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Echocardiographic findings in mild and severe forms of sickle cell anemia

Y Kilinç1, E Acartürk, M Kümi

  • 1Department of Pediatric Hematology, Cukurova University Medical Faculty, Balcali, Adana, Turkey.

Acta Paediatrica Japonica : Overseas Edition
|June 1, 1993
PubMed

Insights

M-mode echocardiography reveals enlarged left heart chambers in children with sickle cell anemia, regardless of disease severity. Despite volume overload, cardiac systolic function remains normal in affected children.

Area of Science:

  • Pediatric Cardiology
  • Hematology
  • Medical Imaging

Background:

  • Sickle cell anemia (SCA) is a genetic blood disorder with potential cardiac complications.
  • Echocardiography is crucial for assessing cardiac structure and function in pediatric patients.

Purpose of the Study:

  • To compare M-mode echocardiographic findings between children with sickle cell anemia and healthy controls.
  • To investigate potential cardiac structural changes associated with SCA severity.

Main Methods:

  • M-mode echocardiography was performed on 30 children with SCA (12 mild, 18 severe) and 12 healthy children.
  • Echocardiographic parameters including left atrium dimension, left ventricle dimensions, posterior wall thickness, and fractional shortening were analyzed.

Main Results:

  • Children with SCA, both mild and severe, exhibited increased left atrium and left ventricle end-diastolic dimensions compared to controls.
  • Posterior left ventricle thickness and left ventricle mass were also elevated in SCA groups.
  • Left ventricular fractional shortening and systolic function remained normal despite cardiac volume load and dilatation.

Conclusions:

  • Sickle cell anemia is associated with significant cardiac chamber enlargement, particularly the left atrium and left ventricle.
  • Cardiac systolic function is preserved in pediatric SCA patients despite echocardiographic evidence of volume overload.
  • Echocardiographic findings did not correlate with hematological indices in this cohort.

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