Occurrence of Tension Pneumothorax following Fogarty Embolectomy Catheter use for Lung Isolation in a Neonate with Congenital Pulmonary Airway Malformation

J. Budzinski
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Abstract

A pneumothorax can arise in a variety of clinical settings in the operating room, from bleb rupture to iatrogenic injury. Should it expand in size and cause increase in intrapleural pressures with resultant diminished venous return, it becomes referred to as a tension pneumothorax. We report a case of a premature infant presenting for repair of congenital pulmonary airway malformation who suffered an iatrogenic tension pneumothorax during lung isolation with fogarty embolectomy catheter used for single lung ventilation in a neonate. via c-section was noticed to have respiratory difficulty shortly after birth. Radiologic investigations revealed a right-sided chest mass with slight mediastinal shift (Figure 1). A diagnosis of CPAM was made, and the child was scheduled for right upper lobectomy. He was otherwise healthy with no abnormal laboratory or clinical findings. The case was discussed with the surgical team, and it was decided to proceed with lung isolation and single-lung ventilation (SLV). Atropine was administered intravenously, and anesthesia was induced with propofol and rocuronium. Mask ventilation was instituted using minimal pressures with 2% sevoflurane and 100% oxygen. Direct laryngoscopy (DL) was performed and a 4 Fr Fogarty embolectomy catheter (FC) easily inserted until resistance was met. An initial attempt with Case RepoRt
福格蒂栓塞导管肺隔离术治疗新生儿先天性肺气道畸形后张力性气胸的发生
在手术室的各种临床环境中,从水泡破裂到医源性损伤,都可能发生肺气肿。如果它的大小扩大并导致胸膜内压力增加,从而导致静脉回流减少,它就被称为张力性肺气肿。我们报告了一例早产儿,该早产儿在使用fogarty栓子切除导管进行新生儿单肺通气的肺隔离期间,出现医源性张力性肺气肿,需要修复先天性肺气道畸形。通过剖腹产被发现在出生后不久出现呼吸困难。放射学检查显示右侧胸部肿块伴有轻微纵隔移位(图1)。诊断为CPAM,并安排孩子进行右上叶切除术。他在其他方面都很健康,没有任何异常的实验室或临床发现。与外科团队讨论了该病例,并决定继续进行肺部隔离和单肺通气(SLV)。阿托品静脉注射,丙泊酚和罗库诱导麻醉。使用2%七氟醚和100%氧气的最小压力进行面罩通气。进行直接喉镜检查(DL),并轻松插入4 Fr Fogarty栓子切除导管(FC),直到遇到阻力。案例报告的初步尝试
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