目的探讨先天性食道闭锁的转运和早期诊断及冶疗。
Objective To investigate the transport and early diagnosis and treatment of congenital esophageal atresia.
方法回顾性分析我院1999年9月至2003年11月收治的16例先天性食道闭锁患儿的外科资料。
Methods From september 1999 to November 2003,16 patients with congenital esophageal atresia were analyzed retrospectively.
结论：先天性食道闭锁修补术的合理麻醉处理应包括充分的术前准备、严格的呼吸循环管理及严密的监测。
Conclusions: The keys to anesthetic management for esophageal atresia repair are strict respiration-circulation management, rigorous monitoring, and sufficient preparing is also important.
方法1991～2 0 0 0年间对40例低体重出生儿进行手术，以消化道疾病占绝大多数（95 .0 % ）。 大多为胃壁修补术、食道闭锁根治术、肠切除肠吻合术等。
Methods From 1991 to 2000, 40 low birth weight newborns underwent surgical operation in which 38 had digestive tract diseases (95%) including esophageal atresia, gastrointestinal perforation.
方法1991～2 0 0 0年间对40例低体重出生儿进行手术，以消化道疾病占绝大多数（95 .0 % ）。 大多为胃壁修补术、食道闭锁根治术、肠切除肠吻合术等。
Methods From 1991 to 2000, 40 low birth weight newborns underwent surgical operation in which 38 had digestive tract diseases (95%) including esophageal atresia, gastrointestinal perforation.
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