Risk factors for early invasive fungal infections in paediatric liver transplant recipients

Yehonatan Pasternak1,2, Shiri Rubin1,2, Efraim Bilavsky2,3

  • 1Department of Pediatrics A, Schneider Children's Medical Center, Petach Tikva, Israel.

Mycoses
|April 18, 2018
PubMed

Insights

Invasive fungal infections (IFIs) are common in children after liver transplants, occurring within the first month. Risk factors include multiple blood transfusions and prolonged IV antibiotic use, aiding in early identification of high-risk patients.

Area of Science:

  • Pediatric transplantation immunology
  • Infectious diseases
  • Hepatology

Background:

  • Invasive fungal infections (IFIs) are a significant cause of morbidity and mortality following liver transplantation.
  • Data on IFIs in pediatric liver transplant recipients are limited, particularly concerning early post-transplant outcomes.

Purpose of the Study:

  • To determine the incidence and identify risk factors for IFIs in pediatric liver transplant recipients within the first three months post-transplantation.
  • To develop a predictive model for identifying high-risk pediatric patients for IFIs.

Main Methods:

  • Retrospective analysis of pediatric liver transplant recipients from 2004 to 2014.
  • Stepwise logistic regression was employed to identify independent risk factors for IFIs.
  • A predictive model was formulated using key clinical parameters.

Main Results:

  • Ten IFIs were observed in 81 recipients (12.3%), all within the first month post-transplantation.
  • Candida species, including non-albicans Candida, were the primary causative agents.
  • Significant risk factors identified included multiple blood transfusions, prolonged IV catheter use, extended IV antibiotic treatment, surgical complications, pulse steroid therapy, and living donor liver transplantation.

Conclusions:

  • IFIs represent a substantial early complication in pediatric liver transplant recipients, predominantly occurring within the first month.
  • A predictive model incorporating living donor transplantation and duration of IV antibiotic treatment effectively identifies high-risk patients (AUC 0.918).
  • Further research is warranted to evaluate targeted antifungal prophylaxis strategies for high-risk pediatric liver transplant recipients.

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