Pediatr. praxi. 2011;12(6):411-413

Long-term morbidity in patients operated for esophageal atresia

MUDr.Jana Kalousová, MUDr.Jitka Stýblová, MUDr.Petra Kuklová, MUDr.Blanka Rousková
Klinika dětské chirurgie 2. LF UK a FN Motol, Praha
V ČR se ročně narodí 20&ndash,40 dětí s atrézií jícnu a/nebo tracheoezofageální píštělí. Na pracovišti autorů bylo během 17 let operováno 209

Between 20 and 40 infants with esophageal atresia are born in Czech Republic annually. During 17 years 209 infants with this diagnosis

were operated on in authors’ department. Mortality is relatively low (10 %) but chronic morbidity remains high especially in infants with

long-gap atresia. There are problems that persist lifelong in some patients. They include swallowing problems, failure to thrive, anastomotic

strictures, gastroesophageal reflux, respiratory problems, symptoms of tracheomalacie and psychosocial problems. Symptoms,

diagnosis and treatment of the most common delayed problems after operation of esophageal atresia are summarized.

Keywords: esophageal atresia, failure to thrive, swallowing problems, tracheomalacia, gastroesophageal reflux, esophagogastroplasty

Published: December 10, 2011  Show citation

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Kalousová J, Stýblová J, Kuklová P, Rousková B. Long-term morbidity in patients operated for esophageal atresia. Pediatr. praxi. 2011;12(6):411-413.
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