JA Clinical Reports (May 2020)

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

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

DOI
https://doi.org/10.1186/s40981-020-00343-6
Journal volume & issue
Vol. 6, no. 1
pp. 1 – 4

Abstract

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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.

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