Congenital Heart Disease

2021-02-23 12:00 AM

Congenital heart disease is the most common cause of childhood heart disease in the United States;

CONGENITAL HEART DISEASE

Congenital heart disease is the most common cause of childhood heart disease in the United States; 90% of cases are idiopathic and 5% are associated with genetic disease (trisomies, cri du chat, Turner syndrome, etc.), viral infection (especially congenital rubella), or drugs and alcohol.

Coarctation of the aorta is a segmental narrowing of the aorta.

  • Preductal coarctation (infantile-type) is associated with Turner syndrome and causes severe narrowing of the aorta proximal to the ductus arteriosus. It is usually associated with a patent ductus arteriosus (PDA), which supplies blood to the aorta distal to the narrowing, and right ventricular hypertrophy (secondary to the need for the right ventricle to supply the aorta through the patent ductus arteriosus). It presents in infancy with congestive heart failure that is accompanied by weak pulses and cyanosis in the lower extremities; the prognosis is poor without surgical correction.
  •  Postductal coarctation(adult-type) causes stricture or narrowing of the aorta distal to the ductus arteriosus. It can present in a child or an adult with hypertension in the upper extremities, and hypotension and weak pulses in the lower extremities. Some collateral circulation may be supplied via the internal mammary and intercostal arteries; the effects of this collateral circulation may be visible on chest x-ray with notching of the ribs due to bone remodelling as a consequence of increased blood flow through the intercostal arteries.

Complications can include congestive heart failure (the heart is trying too hard), intracerebral haemorrhage (the blood pressure in the carotid arteries is too high), and dissecting aortic aneurysm (the blood pressure in the aortic route is too high).

Tetralogy of Fallot is the most common cause of congenital cyanotic heart disease. The classic tetrad includes right ventricular outflow obstruction/stenosis; right ventricular hypertrophy; ventricular septal defect; and an overriding aorta. Clinical findings include cyanosis, shortness of breath, digital clubbing, and polycythemia. Progressive pulmonary outflow stenosis and cyanosis develop over time; treatment is surgical correction.

Truncus arteriosus is a failure to develop a dividing septum between the aorta and pulmonary artery, resulting in a common trunk. Blood flows from the pulmonary trunk to the aorta. Truncus arteriosus causes early cyanosis and congestive heart failure, with a poor prognosis without surgery.

Tricuspid atresia refers to the absence of communication between the right atrium and ventricle due to developmental failure to form the tricuspid valve. Associated defects include right ventricular hypoplasia and an ASD. The prognosis is poor without surgery.

Ventricular septal defect (VSD), which consists of direct communication between the ventricular chambers, is the second most common congenital heart defect (the most common is a bicuspid aortic valve).

  • small ventricular septal defect may be asymptomatic and close spontaneously, or it may produce a jet stream that damages the endocardium and increases the risk of infective endocarditis.
  •  A large ventricular septal defect may cause the Eisenmenger complex, which is characterized by secondary pulmonary hypertension, right ventricular hyper-trophy, reversal of the shunt, and late cyanosis.
  •  In both types, a systolic murmur can be heard on auscultation. Ventricular septal defects are commonly associated with other heart defects. Large ven-tricular septal defects can be surgically corrected.

Atrial septal defect (ASD) is direct communication between the atrial chambers.

The most common type is an ostium secundum defect. Complications include Eisenmenger syndrome and paradoxical emboli.

Patent ductus arteriosus (PDA) is direct communication between the aorta andpulmonary artery due to the continued patency of the ductus arteriosus after birth. It is associated with prematurity and congenital rubella infections. Clinical findings include machinery murmur, late cyanosis, and congestive heart failure. Eisenmenger syndrome may develop as a complication.