EUPSA/ERNICA · Care and Nutrition in Esophageal Atresia: An ERNICA animation for parents and families
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Video2 min·Published Nov 2023Older

Care and Nutrition in Esophageal Atresia: An ERNICA animation for parents and families

Chapter 1 of 1 · Patient & Family Education

EA care overview

Care and Nutrition Management in Esophageal Atresia

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What the experts said0 expert statements · 16 host summaries
Esophageal atresia is a rare birth defect where a part of the esophagus, the tube connecting the mouth to the stomach, is missing.
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All babies born with esophageal atresia should be treated at a specialist center with appropriate expertise and a dedicated multidisciplinary team.
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Because saliva, secretions and food cannot flow into the stomach, babies with esophageal atresia are at risk of aspiration, which is fluid entering the lungs.
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A replogle tube is placed through the mouth or nose into the esophagus to suck out all fluids, preventing leakage into the airway and thus preventing aspiration.
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The replogle tube enables giving the baby pleasant oral experiences and developing swallowing skills.
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With the replogle tube in place, parents may be able to give the baby a small taste of breast milk before esophageal repair using a pacifier or dummy.
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In rare circumstances when the baby needs a delayed repair, sham feeding may be helpful.
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In sham feeding, a baby's feed is provided orally but sucked out by the replogle tube, while the baby receives food directly into the stomach through a gastrostomy tube.
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Sham feeding can help the baby associate oral feeding with milk entering the stomach.
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A lactation consultant or support worker will support parents to bond with the baby, discuss feeding options and support with breastfeeding.
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Peer support can be accessed through patient and family support groups.
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A specialized swallowing therapist can assess the baby's swallowing and feeding, and if necessary, offer ongoing specific therapy and advice.
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A nutrition therapist will ensure that the baby meets all nutritional requirements to support optimal growth.
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For the first year after surgery, an outpatient review including a nutritional assessment is recommended to take place every 3 months.
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From the first year onward, nutritional assessments are recommended to occur every 2 years until transition to adult care.
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Lifelong follow up is now recommended for those born with esophageal atresia.
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