Abstract
The tetralogy of Fallot (TOF) is the most common form of cyanotic congenital heart disease.
Few are, today, the patients with TOF that reach the adulthood in natural history. Innovations in the diagnosis and management of TOF have led to dramatic improvements in early survival. As a result, the population of TOF repair survivors is growing rapidly. Surgical management of TOF leaves anatomic and functional abnormalities in the majority of patients. We will discuss in this chapter the different issues related to the most important problems (as chronic pulmonary valve insufficiency and obstruction of the right ventricular outflow tract, right ventricular outflow tract aneurism, pulmonary branch artery stenosis, dilated ascending aorta, aortic regurgitation, residual ventricular septal defect, arrhythmic problems) that we can face during the daily clinical practice, managing these patients.
We will conclude discussing some important aspects of the post-op management of the right ventricular function.
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Isgrò, G., Giamberti, A., Ranucci, M., Foresti, S., Chessa, M. (2023). The Adult with Tetralogy of Fallot. In: da Cruz, E.M., Ivy, D., Hraska, V., Jaggers, J. (eds) Pediatric and Congenital Cardiology, Cardiac Surgery and Intensive Care. Springer, London. https://doi.org/10.1007/978-1-4471-4999-6_185-2
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