Diagnosis of Congenital Heart Disease
Congenital heart disease is often first identified before birth through a fetal echocardiogram, an ultrasound examination that creates detailed images of the developing heart's structure and blood flow. After birth, a physical examination may reveal a heart murmur or abnormal breathing pattern that prompts further testing. Diagnostic tools used to confirm and characterize a heart defect include echocardiography, which remains the primary imaging method for evaluating heart structure and function in infants and children, along with electrocardiography to assess heart rhythm and, in more complex cases, cardiac MRI or catheterization to obtain a more detailed view of blood flow and pressure within the heart and vessels. Pulse oximetry screening, a simple test measuring blood oxygen levels, is also used routinely in newborns to help detect critical congenital heart disease that might not yet be causing visible symptoms.