Patent Foramen Ovale (PFO) Closure

A patent foramen ovale (PFO) closure is a procedure to close a small hole in the heart that exists during fetal development to promote blood flow and, in the majority of cases, either closes on its own during infancy or remains open but never causes problems. A small flap-like opening, the foramen ovale is located in the wall between the two upper chambers of the heart. In about one out of four people, the hole does not close on its own, but fewer than 1 percent of people ever need to have a PFO closed.

Closure may be recommended if the PFO is suspected to be causing otherwise unexplained strokes, transient ischemic attacks (TIAs, or “mini strokes”), or embolisms (bloodstream blockages). Closure involves a small incision usually made in the inner thigh area, through which a catheter holding a closure device is inserted into a large vein and slowly guided into the heart. Once the catheter reaches the PFO, the device is released and allowed to expand into the intended shape necessary to seal the hole. The catheter is then removed, but the closure device remains as a permanent implant. The procedure typically is followed by a chest X-ray and/or an echocardiogram to confirm that the device is properly positioned.

Why UAB

UAB Medicine operates a Marfan Syndrome and Related Disorders Clinic, which is a multi-specialty clinic that includes physicians from the UAB Department of Pediatric Cardiology and the UAB Department of Genetics. Services offered include physical exams, echocardiogram/EKG, and genetic testing for diseases and conditions of the aorta, when needed. The clinic’s genetic counselor works with patients to help them better understand their condition and evaluate their risk for medical issues based on genetic testing results.

Because Marfan syndrome can affect the heart, patient care also may be provided by the UAB Congenital Heart Disease Program. The program offers the most advanced care for congenital (present at birth) heart disease, which often requires lifetime monitoring and care. Our multi-specialty team of pediatric and adult cardiologists, cardiovascular surgeons, cardiovascular anesthesiologists, and maternal-fetal medicine specialists have unique expertise in treating patients before birth and into adulthood.

UAB Medicine’s modern ultrasound equipment allows many heart defects to be diagnosed before a child is born. Screening exams performed at 18-20 weeks are recommended for expecting mothers or fathers known to have congenital heart disease. If a defect is discovered, our experts provide prenatal treatment and develop a plan for delivery and treatment after birth.

Thanks to advances in pediatric congenital care, the life expectancy for most patients now reaches far into adulthood. However, more than half of the people with congenital heart problems stop seeing a cardiologist once they turn 18. UAB’s Alabama Adult Congenital Heart Disease Program is designed to prevent that gap in care. As the only adult congenital heart disease program in the state and one of only a few in the country, our expertise greatly increases the chances that symptoms will be identified early. This helps ensure that less serious problems are addressed before they develop into larger, more life-threatening issues such as heart failure, arrhythmia, residual congenital heart defects, endocarditis, and stroke.

VIDEOS

Dr. Marc Cribbs appeared on Fox 6 TV's "Business Break" to discuss Adult Congenital Heart Disease.

More than 20,000 adults enter the Adult Congenital Heart Disease population every year, but 60% are lost to follow-up care.

Individuals born with congenital heart disease are now thriving into adulthood, but need lifelong follow-up care from sub-specialty experts.

CARE PROVIDERS

Marc G. Cribbs, MD

Walter H. Johnson Jr., MD

Related Conditions

This procedure may be used to treat or diagnose several different conditions. We have listed some of these conditions below for your convenience. Please note that this is not a comprehensive list and may vary depending on your specific diagnosis.