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Functionally Single-Ventricle Complications After Fontan Palliation-A Narrative Review
Małgorzata Kowalczyk1, Mirosław Kowalski1
1Department of Adult Congenital Heart Disease, National Institute of Cardiology in Warsaw, 04-628 Warsaw, Poland.
Insights
Functionally single-ventricle (FSV) defects require Fontan palliation, leading to long-term complications like organ dysfunction and psychosocial challenges. Comprehensive, multidisciplinary care is essential for managing these complex pediatric heart conditions.
Area of Science:
- Cardiology
- Pediatric Congenital Heart Disease
Background:
- Functionally single-ventricle (FSV) defects are complex congenital heart anomalies necessitating Fontan palliation.
- Fontan circulation, while improving survival, presents unique physiological challenges predisposing patients to long-term complications.
Purpose of the Study:
- To review the spectrum of cardiovascular and systemic complications associated with Fontan physiology.
- To highlight the impact of these complications on patients' quality of life and the need for comprehensive management.
Main Methods:
- Literature review of studies on Fontan palliation outcomes.
- Analysis of cardiovascular, systemic, and psychosocial complications in FSV patients.
Main Results:
- Key cardiovascular issues include ventricular dysfunction, valve regurgitation, arrhythmias, and thromboembolic events.
- Systemic complications comprise Fontan-associated liver disease (FALD), protein-losing enteropathy (PLE), plastic bronchitis (PB), renal, endocrine, and psychosocial burdens.
- These complications lead to frequent hospitalizations and impaired life opportunities.
Conclusions:
- Fontan physiology poses significant long-term risks requiring vigilant monitoring and management.
- A multidisciplinary approach is crucial to address the complex interplay of hemodynamic, organ-specific, and psychosocial factors in Fontan patients.
Abstract:
Functionally single-ventricle (FSV) defects are complex congenital heart anomalies that require Fontan palliation, a surgical procedure redirecting systemic venous blood directly to the pulmonary arteries, bypassing the heart. Despite improvements in surgical techniques and perioperative care leading to enhanced survival rates, patients remain vulnerable to significant long-term complications, due to the unique Fontan circulation physiology. This circulation relies on low pulmonary vascular resistance and preserved single-ventricle function but predisposes patients to venous congestion and reduced cardiac output, resulting in multi-organ dysfunction. Key cardiovascular complications include systolic and diastolic dysfunction of the single ventricle, atrioventricular valve regurgitation, arrhythmias, pulmonary vascular disease, and thromboembolic events. Systemic complications encompass Fontan-associated liver disease (FALD), protein-losing enteropathy (PLE), plastic bronchitis (PB), renal impairment, and endocrine and psychosocial burdens. All the problems induce frequent hospitalizations, psychological challenges, and impaired educational and employment opportunities. Comprehensive management requires multidisciplinary approaches addressing the complex interplay of hemodynamic, organ-specific problems, and psychosocial factors inherent to Fontan physiology.
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