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先天性高位气道梗阻综合征的成功胎儿干预。

Successful fetal intervention for congenital high airway obstruction syndrome.

作者信息

Paek Benita W, Callen Peter W, Kitterman Joseph, Feldstein Vickie A, Farrell Jody, Harrison Michael R, Albanese Craig T

机构信息

Department of Surgery, Division of Pediatric Surgery, University of California, San Francisco, Calif. 94143-0570, USA.

出版信息

Fetal Diagn Ther. 2002 Sep-Oct;17(5):272-6. doi: 10.1159/000063179.

Abstract

INTRODUCTION

Complete congenital high airway obstruction syndrome (CHAOS) usually leads to stillbirth or death within minutes of delivery. We describe the management and long-term follow-up of a baby with a prenatally diagnosed airway obstruction.

CASE

Because of progressive hydrops fetalis, massive ascites and everted diaphragms due to CHAOS in a fetus at 24 weeks of gestation, a fetal tracheostomy was performed. Persistent fetal bradycardia at the time of the fetal procedure led to delivery of the infant. Adequate oxygenation and ventilation were attained using relatively low oxygen concentrations and low ventilatory pressures. Plain radiographs demonstrated that the lungs were large and the ribs thin. The infant has a permanent tracheostomy, required continuous assisted ventilation for several months and assisted ventilation at night at home for 3 years. At 4 years of age, he has no speech, all feedings are by gastrostomy, and developmentally he is mildly to moderately delayed.

CONCLUSION

Laryngeal atresia produced over-distended lungs and hydrops. Precise prenatal imaging and fetal surgical strategies may allow the survival of affected fetuses.

摘要

引言

完全性先天性高位气道梗阻综合征(CHAOS)通常会导致死产或出生后几分钟内死亡。我们描述了一名产前诊断为气道梗阻的婴儿的治疗及长期随访情况。

病例

一名妊娠24周的胎儿因CHAOS导致进行性胎儿水肿、大量腹水和膈肌外翻,遂行胎儿气管造口术。胎儿手术时持续的胎儿心动过缓导致婴儿早产。使用相对低的氧浓度和低通气压力实现了充分的氧合和通气。X线平片显示肺部增大、肋骨变细。该婴儿有永久性气管造口,需要持续辅助通气数月,在家中夜间辅助通气3年。4岁时,他不会说话,所有喂养均通过胃造口进行,发育轻度至中度延迟。

结论

喉闭锁导致肺部过度扩张和水肿。精确的产前影像检查和胎儿手术策略可能使受影响的胎儿存活。

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