Clinical course of infants with congenital heart disease who developed thyroid dysfunction within 100 days

Hye Jin Lee1, Hyeoh Won Yu2, Gi Beom Kim2

  • 1Department of Pediatrics, Hallym University Kangnam Sacred Heart Hospital, Seoul, Korea.

Insights

Thyroid dysfunction is common in infants with congenital heart disease (CHD), affecting two-thirds of those screened. Transient dysfunction was more frequent, highlighting the need for revised thyroid function test (TFT) screening criteria in these vulnerable infants.

Area of Science:

  • Pediatric Endocrinology
  • Neonatal Cardiology
  • Thyroidology

Background:

  • Congenital heart disease (CHD) presents unique challenges for neonatal care.
  • Thyroid dysfunction can complicate the clinical course of infants with CHD.
  • Neonatal screening tests (NSTs) may not detect all thyroid abnormalities in CHD infants.

Purpose of the Study:

  • To investigate the incidence and clinical course of thyroid dysfunction in infants with CHD within 100 days of birth.
  • To identify potential risk factors associated with thyroid dysfunction in this population.
  • To evaluate the effectiveness of current screening protocols.

Main Methods:

  • Retrospective review of 54 infants with CHD who underwent thyroid function tests (TFTs).
  • Data collection included birth history, CHD diagnosis, genetic abnormalities, medications, surgeries, and exposure to iodine contrast media (ICM).
  • Analysis of neonatal screening tests (NSTs) and TFT results.

Main Results:

  • Thyroid dysfunction was observed in 36 out of 54 (66.7%) infants, with 53.7% transient and 13.0% permanent.
  • Infants with transient dysfunction had lower birth weight and higher exposure to thyroid-disrupting medications/ICM, though not statistically significant.
  • Eight patients exposed to ICM showed thyroid dysfunction, with five recovering from transient forms.

Conclusions:

  • Thyroid dysfunction is prevalent in CHD infants, often occurring despite normal NSTs.
  • Risk factors like ICM exposure and medication require further investigation.
  • Larger studies are needed to refine TFT screening guidelines for CHD infants.
Abstract

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