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Direct hyperbilirubinemia in infants with congenital heart disease
Jun Fujishiro1, Masahiko Sugiyama1, Tetsuya Ishimaru1
1Department of Pediatric Surgery, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Insights
Direct hyperbilirubinemia (D-HB) is common in infants with congenital heart disease (CHD) but usually resolves within a week. Clinical factors do not predict D-HB in these infants.
Area of Science:
- Neonatology
- Pediatric Cardiology
- Bilirubin Metabolism
Background:
- Congenital heart disease (CHD) association with infantile cholestasis, crucial for biliary atresia (BA) diagnosis, remains understudied.
- Investigating direct hyperbilirubinemia (D-HB) characteristics in infants with CHD is essential for understanding neonatal jaundice in this population.
Purpose of the Study:
- To characterize direct hyperbilirubinemia (D-HB) in neonates diagnosed with congenital heart disease (CHD).
- To identify potential predictors of D-HB in infants with CHD.
Main Methods:
- Retrospective review of neonates diagnosed with CHD between 2015-2016.
- Analysis of direct hyperbilirubinemia (D-HB) (≥2.0 mg/dL) within 60 days of age and associated clinical parameters.
- Statistical analysis using chi-squared or Wilcoxon rank sum tests.
Main Results:
- 17.1% of 76 infants with CHD exhibited D-HB within 60 days.
- Most D-HB cases (10/13) resolved spontaneously within the hospital stay, 80% within 7 days.
- No association found between D-HB and sex, gestational age, birthweight, chromosomal anomalies, or cardiac surgical status.
Conclusions:
- Direct hyperbilirubinemia (D-HB) is frequently observed in infants with congenital heart disease (CHD) but typically resolves rapidly.
- Neonatal clinical parameters and CHD status do not predict D-HB development.
- Prolonged D-HB (>1 week) in infants with CHD warrants further etiological investigation.
Background:
The association between congenital heart disease (CHD) and infantile cholestasis, a key finding for the diagnosis of biliary atresia (BA), has not been previously investigated. The aim of this study was therefore to investigate the characteristics of direct hyperbilirubinemia (D-HB) in infants with CHD.
Methods:
All neonates admitted to the present hospital and diagnosed with CHD in 2015 and 2016 were included. D-HB (direct bilirubin ≥ 2.0 mg/dL) at ≤60 days of age and other clinical parameters were retrospectively reviewed. Statistical analysis according to presence of D-HB was performed using chi-squared test or Wilcoxon rank sum test.
Results:
Seventy-six patients (M:F, 36:40) were included in this study. CHD consisted of ventricular septal defect in 17, patent ductus arteriosus in 10, and other in 49. Thirteen patients (17.1%) had D-HB at ≤60 days of age. Resolution of D-HB (DB < 2.0 mg/dL) occurred in 10 of the 13 patients during the hospital stay, and this occurred in ≤7 days in eight of the 10 patients. Sex, gestational age, birthweight, chromosomal anomalies, need for Fontan operation for CHD repair, and/or cardiac operation were not associated with D-HB at ≤60 days of age.
Conclusion:
While D-HB was frequently observed in infants with CHD, the majority of D-HB cases resolved spontaneously in ≤1 week. Neonatal clinical parameters or CHD status was not predictive of D-HB. D-HB lasting >1 week in infants with CHD should be evaluated for the cause.
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