• Richard G Ohye, J William Gaynor, Nancy S Ghanayem, Caren S Goldberg, Peter C Laussen, Peter C Frommelt, Jane W Newburger, Gail D Pearson, Sarah Tabbutt, Gil Wernovsky, Lisa M Wruck, Andrew M Atz, Steve D Colan, James Jaggers, Brian W McCrindle, Ashwin Prakash, Michael D Puchalski, Lynn A Sleeper, Mario P Stylianou, Lynn Mahony, and Pediatric Heart Network Investigators.
• University of Michigan Medical School, Ann Arbor, Michigan, USA. ohye@umich.edu
• J. Thorac. Cardiovasc. Surg. 2008 Oct 1;136(4):968-75.

ObjectiveThe initial palliative procedure for patients born with hypoplastic left heart syndrome and related single right ventricle anomalies, the Norwood procedure, remains among the highest risk procedures in congenital heart surgery. The classic Norwood procedure provides pulmonary blood flow with a modified Blalock-Taussig shunt. Improved outcomes have been reported in a few small, nonrandomized studies of a modification of the Norwood procedure that uses a right ventricle-pulmonary artery shunt to provide pulmonary blood flow. Other nonrandomized studies have shown no differences between the two techniques.MethodsThe Pediatric Heart Network designed a randomized clinical trial to compare outcomes for subjects undergoing a Norwood procedure with either the right ventricle-pulmonary artery or modified Blalock-Taussig shunt. Infants with a diagnosis of single, morphologically right ventricle anomaly who are undergoing a Norwood procedure are eligible for inclusion in this study. The primary outcome is death or cardiac transplant 12 months after random assignment. Secondary outcomes include postoperative morbidity after Norwood and stage II palliation procedures, right ventricular function and pulmonary arterial growth at stage II palliation, and neurodevelopmental outcomes at 14 months old. Incidence of adverse events will also be compared between treatment groups.ConclusionThis study will make an important contribution to the care of patients with hypoplastic left heart syndrome and related forms of single, morphologically right ventricle. It also establishes a model with which other operative interventions for patients with congenital cardiovascular malformations can be evaluated in the future.

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