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Ann Thorac Surg 2007;84:1633-1638. doi:10.1016/j.athoracsur.2007.06.061
© 2007 The Society of Thoracic Surgeons

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Sarah Tabbutt
J. William Gaynor
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Original Articles: Cardiovascular

Hypoplastic Left Heart Syndrome With Atrial Level Restriction in the Era of Prenatal Diagnosis

Jenifer A. Glatz, MDa, Sarah Tabbutt, MD, PhDa, J. William Gaynor, MDb, Jonathan J. Rome, MDa, Lisa Montenegro, MDc, Thomas L. Spray, MDb, Jack Rychik, MDa,*

a Department of Pediatrics, Children’s Hospital of Philadelphia and the University Hospital of Pennsylvania, Philadelphia, Pennsylvania
b Department of Cardiothoracic Surgery, Children’s Hospital of Philadelphia and the University Hospital of Pennsylvania, Philadelphia, Pennsylvania
c Department of Anesthesiology, Children’s Hospital of Philadelphia and the University Hospital of Pennsylvania, Philadelphia, Pennsylvania

Accepted for publication June 21, 2007.

* Address correspondence to Dr Rychik, Children’s Hospital of Philadelphia, Division of Cardiology, 34th and Civic Center Blvd, Philadelphia, PA 19104 (Email: rychik{at}email.chop.edu).

Background: Despite recent improvements in survival of patients with hypoplastic left heart syndrome, those with severe atrial level restriction continue to face higher rates of mortality. We sought to assess the impact of prenatal diagnosis and immediate intervention on the outcome of this high-risk population.

Methods: We performed a retrospective review of patients with hypoplastic left heart syndrome and restriction at the atrial level born between 1997 and 2006. Patients with an intact atrial septum or an interatrial communication less than 2 mm by color Doppler flow mapping on initial postnatal study, or evidence of obstruction to left atrial egress on fetal echocardiogram, were included. Patients were subdivided into two groups based on severity of obstruction.

Results: Thirty-eight patients met inclusion criteria; 16 had the most severe form of anatomic obstruction (group 1), and 22 had a lesser degree of obstruction (group 2). Thirty-day cumulative survival for all was 68%: 38% for group 1 and 94% for group 2 (p = 0.001). Twenty-six of the 38 patients (68%) were prenatally diagnosed. Prenatal diagnosis did not improve initial hospital survival or cumulative survival for either group. Eight patients had progression of atrial level restriction from the first fetal study to the first postnatal study. Seven patients prenatally diagnosed with severe restriction underwent planned cesarean section followed by immediate surgical or catheter-based intervention, with only 2 survivors (28%).

Conclusions: Hypoplastic left heart syndrome with an intact atrial septum is a highly lethal condition despite prenatal diagnosis and immediate intervention at birth. Fetal intervention should be considered for these high-risk fetuses.


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Invited commentary
James Lock and Audrey C. Marshall
Ann. Thorac. Surg. 2007 84: 1638-1639. [Extract] [Full Text] [PDF]



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J. Lock and A. C. Marshall
Invited commentary
Ann. Thorac. Surg., November 1, 2007; 84(5): 1638 - 1639.
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