor; liver transplantation: split

Mesh:

Year:  2017        PMID: 28199762     DOI: 10.1111/ajt.14230

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  2 in total

1.  Association Between Serum Lactate and Unsatisfactory Outcomes in Critically Ill Children in the Immediate Post-operative Period of Liver Transplantation.

Authors:  Jaime Fernández-Sarmiento; María Angélica Wilches-Cuadros; Ricardo Hernandez-Sarmiento; Hernando Mulett; Karen Moreno-Medina; Nicolás Molano; Julián Augusto Palomar Dominguez; Lorena Acevedo; Claudia Salinas; Jairo Rivera
Journal:  Front Pediatr       Date:  2022-01-24       Impact factor: 3.418

2.  Procalcitonin in early allograft dysfunction after orthotopic liver transplantation: a retrospective single centre study.

Authors:  Katja Frick; Elisabeth A Beller; Marit Kalisvaart; Philipp Dutkowski; Reto A Schüpbach; Stephanie Klinzing
Journal:  BMC Gastroenterol       Date:  2022-08-31       Impact factor: 2.847

  2 in total

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