etralogy of Fallot is the most common form of cyanotic congenital heart disease and accounts for 3% to 5% of all congenital heart diseases. 1 The classic anatomic form of tetralogy of Fallot includes a subaortic ventricular septal defect, an aortic root that overrides the ventricular septal defect, infundibular pulmonary stenosis, and concentric right ventricular hypertrophy, with the last feature developing postnatally. More severe forms include right outflow obstruction such as an absent pulmonary valve and pulmonary atresia. Prenatal diagnosis in cases with severe obstruction provides the opportunity to administer early prostaglandin infusion after delivery to maintain ductal patency, thus avoiding life-threatening cyanosis in the early neonatal period. 2 However, the frequency of in utero diagnosis of tetralogy of Fallot has been reported to be only 32% to 47% and varies between different screening centers. [3][4][5][6][7] The contributing factors to the relatively low frequency of prenatal diagnosis are the frequently normal appearance of the 4-chamber view, poor visualization of the outflows tracts, and delay in the evolution of pulmonary atresia, which may only occur in the third trimester. [8][9][10] Anna Palatnik, MD, William A. Grobman, MD, MBA, Leeber S. Cohen, MD, Jeffrey S. Dungan, MD, Nina L. Gotteiner, MD Received September 17, 2015,
CASE SERIESPrenatal diagnosis of tetralogy of Fallot remains less frequent compared to other major congenital heart defects. In this study, we examined how often the 3-vessel and trachea view was abnormal in a large series of prenatally diagnosed cases of tetralogy of Fallot. In addition, we compared its sensitivity to that of the traditional outflow tract views for detection of tetralogy of Fallot. We found that both views were abnormal in all fetuses with tetralogy of Fallot, showing reversed aortic-to-pulmonary valve and aortic arch isthmus-to-ductus arteriosus ratios in the outflow tract and 3-vessel and trachea views, respectively. However, as a single measured marker, the enlarged aortic arch isthmus on the 3-vessel and trachea view appears to be the most sensitive for tetralogy of Fallot.