Congenital Heart Disease
The Structural Heart Disease Program at the Heart & Vascular Institute-Texas Medical Center is staffed by specialists and subspecialists from the Division of Cardiovascular Medicine at The University of Texas Medical School at Houston, as well as by physicians in private practice. The team includes noninvasive cardiologists, interventional cardiologists and cardiovascular imaging specialists.
Research focused on novel percutaneous and endovascular therapies for the treatment of structural heart disease has opened the door to new minimally invasive treatments for a variety of non-coronary artery diseases. The benefits for patients are significant: less bleeding and need for blood transfusion, a shorter hospitalization and faster recovery.
For individuals who are diagnosed with congenital heart disease as an adult, our affiliated physicians provide comprehensive care for all conditions, including:
- Atrial septal defects
- Ventricular septal defects
- Patent foramen ovale (PFO)
- Pulmonary arteriovenous fistulas
- Patent ductus arteriosis
For concerns related to congenital heart disease in children, physicians affiliated with the Children’s Heart Institute at Children’s Memorial Hermann Hospital provide care for neonatal and pediatric patients.
Clinical research at Memorial Hermann-Texas Medical Center and the UT Medical School has led to the development of innovative approaches to the treatment of structural heart disease. Clinical research team members serve as principal investigators in local, national and international research trials, and publish the results of their research in major subspecialty journals and general medical journals such as the American Journal of Cardiology, Clinical Research, Circulation, Circulation Interventions, Journal of the American College of Cardiology, Journal of the American College of Cardiology-Interventions, Journal of Nuclear Medicine and Catheterization and Cardiac Interventions, among others.
To obtain a referral to a cardiologist affiliated with Memorial Hermann Heart & Vascular Institute-Texas Medical Center, call 713.222.CARE (2273).
An atrial septal defect (ASD) (link to) is a hole in the part of the septum that separates the left and right atria, or upper chambers of the heart. A hole in the septum between the heart’s two lower chambers, or ventricles, is called a ventricular septal defect (VSD) (link to).
Atrial septal defects and ventricular septal defects allow blood to pass from the left side of the heart to the right side. In the normal heart, with each heartbeat, the right side of the heart receives oxygen-poor blood from the body and pumps it into the lungs. The left side of the heart receives oxygen-rich blood from the lungs and circulates it through the body. ASDs and VSDs allow the escape of some oxygen-rich blood into the lungs instead of pumping it through the body.
Many infants born with ASDs have no signs or symptoms. If symptoms occur, shortness of breath and irregular heart rhythms are the most common. Medium to large unrepaired ASDs may cause arrhythmias, stroke or pulmonary hypertension.
Moderate to large VSDs may lead to heart failure, arrhythmias or failure to grow, especially in infancy.
A patent foramen ovale (PFO) is a small opening between the upper chambers of the heart that allows blood to bypass the lungs. Normally, a PFO closes shortly after birth but estimates indicate that in 1 out of 4 people, the opening never closes. Researchers suspect that PFOs may contribute to cryptogenic strokes, which are strokes with an unknown cause.
The cause of PFOs is unknown, and there are no known risk factors. Occasionally, PFOs and ASDs are associated with shunting of blood from the right atrium to the left atrium. When this occurs, the oxygen content of the arterial blood can drop, causing severe shortness of breath. In addition, small blood clots (or in the case of recreational or commercial divers, air bubbles) in the blood that shunts into the left atrium may result in stroke or heart attack. This right-to-left shunting in patients with PFOs and ASDs has also been associated with migraine headaches in some studies.
A pulmonary arteriovenous fistula is an abnormal connection, or fistula, that develops between an artery and vein in the lungs. As a result, blood passes through the lungs without receiving enough oxygen.
Pulmonary arteriovenous fistulas are usually the result of a genetic disease that causes the blood vessels of the lung to develop abnormally. Fistulas also can be a complication of liver disease.
These fistulas can result in the same symptoms described above in patients with PFOs and ASDs with right-to-left shunting.
In patent ductus arteriosis, abnormal blood flow occurs between two of the major arteries connected to the heart. Before birth, the aorta and the pulmonary artery are connected by a blood vessel called the ductus arteriosus, an essential part of fetal blood circulation.
While the vessel normally closes after birth, in some babies it remains open, allowing oxygen-rich blood from the aorta to mix with oxygen-poor blood from the pulmonary artery. The result is strain on the heart and increased blood pressure in the lung arteries.