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on June 28, 2004

Circulation. 2004
Published online before print June 28, 2004, doi: 10.1161/01.CIR.0000135471.17922.17
A more recent version of this article appeared on July 20, 2004
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Right arrow Catheter-based coronary and valvular interventions: other
Right arrow Pediatric and congenital heart disease, including cardiovascular surgery

Submitted on September 30, 2003
Revised on March 25, 2004
Accepted on March 26, 2004

Creation of an Atrial Septal Defect In Utero for Fetuses With Hypoplastic Left Heart Syndrome and Intact or Highly Restrictive Atrial Septum

Audrey C. Marshall MD*, Mary E. van der Velde MD, Wayne Tworetzky MD, Carlen A. Gomez MD, Louise Wilkins-Haug MD, PhD, Carol B. Benson MD, Russell W. Jennings MD, and James E. Lock MD

From the Departments of Cardiology, Children’s Hospital, and Pediatrics, Harvard Medical School, Boston, Mass (A.C.M., W.T., J.E.L.); Division of Pediatric Cardiology, C.S. Mott Children’s Hospital, Ann Arbor, Mich (M.E.v.d.V., C.A.G.); Departments of Obstetrics and Gynecology (L.W.-H.) and Radiology (C.B.B.), Brigham and Women’s Hospital and Harvard Medical School, Boston, Mass; and Department of Surgery, Children’s Hospital and Harvard Medical School, Boston, Mass (R.W.J.).

* To whom correspondence should be addressed. E-mail: Audrey.marshall{at}cardio.chboston.org.

Background--Infants born with hypoplastic left heart syndrome and an intact or highly restrictive atrial septum face a neonatal mortality of at least 48% despite early postnatal left atrial decompression and palliative surgery. Prenatal left atrial decompression has been suggested as a means of improving these outcomes. This study reports the feasibility of fetal catheterization to create an interatrial communication and describes technical considerations.

Methods and Results--Seven fetuses at 26 to 34 weeks’ gestation with hypoplastic left heart syndrome and intact or highly restrictive atrial septum underwent attempted prenatal intervention. Under ultrasound guidance, the atrial septum was approached with a needle introduced percutaneously from the maternal abdominal surface. In 6 of 7 fetuses, the atrial septum was successfully perforated, with balloon dilation of this iatrogenic defect resulting in a small but persistent interatrial communication. There were no maternal complications. One fetus died after the procedure. The remaining fetuses were liveborn at term, although 4 died as neonates.

Conclusions--Ultrasound-guided fetal atrial septoplasty consisting of septal puncture and balloon dilation is feasible and can be performed percutaneously to minimize maternal risk. Although we have not demonstrated any positive clinical impact to date, it is our hope that further technical evolution will ultimately enable prenatal left atrial decompression and improvement of outcomes in fetuses with hypoplastic left heart syndrome and intact atrial septum.


Key words: catheterization • heart defects, congenital • pregnancy




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