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成功对一名患有气管无名动脉瘘的马歇尔-史密斯综合征患者进行呼吸管理。

Successful respiratory management of a Marshall-Smith syndrome patient with a tracheo-innominate artery fistula.

作者信息

Noguchi Satoko, Saito Junichi, Kawaguchi Jun, Kushikata Tetsuya, Hirota Kazuyoshi

机构信息

Department of Anesthesiology, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki, Aomori, 036-8562, Japan.

出版信息

JA Clin Rep. 2020 May 22;6(1):37. doi: 10.1186/s40981-020-00343-6.

Abstract

BACKGROUND

Tracheo-innominate artery fistula (TIF) is a life-threatening complication of tracheostomy. We describe perioperative management for innominate artery transection in a case with TIF.

CASE PRESENTATION

A 4-year-old Japanese female with Marshal-Smith syndrome presented for management of TIF. She underwent tracheostomy at the age of 3 months and an uncuffed tracheostomy tube was inserted. One month before admission to our hospital, intermittent tracheal bleeding, suggesting TIF, occurred. Although we considered to change to a cuffed endotracheal tube, craniofacial abnormality suggested difficult oral intubation, and there was a possibility of rebleeding. Finally, innominate artery transection was performed under total intravenous anesthesia without changing the tracheostomy tube. Surgery completed uneventfully and she received mechanical ventilation under sedation for a day, followed by weaning without complications.

CONCLUSIONS

A cuffed tracheostomy tube should have been inserted before surgery for effective hemostasis against sudden bleeding from TIF even though conversion to oral intubation was difficult.

摘要

背景

气管无名动脉瘘(TIF)是气管切开术的一种危及生命的并发症。我们描述了一例TIF患者无名动脉横断的围手术期管理。

病例介绍

一名患有马歇尔-史密斯综合征的4岁日本女性因TIF前来治疗。她在3个月大时接受了气管切开术,并插入了无套囊气管切开管。入院前一个月,出现间歇性气管出血,提示TIF。尽管我们考虑更换为带套囊的气管内导管,但颅面异常提示经口插管困难,且有再次出血的可能。最后,在全静脉麻醉下进行无名动脉横断术,未更换气管切开管。手术顺利完成,她在镇静下接受了一天的机械通气,随后顺利脱机,无并发症。

结论

即使经口插管困难,术前也应插入带套囊的气管切开管,以有效止血,防止TIF突然出血。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0a9/7244681/5849d32c62f1/40981_2020_343_Fig1_HTML.jpg

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