Coarctation of the aorta (CoA) is a relatively common defect that accounts for 5-8% of all congenital heart defects. Coarctation of the aorta may occur as an isolated defect or in association with various other lesions, most commonly bicuspid aortic valve and ventricular septal defect (VSD). It imposes significant afterload on the left ventricle (LV), which results in increased wall stress and compensatory ventricular hypertrophy.
Treatment in patients with Aortic Coarctation includes the use of diuretics and inotropic drugs. Prostaglandin E1 (0.05-0.15 mcg/kg/min) is infused intravenously to open the ductus arteriosus. Ventilatory assistance is provided to patients with markedly increased work of breathing. Infusion of inotropic drugs (dopamine, dobutamine, epinephrine) is useful when ventricular dysfunction is present, especially with hypotension. A Foley catheter is inserted to monitor renal perfusion and urine output.
Coarctation of the aorta is a common defect and occurs in 6-8% of patients with congenital heart disease. However, coarctation may be found more frequently in infants who present with symptoms prior to age one year. In Brazil, studies on the epidemiology with different cuts, express coefficients ranging from 5.494 to 7.17 per 1,000 births. For a group with low birth weight, the prevalence rate ranged from 10.7 to 40.7:1,000 births.