Aortic coarctation (patient information)
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Aortic coarctation |
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Aortic coarctation On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S. [2]; Jinhui Wu, M.D.; Assistant Editor(s)-In-Chief: Kristin Feeney, B.S. [3]
Overview
Aortic coarctation is a congenital heart disease with a narrowing part of the aorta. This condition leads the heart must pump harder to force blood through the narrow part of the narrowing aorta. The cause is not clear. Usual signs and symptoms of aortic coarctation include dizziness or fainting, shortness of breath, headache, chest pain and hypertension. Tests such as echocardiography and chest x-ray can show the enlarged left ventricle in patients with aortic coarctation. Treatments include medicines used to control hypertension, balloon angioplasty and stenting, and surgery. The prognosis of aortic coarction depends on the effect of balloon angioplasty and stenting or surgery.
What are symptoms of Aortic coarctation?
The signs and symptoms of coarctation of the aorta depend on how much blood can flow through the artery. Children with serious aortic narrowing tend to show signs and symptoms earlier in life, while mild cases may not be diagnosed until adulthood. Usual symptoms include:
Other health problems may also cause these symptoms. Only a doctor can tell for sure. A person with any of these symptoms should tell the doctor so that the problems can be diagnosed and treated as early as possible.
What are causes Aortic coarctation?
The aorta carries blood from the heart to the vessels that supply the body with blood and nutrients. If part of the aorta is narrowed, it is hard for blood to pass through the artery. Aortic coarctation is more common in persons with certain genetic disorders, such as Turner syndrome. However, it can also be due to birth defects of the aortic valves. Aortic coarctation is one of the more common heart conditions that are present at birth (congenital heart conditions). It is usually diagnosed in children or adults under age 40.
Coarctation of the aorta may be seen with other congenital heart defects, such as:
- Bicuspid aortic valve
- Defects in which only one ventricle is present
- Ventricular septal defect
Who is at highest risk?
Like many congenital heart disease, the cause of aortic coarctation is not clear. Clinical studies suggest that genetic and environmental factors both play an important role during pregnancy. These include:
- Genetic disorders such as Turner syndrome
- Viral infections during pregnancy
Diagnosis
- Echocardiography Echocardiography is the most commonly used imaging technique for the diagnosis of aortic coarctation. It can assess atrium and ventricle morphology and characteristic anatomic relations, and detect the location and severity of the aortic coarctation and can show other heart defects, such as a bicuspid aortic valve.
- Electrocardiogram (ECG) and Holter monitoring Electrocardiogram and Holter monitoring can tell electric activities of the heart for cardiovascular diseases. They can supply informations about heart rhythm and indirectly, heart size. Patients with aortic coarctation may show ventricular hypertrophy and heart rhythm irregularity sign.
- Chest x-ray An x-ray image of chest allows the doctor to check the size and shape of the heart to determine whether the heart is enlarged. And it also helps the doctor check the condition of your lungs. Patients with aortic coarctation may show an enlarged heart or a narrowing in the aorta at the site of the coarctation.
- Cardiac catheterization In a catheter room, the doctor threads a thin tube through a blood vessel in yourthe patient's arm or groin to an artery in the heart and injects dye to see the heart and the arteries on an x-ray. It can supply detailed information about the severity of the aortic coarctation.
- Cardiac MRI and CT Cardiac MRI and CT can create pictures of the ventricles, atrium, valves and major blood vessels. It can help doctors analyse the structure and function of the heart and decide the treatment protocols for the patient. Patient with aortic coarctation may reveal the location of the coarctation of the aorta and determine whether it affects other blood vessels in the child's body.
Treatment options
Patients with aortic coarctation have many treatment options. The selection depends on the severity of aortic coarctation, symptoms and whether the child occurs the complications or not. The options are medicines, balloon angioplasty and stenting, and surgery. The goal of the treatment is to open the aorta to prevent complications. Before treatment starts, talk to your child's doctor about treatment options and your family's preferences on treatment decisions.
- Medicines Some anti-hypertension medicines can be used to control blood pressure before or after surgery.
- Balloon angioplasty and stenting In a catheter room, the doctor threads a thin tube through a blood vessel in your baby's arm or groin to an artery in the heart. Then, an uninflated balloon is placed through the opening of the narrowed aorta and a stent is inserted to keep the narrowed part of the aorta open permanently.
- Surgery Surgical treatment of aortic coarctation may be performed to repair aortic coarctation. During the surgery, the anesthetist gives medicine to make the child sleepy and comfortable. Then the surgeons make a small cut between the ribs to reach the aorta and repair it. The methods for repairing include resection with end-to-end anastomosis, patch aortoplasty, left subclavian flap angioplasty and bypass graft repair.
Diseases with similar symptoms
Where to find medical care for aortic coarctation?
Directions to Hospitals Treating Aortic coarctation
What to expect (Outlook/Prognosis)?
The prognosis of aortic coarctation depends on whether balloon angioplasty and stenting or the surgery has been done or not.
Prevention
Although the cause is unknown, the following measures may be helpful to decrease the risk of having a baby with aortic coarctation.
- Screening test and regular check for people with genetic disorders, especially Turner syndrome.
- Pregnant woman need to avoiding viral infection during pregnancy.