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Do predictors of incomplete Kawasaki disease exist for infants?

Sol Ji No1, Dong Ouk Kim, Kyong Min Choi

  • 1Department of Pediatrics, Kwandong University College of Medicine, Goyang, Korea.

Pediatric Cardiology
|September 25, 2012
PubMed

Insights

Infantile Kawasaki disease (KD) presents unique challenges, often leading to delayed diagnosis. Infants with KD show higher risks of coronary artery issues and diastolic dysfunction, indicated by elevated Pro-BNP and specific echocardiographic findings.

Area of Science:

  • Pediatrics
  • Cardiology
  • Rheumatology

Background:

  • Kawasaki disease (KD) is a leading cause of acquired heart disease in children.
  • Diagnosis of infantile KD can be challenging due to nonspecific symptoms.
  • Early identification is crucial to prevent cardiac complications.

Purpose of the Study:

  • To evaluate clinical characteristics and cardiac complications in infants with KD.
  • To compare infantile KD with that in older children.
  • To identify markers for early diagnosis of incomplete KD in infants.

Main Methods:

  • Retrospective review of 242 KD patients.
  • Categorization into infants (≤12 months) and older children (>12 months).
  • Analysis of clinical, laboratory, and echocardiographic data, including Pro-BNP and tissue Doppler imaging.

Main Results:

  • Incomplete KD was more frequent in infants.
  • Infants exhibited higher Pro-hormone Brain Natriuretic Peptide (Pro-BNP) levels and thrombocytosis.
  • Infants showed increased coronary artery z-scores and higher E/E' ratios on tissue Doppler imaging, indicating diastolic dysfunction.

Conclusions:

  • Infants with KD face a higher risk of coronary abnormalities and diastolic dysfunction.
  • Elevated Pro-BNP, thrombocytosis, and specific echocardiographic parameters (higher E/E' ratio) can aid in diagnosing incomplete KD in infants.