Pathway Background and Objectives
The diagnosis of Tetralogy of Fallot carries a wide range of treatment possibilities based on the detailed cardiac anatomy. Neonates that are ductal dependent for adequate pulmonary blood flow can be at high risk for severe hypoxemia after delivery if not immediately recognized. Babies that are not ductal dependent may be discharged home if they have normal oxygen saturations, and elective surgery is planned at several months of age. Because the ductus arteriosus is open in utero and oxygen saturations cannot be predicted, determination of ductal dependency prenatally can be challenging. Secondary signs on a fetal echocardiogram can be helpful in predicting ductal dependency, such as flow across the pulmonary valve, size of the pulmonary arteries, and direction of flow across the ductus arteriosus. It is not, however, until after a baby is born that ductal dependency can be accurately determined. Based on the prenatal signs, we can estimate the degree of risk in order to guide our postnatal management and assessment.
The objectives of this clinical pathway are to:
- Ensure maximal safety for babies with potentially ductal dependent Tetralogy of Fallot
- Optimize the use of echocardiogram and available resources
- Decrease ambiguity and variability in evaluation and treatment of newborns with prenatally diagnosed Tetralogy of Fallot in the Neonatal Intensive Care Unit or Well Baby Nursery
- Minimize unnecessary separation of newborn babies from their mothers