Pediatric discard risk index for predicting pediatric liver allograft discard

Tahir Malik1, Manasi Joshi1, Elizabeth Godfrey1

  • 1Department of Surgery, Baylor College of Medicine, Houston, TX, USA.

Insights

A new pediatric discard risk score (pDSRI) predicts liver allograft discard using 11 factors, aiming to reduce waste and optimize donor supply for children awaiting transplants.

Area of Science:

  • Organ transplantation
  • Pediatric hepatology
  • Transplant immunology

Background:

  • Annually, 600 pediatric candidates are listed for liver transplants, with 100 remaining on the waiting list.
  • Over 100 pediatric liver allografts are discarded yearly, frequently due to subjective assessments.
  • This represents a significant loss of viable organs and a challenge in optimizing donor supply.

Purpose of the Study:

  • To develop a predictive risk index for pediatric liver allograft discard.
  • To optimize the utilization of donor organs for pediatric liver transplantation.
  • To reduce the number of discarded liver allografts by providing objective discard criteria.

Main Methods:

  • Retrospective analysis of 17,367 deceased pediatric donors (≤18 years old) using the UNOS database.
  • Development of a risk index (pDSRI) through univariate and multivariate logistic regression models.
  • Identification of significant predictors of allograft discard based on clinical and laboratory data.

Main Results:

  • Eleven significant predictors of pediatric liver allograft discard were identified (P < .05).
  • Key risk factors included donation after cardiac death (DCD), total bilirubin >10 mg/dL, and alanine transaminase (ALT) ≥500 IU/L.
  • The pDSRI demonstrated strong predictive accuracy with a C-statistic of 0.846 (training) and 0.840 (validation).

Conclusions:

  • The pDSRI accurately predicts the risk of pediatric liver allograft discard.
  • This tool incorporates 11 significant risk factors, including liver function tests and donor characteristics.
  • The pDSRI can potentially maximize donor yield and improve organ allocation for pediatric liver transplantation.
Abstract

Related Concept Videos

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test01:22

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

In clinical practice, the direct measurement of hepatic blood flow to evaluate liver function presents significant challenges due to the intricate and specialized nature of the necessary techniques. Consequently, healthcare professionals often rely on empirical estimates derived from thorough patient examinations and liver function tests to gauge liver health. Among the tools at their disposal, the Child–Pugh and MELD scoring systems stand out for their ability to categorize and assess...
82
Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
109
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
132
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
109
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
89
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
107