Disorders that occur as a result of a congenital anomaly where the heart developed inadequately in utero or cannot adapt to extrauterine life for some reason
If a parent has an aortic stenosis, atrial septal defect, ventricular septal defect, or pulmonic stenosis, the incidence of this occurring also in the child is about 10% to 15%
An opening is present in the septum between the two ventricles, causing blood to shunt from left to right across the septum, resulting in right ventricular hypertrophy and increased pressure in the pulmonary artery
If a VSD is left open, cardiac failure from the artery hypertension can result, and the heart can become infected (endocarditis) because of the recirculating blood flow
ASD closure is important because without it, a child is at risk for infectious endocarditis and eventual heart failure, and in girls it can cause emboli during pregnancy
If the ductus arteriosus does not close spontaneously, an infant may be prescribed IV indomethacin or ibuprofen, prostaglandin inhibitors, to encourage closure
If medical management fails to bring about closure of the ductus arteriosus, the disorder is closed by cardiac catheterization when the child is 6 months to 1 year of age, or exceptionally large defects are closed surgically by ductal ligation
Congenital anomalies that cause a vessel or valve to be narrower than usual, increasing pressure before the narrowing and decreasing pressure after the narrowing, prohibiting enough blood from reaching its intended site
Prevents blood from passing freely from the left ventricle of the heart into the aorta, leading to increased pressure and hypertrophy of the left ventricle
Narrowing of the lumen of the aorta due to a constricting band, more common in boys than girls and the leading cause of congestive heart failure in the first few months of life
Coarctation of the aorta can occur in two locations: preductal (between the subclavian artery and the ductus arteriosus) or postductal (distal to the ductus arteriosus)