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Fiberoptic intubation through laryngeal mask airway for management of difficult airway in a child with Klippel–Feil syndrome
The ideal airway management modality in pediatric patients with syndromes like Klippel-Feil syndrome is a great challenge and is technically difficult for an anesthesiologist. Half of the patients present with the classic triad of short neck, low hairline, and fusion of cervical vertebra. Numerous a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141399/ https://www.ncbi.nlm.nih.gov/pubmed/25191201 http://dx.doi.org/10.4103/1658-354X.136637 |
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author | Bhat, Ravi Mane, Rajesh S. Patil, Manjunath C. Suresh, S. N. |
author_facet | Bhat, Ravi Mane, Rajesh S. Patil, Manjunath C. Suresh, S. N. |
author_sort | Bhat, Ravi |
collection | PubMed |
description | The ideal airway management modality in pediatric patients with syndromes like Klippel-Feil syndrome is a great challenge and is technically difficult for an anesthesiologist. Half of the patients present with the classic triad of short neck, low hairline, and fusion of cervical vertebra. Numerous associated anomalies like scoliosis or kyphosis, cleft palate, respiratory problems, deafness, genitourinary abnormalities, Sprengel's deformity (wherein the scapulae ride high on the back), synkinesia, cervical ribs, and congenital heart diseases may further add to the difficulty. Fiberoptic bronchoscopy alone can be technically difficult and patient cooperation also becomes very important, which is difficult in pediatric patients. Fiberoptic bronchoscopy with the aid of supraglottic airway devices is a viable alternative in the management of difficult airway in children. We report a case of Klippel-Feil syndrome in an 18-month-old girl posted for cleft palate surgery. Imaging of spine revealed complete fusion of the cervical vertebrae with hypoplastic C3 and C6 vertebrae and thoracic kyphosis. We successfully managed airway in this patient by fiberoptic intubation through classic laryngeal mask airway (LMA). After intubation, we used second smaller endotracheal tube (ETT) to stabilize and elongate the first ETT while removing the LMA. |
format | Online Article Text |
id | pubmed-4141399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41413992014-09-04 Fiberoptic intubation through laryngeal mask airway for management of difficult airway in a child with Klippel–Feil syndrome Bhat, Ravi Mane, Rajesh S. Patil, Manjunath C. Suresh, S. N. Saudi J Anaesth Case Report The ideal airway management modality in pediatric patients with syndromes like Klippel-Feil syndrome is a great challenge and is technically difficult for an anesthesiologist. Half of the patients present with the classic triad of short neck, low hairline, and fusion of cervical vertebra. Numerous associated anomalies like scoliosis or kyphosis, cleft palate, respiratory problems, deafness, genitourinary abnormalities, Sprengel's deformity (wherein the scapulae ride high on the back), synkinesia, cervical ribs, and congenital heart diseases may further add to the difficulty. Fiberoptic bronchoscopy alone can be technically difficult and patient cooperation also becomes very important, which is difficult in pediatric patients. Fiberoptic bronchoscopy with the aid of supraglottic airway devices is a viable alternative in the management of difficult airway in children. We report a case of Klippel-Feil syndrome in an 18-month-old girl posted for cleft palate surgery. Imaging of spine revealed complete fusion of the cervical vertebrae with hypoplastic C3 and C6 vertebrae and thoracic kyphosis. We successfully managed airway in this patient by fiberoptic intubation through classic laryngeal mask airway (LMA). After intubation, we used second smaller endotracheal tube (ETT) to stabilize and elongate the first ETT while removing the LMA. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4141399/ /pubmed/25191201 http://dx.doi.org/10.4103/1658-354X.136637 Text en Copyright: © Saudi Journal of Anaesthesia http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bhat, Ravi Mane, Rajesh S. Patil, Manjunath C. Suresh, S. N. Fiberoptic intubation through laryngeal mask airway for management of difficult airway in a child with Klippel–Feil syndrome |
title | Fiberoptic intubation through laryngeal mask airway for management of difficult airway in a child with Klippel–Feil syndrome |
title_full | Fiberoptic intubation through laryngeal mask airway for management of difficult airway in a child with Klippel–Feil syndrome |
title_fullStr | Fiberoptic intubation through laryngeal mask airway for management of difficult airway in a child with Klippel–Feil syndrome |
title_full_unstemmed | Fiberoptic intubation through laryngeal mask airway for management of difficult airway in a child with Klippel–Feil syndrome |
title_short | Fiberoptic intubation through laryngeal mask airway for management of difficult airway in a child with Klippel–Feil syndrome |
title_sort | fiberoptic intubation through laryngeal mask airway for management of difficult airway in a child with klippel–feil syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141399/ https://www.ncbi.nlm.nih.gov/pubmed/25191201 http://dx.doi.org/10.4103/1658-354X.136637 |
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