Titlebook: Oesophageal Atresia; S. W. Beasley (Consultant Paediatric Surgeon),N. A Book 1991 Springer Science+Business Media Dordrecht 1991 anatomy.c

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Oesophageal replacement1986): in these, oesophageal replacement is needed. Although the size of this group has diminished considerably in recent years the surgeon who accepts responsibility for the care of the baby with oesophageal atresia must still be familiar with at least one of the techniques available.

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Diagnosise the type of anomaly and the presence of other major anomalies must be determined. Associated congenital anomalies are found in approximately 50% of babies with oesophageal atresia and their recognition is important in deciding treatment priorities (Chapter 14).

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PathophysiologyFollowing repair of oesophageal atresia, function of the oesophagus rarely attains complete normality. The suboptimal function is in part because of inherent abnormalities of the oesophagus, its sphincters and its motility, and in part results from the surgery required to correct the atresia.

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Transport of the neonate with oesophageal atresiaThe over-riding principle of transport of the newborn is stabilization before transport, followed by supervision of transport by specialist nursing and medical personnel with appropriate equipment.

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