Coarctation of the Aorta

Coarctation of the Aorta (CoA)

Coarctation of the aorta (CoA) is a congenital heart defect where the aorta is narrowed, restricting proper blood flow and increasing heart strain.

What is Coarctation of the Aorta?

Coarctation of the aorta (CoA) is a birth defect in which the aorta, the body's main artery, is abnormally narrowed (coarctated). This narrowing increases pressure before the narrowing point and decreases blood flow to the lower body. Over time, if untreated, this can cause serious complications such as high blood pressure, heart failure, or aortic rupture.

The severity of CoA can range from mild to severe. Some infants may experience symptoms soon after birth, while others may not be diagnosed until later in childhood or adulthood. The condition often occurs alongside other congenital heart defects, particularly bicuspid aortic valve disease.

Causes and Risk Factors

Coarctation of the aorta is a congenital condition, meaning it develops before birth. While the exact cause is not always known, several factors increase the likelihood of CoA:

Symptoms of Coarctation of the Aorta

The severity of symptoms depends on the degree of narrowing and whether other heart defects are present. Symptoms may appear in infancy or later in life.

Signs and Symptoms in Infants:

Signs and Symptoms in Older Children and Adults:

Diagnosis of Coarctation of the Aorta

Doctors use several tests to confirm a CoA diagnosis:

Treatment and Management

The treatment approach depends on the severity of the narrowing and whether symptoms are present.

Medical Management

Procedural Treatments

Long-Term Management and Follow-Up

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