Journal of the American Society of Echocardiography
Volume 22, Issue 11 , Pages 1296-1301, November 2009

Left Ventricle to Right Ventricle Size Discrepancy in the Fetus: The Presence of Critical Congenital Heart Disease Can Be Reliably Predicted

  • Michael D. Quartermain, MD

      Affiliations

    • Fetal Heart Program, The Cardiac Center at The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
    • Corresponding Author InformationReprint requests: Michael D. Quartermain, MD, The Children's Hospital of Philadelphia, 34th and Civic Center Boulevard, Division of Cardiology, Main Bldg, 8th Floor, Philadelphia, PA 19104
  • ,
  • Meryl S. Cohen, MD

      Affiliations

    • Fetal Heart Program, The Cardiac Center at The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
  • ,
  • Troy E. Dominguez, MD

      Affiliations

    • Cardiothoracic Unit, Great Ormond Street Hospital for Children, London, United Kingdom
  • ,
  • Zhiyun Tian, MD

      Affiliations

    • Fetal Heart Program, The Cardiac Center at The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
  • ,
  • Denise D. Donaghue, RN, MSN

      Affiliations

    • Fetal Heart Program, The Cardiac Center at The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
  • ,
  • Jack Rychik, MD

      Affiliations

    • Fetal Heart Program, The Cardiac Center at The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania

published online 08 October 2009.

Background

Prenatal ventricular size discrepancy with disproportionately smaller left ventricle than right ventricle (L-R/VD) can be a marker for important left-sided structural heart disease in the newborn.

Methods

We reviewed the echocardiograms of all fetuses evaluated at our center with L-R/VD from July 1, 2004 to January 1, 2008.

Results

Of the 35 fetuses, 20 (57%) had critical arch obstruction and underwent neonatal intervention (group 1); 15 (43%) did not require newborn intervention (group 2). Ratios comparing left with right heart structures were significantly lower in group 1 fetuses compared with group 2 fetuses. Aortic arch measurement ≤ 3 mm was the most sensitive, and abnormal direction of atrial level shunting was the most specific measure to predict the need for neonatal aortic arch intervention.

Conclusion

Ratios expressing the magnitude of L-R/VD, direction of flow at the atrial septum, and measurements of the aortic arch help identify fetuses that will require neonatal intervention.

Keywords: Aortic arch, Coarctation, Congenital heart disease, Echocardiogram, Fetal

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0894-7317(09)00759-7

doi:10.1016/j.echo.2009.08.008

Journal of the American Society of Echocardiography
Volume 22, Issue 11 , Pages 1296-1301, November 2009