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Successful respiratory management of a Marshall-Smith syndrome patient with a tracheo-innominate artery fistula
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 T...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244218/ https://www.ncbi.nlm.nih.gov/pubmed/32444904 http://dx.doi.org/10.1186/s40981-020-00343-6 |
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author | Noguchi, Satoko Saito, Junichi Kawaguchi, Jun Kushikata, Tetsuya Hirota, Kazuyoshi |
author_facet | Noguchi, Satoko Saito, Junichi Kawaguchi, Jun Kushikata, Tetsuya Hirota, Kazuyoshi |
author_sort | Noguchi, Satoko |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7244218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-72442182020-05-26 Successful respiratory management of a Marshall-Smith syndrome patient with a tracheo-innominate artery fistula Noguchi, Satoko Saito, Junichi Kawaguchi, Jun Kushikata, Tetsuya Hirota, Kazuyoshi JA Clin Rep Case Report 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. Springer Berlin Heidelberg 2020-05-22 /pmc/articles/PMC7244218/ /pubmed/32444904 http://dx.doi.org/10.1186/s40981-020-00343-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Case Report Noguchi, Satoko Saito, Junichi Kawaguchi, Jun Kushikata, Tetsuya Hirota, Kazuyoshi Successful respiratory management of a Marshall-Smith syndrome patient with a tracheo-innominate artery fistula |
title | Successful respiratory management of a Marshall-Smith syndrome patient with a tracheo-innominate artery fistula |
title_full | Successful respiratory management of a Marshall-Smith syndrome patient with a tracheo-innominate artery fistula |
title_fullStr | Successful respiratory management of a Marshall-Smith syndrome patient with a tracheo-innominate artery fistula |
title_full_unstemmed | Successful respiratory management of a Marshall-Smith syndrome patient with a tracheo-innominate artery fistula |
title_short | Successful respiratory management of a Marshall-Smith syndrome patient with a tracheo-innominate artery fistula |
title_sort | successful respiratory management of a marshall-smith syndrome patient with a tracheo-innominate artery fistula |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244218/ https://www.ncbi.nlm.nih.gov/pubmed/32444904 http://dx.doi.org/10.1186/s40981-020-00343-6 |
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