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Adults who survived repair of congenital oesophageal atresia and tracheo-oesophageal fistula.

机译:在先天性食管闭锁和气管食管瘘修复中幸存的成年人。

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摘要

One hundred and twenty five adults who were born before 1969 with oesophageal atresia or tracheo-oesophageal fistula or both and were managed at the Royal Children's Hospital, Melbourne, were reviewed. Most enjoyed a normal life. Though over half had difficulties in swallowing and symptoms of gastro-oesophageal reflux, the symptoms occurred only occasionally and were regarded as inconsequential by most. One third of the patients had wheeze and a quarter had at least one episode of bronchitis a year, but these interfered little with daily activities. Overall, these results are encouraging for young patients with oesophageal atresia and their families.
机译:回顾了在墨尔本皇家儿童医院接受治疗的1969年以前出生的125例食管闭锁或气管食管瘘或两者兼有的成年人。大多数人过着正常的生活。尽管超过一半的人有吞咽困难和胃食管反流的症状,但这种症状仅偶发,大多数人认为是无关紧要的。三分之一的患者患有气喘,四分之一的患者一年至少发作一次支气管炎,但这些对日常活动的影响很小。总体而言,这些结果对于年轻的食管闭锁患者及其家属而言是令人鼓舞的。

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