A Global Experience of Donation after Circulatory Death for Pediatric Lung Transplantation

Hosam F Ahmed1, Kevin Kulshrestha1, Spencer Hogue1

  • 1Department of Cardiothoracic Surgery.

Insights

Pediatric lung transplants using organs from donation after circulatory death (DCD) show similar survival to those from donation after brain death (DBD). This approach supports increasing organ availability for children needing lung transplants.

Area of Science:

  • Pediatric transplantation
  • Thoracic surgery
  • Organ donation

Background:

  • Donation after circulatory death (DCD) is increasingly used for lung transplantation, but data in pediatric recipients is limited.
  • Pediatric lung transplantation faces significant donor organ shortages.

Purpose of the Study:

  • To compare outcomes of pediatric lung transplantation using DCD versus donation after brain death (DBD) organs.
  • To evaluate the feasibility of DCD lung donation in children to address organ shortages.

Main Methods:

  • Analysis of the International Society for Heart and Lung Transplantation (ISHLT) Thoracic Organ Transplant Registry data (2004-2018).
  • Comparison of 34 pediatric DCD lung transplant recipients with 1419 pediatric DBD lung transplant recipients.
  • Use of propensity score matching to create comparable cohorts for outcome analysis.

Main Results:

  • Kaplan-Meier survival and propensity score-matched analyses showed similar post-transplant survival between DCD and DBD pediatric lung transplant recipients (P=0.098).
  • DCD lung transplant recipients experienced a longer post-transplant hospital stay (matched cohort: 26 days vs. 19 days, P=0.016).
  • A trend towards shorter time to acute cellular rejection (ACR) was observed in DCD recipients (matched cohort: 248 days vs. 1650 days, P=0.059).

Conclusions:

  • The study supports the use of DCD for pediatric lung transplantation, potentially increasing donor organ availability for children.
  • Further research is needed to explore the observed shorter time to acute cellular rejection in pediatric DCD lung transplant recipients.