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The Long-Term Follow-Up from the Parents’ and Patient’s Perspective

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Esophageal and Gastric Disorders in Infancy and Childhood
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Abstract

Corrective surgery of esophageal atresia (EA) does not mean that a patient’s health is fully restored. Potential early or late complications may affect the private, social, and working life of patients and their families. Patient Support Organizations (PSOs) provide support to patients and their families by offering practical assistance. By making their own offers and proposing their own concepts, they contribute to the improvement of the patients’ medical care.

In Europe PSOs encourage the establishment of guidelines and standardized checklists for the lifelong follow-up of patients who underwent surgical EA repair. Based on multicenter data, the PSOs take part in the evaluation and optimization of guidelines and treatment concepts focusing on EA-related morbidity and their development from infant age to late adulthood.

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Trompelt, J. (2017). The Long-Term Follow-Up from the Parents’ and Patient’s Perspective. In: Till, H., Thomson, M., Foker, J., Holcomb III, G., Khan, K. (eds) Esophageal and Gastric Disorders in Infancy and Childhood. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-11202-7_57

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  • DOI: https://doi.org/10.1007/978-3-642-11202-7_57

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