Outcomes of Children Supported With Pulsatile Paracorporeal Ventricular Assist Device: Congenital Versus Acquired

Mark S Bleiweis1, Joseph Philip1, Yuriy Stukov1

  • 1Congenital Heart Center, Departments of Surgery, Pediatrics, and Anesthesiology, University of Florida, Gainesville, FL, USA.

Insights

Pediatric patients with congenital heart disease (CHD) show lower survival rates after ventricular assist device (VAD) implantation compared to those with acquired heart disease (AHD). Pulsatile VADs are crucial for bridge-to-transplantation in CHD, but outcomes remain poorer.

Area of Science:

  • Pediatric Cardiology
  • Cardiovascular Surgery
  • Biomedical Engineering

Background:

  • Ventricular assist devices (VADs) are used in pediatric patients with end-stage heart failure.
  • Comparison of VAD outcomes between congenital heart disease (CHD) and acquired heart disease (AHD) is critical for optimizing treatment strategies.
  • This study evaluates the Berlin Heart VAD outcomes in 82 pediatric patients, stratifying by CHD and AHD.

Approach:

  • Retrospective review of 82 pediatric patients (<18 years) receiving Berlin Heart VAD support.
  • Patients were categorized into congenital heart disease (CHD, n=44) and acquired heart disease (AHD, n=37) groups.
  • Kaplan-Meier survival analysis and log-rank tests were employed to compare long-term outcomes.

Key Points:

  • One-year survival was significantly lower in CHD patients (59.9%) compared to AHD patients (88.6%) (P=.0004).
  • Five-year survival also showed a significant difference, with 55.4% for CHD versus 85.3% for AHD (P=.002).
  • While VADs facilitate bridge-to-transplantation in CHD, survival rates remain a significant challenge compared to AHD.

Conclusions:

  • Pulsatile VADs are essential for bridge-to-transplantation in pediatric patients with CHD.
  • Survival outcomes following VAD insertion are demonstrably worse in children with CHD compared to those with AHD.
  • Further research and therapeutic advancements are needed to improve VAD efficacy and long-term survival in pediatric CHD.
Abstract