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新生儿呼吸窘迫与气道急症:两例报告

Neonatal Respiratory Distress and Airway Emergency: Report of Two Cases.

作者信息

Bresciani Lorenzo, Grazioli Paola, Bosio Roberta, Chirico Gaetano, Zambelloni Cesare, Santoro Amerigo, Baronchelli Carla, Redaelli de Zinis Luca O

机构信息

Pediatric Otolaryngology Head Neck Surgery, Children Hospital "ASST Spedali Civili", 25123 Brescia, Italy.

Department of Neonatology and Neonatal Intensive Care Unit, Children Hospital "ASST Spedali Civili", 25123 Brescia, Italy.

出版信息

Children (Basel). 2021 Mar 25;8(4):255. doi: 10.3390/children8040255.

Abstract

We discuss two cases of congenital airway malformations seen in our neonatal intensive care unit (NICU). The aim is to report extremely rare events characterized by immediate respiratory distress after delivery and the impossibility to ventilate and intubate the airway. The first case is a male twin born at 34 weeks by emergency caesarean section. Immediately after delivery, the newborn was cyanotic and showed severe respiratory distress. Bag-valve-mask ventilation did not relieve the respiratory distress but allowed for temporary oxygenation during subsequent unsuccessful oral-tracheal intubation (OTI) attempts. Flexible laryngoscopy revealed complete subglottic obstruction. Postmortem analysis revealed a poly-malformative syndrome, unilateral multicystic renal dysplasia with a complete subglottic diaphragm, and a tracheo-esophageal fistula (TEF). The second case is a male patient that was vaginally born at 35 weeks. Antenatally, an ultrasound (US) arose suspicion for a VACTERL association (vertebral defects, anal atresia, TEF with esophageal atresia and radial or renal dysplasia, plus cardiovascular and limb defects) and a TEF, and thus, fetal magnetic resonance (MRI) was scheduled. Spontaneous labor started shortly thereafter, before imaging could be performed. Respiratory distress, cyanosis, and absence of an audible cry was observed immediately at delivery. Attempts at OTI were unsuccessful, whereas bag-valve-mask ventilation and esophageal intubation allowed for sufficient oxygenation. An emergency tracheostomy was attempted, although no trachea could be found on cervical exploration. Postmortem analysis revealed tracheal agenesis (TA), renal dysplasia, anal atresia, and a single umbilical artery. Clinicians need to be aware of congenital airway malformations and subsequent difficulties upon endotracheal intubation and must plan for multidisciplinary management of the airway at delivery, including emergency esophageal intubation and tracheostomy.

摘要

我们讨论了在我们新生儿重症监护病房(NICU)中见到的两例先天性气道畸形病例。目的是报告极为罕见的事件,其特征为出生后立即出现呼吸窘迫,且无法对气道进行通气和插管。第一例是一名34周时通过紧急剖宫产出生的男双胞胎。出生后立即出现青紫,并表现出严重的呼吸窘迫。球囊面罩通气未能缓解呼吸窘迫,但在随后经口气管插管(OTI)尝试失败期间实现了临时氧合。可弯曲喉镜检查显示声门下完全梗阻。尸检分析显示为多畸形综合征,单侧多囊性肾发育不良伴完全性声门下膈,以及气管食管瘘(TEF)。第二例是一名35周时经阴道出生的男性患者。产前,超声(US)怀疑存在VACTERL联合征(椎体缺陷、肛门闭锁、伴有食管闭锁的TEF以及桡骨或肾脏发育不良,加上心血管和肢体缺陷)和TEF,因此安排了胎儿磁共振成像(MRI)检查。此后不久,在进行成像检查之前自然分娩开始。分娩时立即观察到呼吸窘迫、青紫且无哭声。OTI尝试失败,而球囊面罩通气和食管插管实现了充分氧合。尽管在颈部探查时未找到气管,但仍尝试进行了紧急气管切开术。尸检分析显示气管缺如(TA)、肾脏发育不良、肛门闭锁和单脐动脉。临床医生需要意识到先天性气道畸形以及气管插管时随后出现的困难,并且必须在分娩时规划气道的多学科管理,包括紧急食管插管和气管切开术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4276/8064368/94299f2c2c9b/children-08-00255-g001.jpg

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