Changes in waiting time, need for mechanical circulatory support and outcomes in paediatric heart transplant

Lisa-Maria Rosenthal1,2,3, Annemarie Krauss1, Oliver Miera1

  • 1Department of Congenital Heart Disease-Pediatric Cardiology, Deutsches Herzzentrum der Charité, Berlin, Germany.

ESC Heart Failure
|July 15, 2024
PubMed

Insights

Paediatric heart transplantation survival has significantly improved over 35 years, with better outcomes despite increased waiting times and mechanical circulatory support (MCS) use. These advancements ensure favourable long-term results for young heart failure patients.

Area of Science:

  • Cardiology
  • Pediatric Surgery
  • Transplantation Medicine

Background:

  • Heart transplantation is a critical treatment for pediatric end-stage heart failure.
  • Excellent long-term outcomes are achievable in pediatric heart recipients.

Purpose of the Study:

  • To analyze trends in pediatric heart transplantation over 35 years.
  • To evaluate changes in diagnoses, survival rates, waiting times, and mechanical circulatory support (MCS) utilization.
  • To assess the impact of these changes on patient outcomes.

Main Methods:

  • Retrospective analysis of 244 pediatric heart transplant recipients (<18 years) from 1986-2022.
  • Data divided into three decades: 1991-2000, 2001-2010, and 2011-2020.
  • Examination of survival, waiting times, and MCS use over time.

Main Results:

  • 1-year survival improved from 79.3% to 92.3% (P=0.041) over the study period.
  • Median overall survival reached 18.0 years; conditional survival at 1 year was 20.9 years.
  • Increased waiting times, particularly for younger children, and a surge in MCS (VAD) use (67% in the last decade) were observed, yet survival remained favorable.

Conclusions:

  • Pediatric heart transplant outcomes show continuous improvement.
  • Increased demand for organs and reliance on VADs as a bridge to transplantation do not compromise post-transplant survival.
  • Long-term results remain favorable despite evolving challenges in pediatric heart transplantation.
Abstract