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Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Medical management of the failing Fontan
N S Ghanayem1, S Berger, J S Tweddell
1Department of Pediatrics, Division of Critical Care, Children's Hospital of Wisconsin and Medical College of Wisconsin, 9000 West Wisconsin Avenue, MS 681, Milwaukee, WI 53226, USA. nghanayem@aol.com
Insights
The Fontan operation improves survival for single ventricle patients. Recognizing and managing Fontan failure is crucial for long-term health and preventing complications like heart failure and stroke.
Area of Science:
- Cardiology
- Pediatric Cardiac Surgery
- Congenital Heart Disease
Background:
- The Fontan operation separates systemic and pulmonary circulation in single ventricle patients.
- Surgical advancements and improved care have led to excellent operative survival.
- Increased Fontan survivors necessitate focus on long-term management and potential complications.
Purpose of the Study:
- To highlight the importance of recognizing and managing failing Fontan physiology.
- To emphasize the risks associated with long-term survival after the Fontan operation.
- To underscore the need for preserving single ventricle function and avoiding late complications.
Main Methods:
- Review of current literature on Fontan operation outcomes and complications.
- Analysis of pathophysiologic processes leading to Fontan failure.
- Discussion of strategies for long-term patient management.
Main Results:
- Excellent early survival rates are achieved with modern Fontan palliation.
- Late survivors face risks including ventricular dysfunction, arrhythmias, hypoxemia, and protein-losing enteropathy.
- Complications can include myocardial failure, thromboembolism, and stroke.
Conclusions:
- Long-term survival depends on preserving single ventricle function.
- Early recognition and treatment of Fontan failure are essential.
- Ongoing management is critical to mitigate late morbidities and ensure sustained patient health.
Abstract:
The Fontan operation accomplishes complete separation of systemic venous blood from pulmonary venous circulation in patients with single ventricle anatomy. Operative survival since the first description of the Fontan operation is excellent in the current era through modifications in surgical techniques, identification of patient-specific risk factors, and advances in postoperative care. Improved early outcomes have also resulted in a decline in late mortality for patients who have undergone staged palliation with the Fontan operation. As the number of late survivors from the Fontan operation increases, caregivers will be evermore faced with the challenge of recognizing and managing the patient with failing Fontan physiology. Even after excellent early results, patients with single ventricle lesions remain at risk of progressive ventricular dysfunction, dysrhythmias, progressive hypoxemia, elevated pulmonary vascular resistance, and protein-losing enteropathy, which can result in morbidities including but not limited to, myocardial failure, thromboembolism, and stroke. Consequently, continued long-term survival of patients who undergo the Fontan operation is dependent upon preservation of single ventricle function, avoidance of late complications, and, in the patient with a failing Fontan, recognition and treatment of the underlying pathophysiologic process that has resulted in Fontan failure.
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