Sagy M, Silver P, Nimkoff L, Zahtz G, Amato J J, Bierman F Z
Division of Pediatric Critical Care, Schneider Children's Hospital, New Hyde Park, New York 11042.
Pediatr Emerg Care. 1994 Dec;10(6):351-8. doi: 10.1097/00006565-199412000-00014.
We describe seven patients who had intrathoracic airway obstruction resulting in severe respiratory distress. The patients were a four month old with bronchial cartilage hypoplasia presenting as congenital lobar emphysema; a one month old with segmental bronchomalacia; a one month old with tracheal bronchus; a two day old and a seven month old with aneurysmal distension of the pulmonary arteries secondary to tetralogy of Fallot, with absent pulmonary valve and atrioventricular canal with pulmonary poststenotic dilatation, respectively; a three year old with double aortic arch forming a vascular ring; and a three month old with tracheomalacia from tracheoesophageal fistula. The patients had various associated congenital defects, and all of them required one or more surgical procedures to repair the defects and relieve the airway obstruction. Five patients received endotracheal intubation with mechanical ventilation on their first admission, and three of them died postoperatively. The diagnostic workup to delineate the anatomic factors causing the obstruction, as well as to determine the therapeutic medical and surgical strategies to relieve it, are described. We conclude that the course of illness in most pediatric patients with intrathoracic airway obstruction is complex, is associated with high morbidity and mortality, and entails extensive multidisciplinary diagnostic and therapeutic efforts.
我们描述了7例因胸内气道阻塞导致严重呼吸窘迫的患者。这些患者包括:一名4个月大患有支气管软骨发育不全并表现为先天性大叶性肺气肿的婴儿;一名1个月大患有节段性支气管软化症的婴儿;一名1个月大患有气管支气管的婴儿;一名2日龄和一名7个月大分别因法洛四联症继发肺动脉瘤样扩张、肺动脉瓣缺如以及房室通道伴肺动脉狭窄后扩张的婴儿;一名3岁患有形成血管环的双主动脉弓的儿童;以及一名3个月大因气管食管瘘导致气管软化的婴儿。这些患者伴有各种相关的先天性缺陷,且均需要进行一次或多次外科手术来修复缺陷并解除气道阻塞。5例患者首次入院时接受了气管插管及机械通气,其中3例术后死亡。本文描述了用于明确导致阻塞的解剖学因素以及确定缓解阻塞的内科和外科治疗策略的诊断检查。我们得出结论,大多数患有胸内气道阻塞的儿科患者病程复杂,发病率和死亡率高,需要广泛的多学科诊断和治疗努力。