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Coarctation of the aorta: difficulties in prenatal diagnosis

G K Sharland1, K Y Chan, L D Allan

  • 1Department of Fetal Cardiology, Guy's Hospital, London.

British Heart Journal
|January 1, 1994
PubMed

Insights

Prenatal diagnosis of coarctation of the aorta is challenging. While aortic arch appearance and foramen ovale shunting aid detection, distinguishing true from false positives remains difficult, especially in late pregnancy.

Area of Science:

  • Cardiology
  • Fetal Medicine
  • Medical Imaging

Background:

  • Coarctation of the aorta is a critical congenital heart defect.
  • Accurate prenatal diagnosis is crucial for timely intervention.
  • Fetal echocardiography is the primary imaging modality for prenatal assessment.

Purpose of the Study:

  • To establish echocardiographic criteria for prenatal diagnosis of coarctation of the aorta.
  • To evaluate the effectiveness of specific echocardiographic measurements in identifying this condition.
  • To differentiate between true and false positive prenatal diagnoses.

Main Methods:

  • Retrospective analysis of fetal echocardiograms from a tertiary referral center.
  • Inclusion of fetuses with confirmed coarctation, suspected coarctation, and unproved diagnoses.
  • Measurement of ventricular dimensions, great artery diameters, atrioventricular valve orifice sizes, aortic arch appearance, and foramen ovale flow.

Main Results:

  • Ventricular and great artery measurements were insufficient for definitive diagnosis.
  • Aortic arch morphology, especially in horizontal projection, showed diagnostic potential but was not always conclusive.
  • A left-to-right shunt across the foramen ovale was more frequent in confirmed coarctation cases (58%) than in unproved cases (12%).

Conclusions:

  • Severe coarctation may present with relative left heart hypoplasia, diagnosable early.
  • Milder forms may have normal early fetal echocardiograms.
  • Distinguishing true from false positive diagnoses, particularly in late gestation, remains challenging due to overlapping features and normal fetal development variations.
Abstract

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