Zusammenfassung
Der Begriff Kurzdarmsyndrom (KDS) beschreibt einen Zustand der Malabsorption, bei dem die verbleibende intestinale Funktion nicht zur Hydratation, der Homöostase der Elektrolyte und einem Gedeihen ausreicht. Das Syndrom tritt meist nach Resektion von großen Dünndarmanteilen auf, kann jedoch in seltenen Fällen auch angeboren sein (Wales et al. 2013). Das KDS ist ebenfalls definiert als die Abhängigkeit von einer parenteralen Ernährung (PN) infolge eines funktionellen oder anatomischen Verlusts von Darm (Andorsky et al. 2001).
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Lacher, M. (2018). Kurzdarmsyndrom bei Kindern. In: von Schweinitz, D., Ure, B. (eds) Kinderchirurgie. Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-53390-1_50-1
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