Conjugated hyperbilirubinemia is associated with increased morbidity and mortality after neonatal heart surgery

Mallory Hunt1, Iris E M de Jong2, Rebecca G Wells2

  • 1Division of Cardiothoracic Surgery, Department of Surgery, Children's Hospital of Philadelphia and the Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Cardiology in the Young
|December 18, 2023
PubMed

Insights

Conjugated hyperbilirubinemia after neonatal heart surgery is linked to increased complications and mortality. This condition, affecting 8.5% of patients, indicates a need for further investigation into its underlying mechanisms.

Area of Science:

  • Neonatal Cardiology
  • Pediatric Hepatology
  • Critical Care Medicine

Background:

  • Cholestasis, marked by conjugated hyperbilirubinemia, signifies hepatobiliary dysfunction in neonates post-cardiac surgery.
  • Understanding its incidence and impact is crucial for improving outcomes in this vulnerable population.

Purpose of the Study:

  • To determine the incidence of conjugated hyperbilirubinemia following neonatal heart surgery.
  • To investigate the association between conjugated hyperbilirubinemia and post-operative morbidity and mortality.

Main Methods:

  • Retrospective analysis of neonates undergoing congenital heart disease (CHD) surgery (2010-2020).
  • Defined conjugated hyperbilirubinemia as perioperative conjugated bilirubin > 1 mg/dL.
  • Utilized Kaplan-Meier survival analysis for in-hospital mortality.

Main Results:

  • Conjugated hyperbilirubinemia occurred in 8.5% of patients.
  • Associated with younger gestational age, lower birth weight, non-Caucasian race, chromosomal/non-cardiac anomalies, and pre-operative ECMO.
  • Increased in-hospital mortality (OR 5.4) and post-operative complications; 1-year survival was 6% for bilirubin levels >10 mg/dL.

Conclusions:

  • Conjugated hyperbilirubinemia is a significant predictor of post-operative complications and reduced survival post-neonatal heart surgery.
  • Higher incidence in neonates with chromosomal and non-cardiac anomalies warrants further mechanistic research.
Abstract