Abstract
The objective of this chapter is to tackle psychological issues pertaining to all the life phases of patients with congenital heart disease and their families – from the prenatal to the adult period. First and foremost, there will be a focus on communication to the families when it comes to the prenatal and neonatal period. It is particularly important for cardiologists to adjust their communication to the needs of the parents as they begin to cope with the cardiac condition. After that there will be an outline of the psychological functioning of patients with congenital heart disease from childhood to adulthood. In conclusion, some tips and considerations will be given to the medical professionals, in order for them to optimize the care they provide.
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References
Arya B, Glickstein JS, Levasseur SM, Williams IA (2013) Parents of children with congenital heart disease prefer more information than cardiologists provide. Congenit Heart Dis 8(1):78–85
Callus E, Quadri E, Ricci C, Passerini C, Tovo A, Pelissero G et al (2013) Update on psychological functioning in adults with congenital heart disease: a systematic review. Expert Rev Cardiovasc Ther 11(6):785–791
Latal B, Helfricht S, Fischer JE, Bauersfeld U, Landolt MA (2009) Psychological adjustment and quality of life in children and adolescents following open-heart surgery for congenital heart disease: a systematic review. BMC Pediatr 9:6
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© 2015 Springer-Verlag Italia
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Callus, E., Farè, C., Quadri, E. (2015). Psychological Aspects in Congenital Heart Disease: A Lifelong Perspective. In: Butera, G., Chessa, M., Eicken, A., Thomson, J. (eds) Cardiac Catheterization for Congenital Heart Disease. Springer, Milano. https://doi.org/10.1007/978-88-470-5681-7_10
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DOI: https://doi.org/10.1007/978-88-470-5681-7_10
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Publisher Name: Springer, Milano
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Online ISBN: 978-88-470-5681-7
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