4.5 Article

Nomograms for Predicting the Incidence of Late-Onset Acute Cellular Rejection in Patients After Pediatric Liver Transplantation

Journal

FRONTIERS IN PEDIATRICS
Volume 10, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fped.2022.915795

Keywords

late-onset acute cellular rejection; pediatric liver transplantation; nomogram; individualized prediction; risk factors

Categories

Funding

  1. Tianjin Key Medical Discipline (Specialty) Construction Project, National Natural Science Foundation of China [82170672]
  2. Tianjin First Central Hospital Spring Plan [2020CF23]
  3. Project ELITE: A Special Supportive Program for Organ Transplantation by COTDF [2019JYJH03]

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This study aimed to explore and predict the incidence of late-onset acute cellular rejection (LACR) after pediatric liver transplantation (pLT). The study found that cold ischemia time, donor-specific antibodies (DSAs), and tacrolimus concentration were independent influencing factors for LACR. Two prediction models were established to predict the incidence of LACR after 1-2 years and more than 2 years of pLT.
BackgroundLate-onset acute cellular rejection (LACR) is a special type of acute rejection (AR) only rarely studied after pediatric liver transplantation (pLT). Our study aimed to explore the influencing factors of LACR after pLT and establish a nomogram to provide an individualized prediction of LACR after pLT. Materials and MethodsData from 640 children who underwent pLT at Tianjin First Central Hospital from January 2016 to December 2019 were collected as part of this retrospective study. The nomogram was then established through the results of the multivariable analysis. ResultsForty-one patients experienced LACR > 1 <= 2 years after pLT. Cold ischemia time, donor-specific antibodies (DSAs), and tacrolimus concentration were independent influencing factors, and a nomogram was established with an AUC value of 0.834 (95% confidence interval, 0.755-0.912). Ten-fold cross-validation showed that the accuracy of the nomogram was about 76%. Sixty-three patients experienced LACR > 2 years after pLT. Child-Pugh grade, cold ischemic time, DSAs, early acute cellular rejection, and tacrolimus concentration were independent influencing factors, and a nomogram was established with an AUC value of 0.827 (95% confidence interval, 0.774-0.881). Ten-fold cross-validation showed that the accuracy of the nomogram was about 80.9%. ConclusionWe established nomograms to predict the incidence of LACR > 1 <= 2 and > 2 years after pLT, respectively. The verification results showed that nomograms had good accuracy and clinical practicability.

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