Chen Jiaxiang, Shi Xiaoli, Tu Youbing, Chen Yuanzhen, Wang Xueqing, Shen Jing, Xu Liang, Meng Ligang
Department of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, China.
Front Pediatr. 2025 Jan 29;13:1496553. doi: 10.3389/fped.2025.1496553. eCollection 2025.
Pulmonary alveolar proteinosis (PAP) is a rare disease in infancy characterized by the accumulation of lipoprotein material within the alveoli, leading to impaired gas exchange, ventilation-perfusion mismatch, and, in severe cases, respiratory failure that may result in death. Treatment options include medical therapy and whole lung lavage (WLL), typically requiring lung isolation techniques or extracorporeal membrane oxygenation. Previous studies have reported the application of several lung isolation techniques in pediatric WLL. However, the use of a bronchial blocker (BB) in infant WLL has not been previously reported.
This study reports the anesthesia management of a 12-month-old infant diagnosed with secondary PAP, complicated by severe pneumonia and patent ductus arteriosus. The child presented with respiratory failure requiring WLL. The anesthesia method employed was intravenous general anesthesia, and airway management involved using a BB placed outside the endotracheal tube to facilitate one-lung ventilation (OLV). The procedure successfully maintained blood oxygen levels above 90%, and the WLL was completed without any anesthetic complications.
This case demonstrates that using endotracheal intubation combined with extraluminal placement of a BB for lung isolation is a viable and effective approach for performing WLL in infants.
肺泡蛋白沉积症(PAP)是一种罕见的婴儿疾病,其特征是肺泡内脂蛋白物质积聚,导致气体交换受损、通气-灌注不匹配,严重时可导致呼吸衰竭甚至死亡。治疗选择包括药物治疗和全肺灌洗(WLL),通常需要肺隔离技术或体外膜肺氧合。先前的研究报道了几种肺隔离技术在儿科WLL中的应用。然而,支气管封堵器(BB)在婴儿WLL中的应用此前尚未见报道。
本研究报告了一名12个月大婴儿的麻醉管理情况,该婴儿被诊断为继发性PAP,并发严重肺炎和动脉导管未闭。患儿出现呼吸衰竭,需要进行WLL。采用的麻醉方法是静脉全身麻醉,气道管理采用在气管导管外放置BB以促进单肺通气(OLV)。该操作成功将血氧水平维持在90%以上,WLL顺利完成,未出现任何麻醉并发症。
本病例表明,气管插管联合在管腔外放置BB进行肺隔离是婴儿WLL的一种可行且有效的方法。