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Accidental Ingestion of a NEO-fit Device Component by a Neonate
Background: Endotracheal tube securement devices are used to reduce the incidence of unplanned extubation of intubated patients. We describe the ingestion of part of an endotracheal tube securement device by a neonate to bring awareness of the risk of ingestion or aspiration of endotracheal tube sec...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Division of Ochsner Clinic Foundation
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477129/ https://www.ncbi.nlm.nih.gov/pubmed/36189090 http://dx.doi.org/10.31486/toj.21.0111 |
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author | Uwaifo, Omotola O. Abrigo, Ryan Jay |
author_facet | Uwaifo, Omotola O. Abrigo, Ryan Jay |
author_sort | Uwaifo, Omotola O. |
collection | PubMed |
description | Background: Endotracheal tube securement devices are used to reduce the incidence of unplanned extubation of intubated patients. We describe the ingestion of part of an endotracheal tube securement device by a neonate to bring awareness of the risk of ingestion or aspiration of endotracheal tube securement device components in this population. Case Report: A 13-day-old, former 31-week gestational age female infant was noted on routine radiologic evaluation to have a foreign body in the gastrointestinal tract. The foreign body was thought to be an artifact or an object overlying the radiologic image. However, review of previous imaging showed the object initially in the posterior pharynx with progressive migration into the gastrointestinal tract. The patient did not have any clinical features of gastrointestinal obstruction and had been tolerating enteral feeds. The infant's endotracheal tube securement had been changed from a NEO-fit device (CooperSurgical, Inc.) to a NeoBar device (Neotech Products) on day of life 5. The diagnosis of the foreign body was made 8 days later. The infant was followed with serial imaging per pediatric surgery recommendations. The foreign body was spontaneously passed via the rectum several days later without incident. Pathology identified the foreign body as a piece of the NEO-fit device. Conclusion: Awareness of the possibility of ingestion or aspiration from this endotracheal tube securement device is important for patient safety. |
format | Online Article Text |
id | pubmed-9477129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Academic Division of Ochsner Clinic Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-94771292022-09-29 Accidental Ingestion of a NEO-fit Device Component by a Neonate Uwaifo, Omotola O. Abrigo, Ryan Jay Ochsner J Case Reports and Clinical Observations Background: Endotracheal tube securement devices are used to reduce the incidence of unplanned extubation of intubated patients. We describe the ingestion of part of an endotracheal tube securement device by a neonate to bring awareness of the risk of ingestion or aspiration of endotracheal tube securement device components in this population. Case Report: A 13-day-old, former 31-week gestational age female infant was noted on routine radiologic evaluation to have a foreign body in the gastrointestinal tract. The foreign body was thought to be an artifact or an object overlying the radiologic image. However, review of previous imaging showed the object initially in the posterior pharynx with progressive migration into the gastrointestinal tract. The patient did not have any clinical features of gastrointestinal obstruction and had been tolerating enteral feeds. The infant's endotracheal tube securement had been changed from a NEO-fit device (CooperSurgical, Inc.) to a NeoBar device (Neotech Products) on day of life 5. The diagnosis of the foreign body was made 8 days later. The infant was followed with serial imaging per pediatric surgery recommendations. The foreign body was spontaneously passed via the rectum several days later without incident. Pathology identified the foreign body as a piece of the NEO-fit device. Conclusion: Awareness of the possibility of ingestion or aspiration from this endotracheal tube securement device is important for patient safety. Academic Division of Ochsner Clinic Foundation 2022 2022 /pmc/articles/PMC9477129/ /pubmed/36189090 http://dx.doi.org/10.31486/toj.21.0111 Text en ©2022 by the author(s); Creative Commons Attribution License (CC BY) https://creativecommons.org/licenses/by/4.0/©2022 by the author(s); licensee Ochsner Journal, Ochsner Clinic Foundation, New Orleans, LA. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (creativecommons.org/licenses/by/4.0/legalcode) that permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Case Reports and Clinical Observations Uwaifo, Omotola O. Abrigo, Ryan Jay Accidental Ingestion of a NEO-fit Device Component by a Neonate |
title | Accidental Ingestion of a NEO-fit Device Component by a Neonate |
title_full | Accidental Ingestion of a NEO-fit Device Component by a Neonate |
title_fullStr | Accidental Ingestion of a NEO-fit Device Component by a Neonate |
title_full_unstemmed | Accidental Ingestion of a NEO-fit Device Component by a Neonate |
title_short | Accidental Ingestion of a NEO-fit Device Component by a Neonate |
title_sort | accidental ingestion of a neo-fit device component by a neonate |
topic | Case Reports and Clinical Observations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477129/ https://www.ncbi.nlm.nih.gov/pubmed/36189090 http://dx.doi.org/10.31486/toj.21.0111 |
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