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1例新生儿先天性食道闭锁一期成形术的护理 被引量:3

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摘要 先天性食管闭锁和气管食管瘘(Congenital esphageal atresia and tracheoesophageal Pistcola)简称先天性食管闭锁,该病是新生儿期消化道一种严重消化道发育畸形,是胚胎发育3~6周发育障碍所致[1]。其临床表现为新生儿出生数小时即有发作性咳嗽、气急和暂时性紫绀。唾液过多,带泡沫的唾液从口腔鼻孔不断溢出。
出处 《当代护士(下旬刊)》 2009年第6期88-89,共2页 Modern Nurse
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  • 2Tercan E,Sungun MB,BoyaciA,et al.One-lung ventilation of a preterm newborn during esophageal atresia and tracheoesophageal fistula repair[J].Acta Anaesthesiol Scand,2002,46:332-333.
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  • 7朱军,周光萱,孙荣国,邓鸿云.先天性食管闭锁围产期死亡的危险因素分析[J].中华小儿外科杂志,1997,18(6):325-327. 被引量:17
  • 8李文涛,何晓明,孙丽娟,刘晶.间断雾化吸入预防呼吸机相关性肺炎的研究[J].实用护理杂志,2002,18(1):3-4. 被引量:47

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