Association of Digoxin Use at Norwood Discharge with Fontan Completion: A Study from the Pediatric Heart Network

Insights

Digoxin use after the Norwood procedure increased the likelihood of Fontan completion in infants with single ventricle heart disease. However, it did not improve transplant-free survival or ventricular function.

Area of Science:

  • Pediatric Cardiology
  • Congenital Heart Disease
  • Cardiac Surgery

Background:

  • Digoxin use post-Norwood procedure is linked to improved interstage survival in hypoplastic left heart syndrome.
  • The long-term impact of digoxin on outcomes in staged palliation for single ventricle heart disease remains unclear.
  • Investigating digoxin's association with transplant-free survival and Fontan completion is crucial.

Purpose of the Study:

  • To determine if digoxin use at Norwood discharge is associated with improved transplant-free survival.
  • To assess the association of digoxin use at Norwood discharge with Fontan completion.
  • To evaluate the impact of digoxin on longer-term outcomes in staged palliation.

Main Methods:

  • Retrospective cohort study using the Pediatric Heart Network (PHN) Single Ventricle Reconstruction trial dataset (n=549).
  • Competing risk analysis for Fontan completion and Cox regression for death/transplant within 6 years.
  • Mixed-effects models compared pre-Fontan hemodynamics and echocardiographic indices, adjusting for covariates.

Main Results:

  • Higher 6-year cumulative incidence of Fontan completion in digoxin users (82% vs 71%, p=0.013).
  • Digoxin users had a greater likelihood of Fontan completion (aHR 1.31; p=0.005), but no significant difference in death/transplant hazard (aHR 0.78; p=0.208).
  • No significant differences in pre-Fontan hemodynamic or echocardiographic indices were observed between groups.

Conclusions:

  • Digoxin use at Norwood discharge is associated with a 30% greater likelihood of Fontan completion by 6 years.
  • This association was not accompanied by improved transplant-free survival or changes in ventricular function.
  • Findings suggest digoxin may facilitate progression through staged palliation for single ventricle heart disease.
Abstract

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