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Respiratory Care of Infants and Children with Congenital Tracheo-Oesophageal Fistula and Oesophageal Atresia

机译:先天性气管食管瘘和食管闭锁的婴幼儿呼吸道护理

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摘要

Despite acute respiratory and chronic respiratory and gastro-intestinal complications, most infants and children with a history of oesophageal atresia / trachea-oesophageal fistula [OA/TOF] can expect to live a fairly normal life. Close multidisciplinary medical and surgical follow-up can identify important co-morbidities whose treatment can improve symptoms and optimize pulmonary and nutritional outcomes. This article will discuss the aetiology, classification, diagnosis and treatment of congenital TOF, with an emphasis on post-surgical respiratory management, recognition of early and late onset complications, and long-term clinical outcomes. (C) 2015 Elsevier Ltd. All rights reserved.
机译:尽管有急性呼吸道疾病和慢性呼吸道及胃肠道并发症,但大多数有食管闭锁/气管食管瘘[OA / TOF]病史的婴儿和儿童可以期望过上相当正常的生活。密切的多学科医学和外科手术随访可以确定重要的合并症,其合并症可以改善症状并优化肺和营养结果。本文将讨论先天性TOF的病因,分类,诊断和治疗,重点是术后呼吸管理,早期和晚期发作并发症的识别以及长期临床结果。 (C)2015 Elsevier Ltd.保留所有权利。

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