Cargando…

A rare case of difficult airway management in a Klippel-Feil syndrome pediatric patient with osseous torticollis undergone orthopedic surgery: Difficult airway in pediatric patient with torticollis

BACKGROUND: Orthopedic surgery for cervical torticollis poses potential threat to airway management both in tracheal intubation and extubation. Klippel-Feil syndrome (KFS) is a complex syndrome of osseous and visceral anomalies. The anatomical characteristics of KFS might have significant implicatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Xiaoqing, Wang, Jun, Liu, Yajie, Li, Zhengqian, Han, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054383/
https://www.ncbi.nlm.nih.gov/pubmed/33874892
http://dx.doi.org/10.1186/s12871-021-01341-6
_version_ 1783680283917156352
author Zhang, Xiaoqing
Wang, Jun
Liu, Yajie
Li, Zhengqian
Han, Bin
author_facet Zhang, Xiaoqing
Wang, Jun
Liu, Yajie
Li, Zhengqian
Han, Bin
author_sort Zhang, Xiaoqing
collection PubMed
description BACKGROUND: Orthopedic surgery for cervical torticollis poses potential threat to airway management both in tracheal intubation and extubation. Klippel-Feil syndrome (KFS) is a complex syndrome of osseous and visceral anomalies. The anatomical characteristics of KFS might have significant implications for airway management. CASE PRESENTATION: This is a rare case of an 8-year-old boy presenting with osseous torticollis, congenital occipito-atlantal deformity, congenital basilar invagination and KFS undergone elective torticollis correction surgery. Though with difficulty, tracheal intubation was successfully performed. Extubation failed twice on postoperative day 2 and 10, and required tracheostomy. Based on radiological findings, we speculated that prolonged airway edema accounted for the main reason of the failed extubation, the hypertrophic tonsil and occipito-cervical fusion resulted in reduced oropharyngeal space and limited cervical range of motion. Moreover, the Chiari malformation and KFS complicated the airway condition and lead to prolonged airway obstruction. The tracheostomy casing was removed 1 month later. CONCLUSIONS: Cautions should be taken in extubation of pediatric patients undergone major osseous torticollis surgery. Reintubation should be prepared in case of failed extubation. Severe post-operative airway edema, complicated with hypertrophic tonsil, the structural abnormalities in the oropharyngeal cavity, and occipito-cervical deformities constituted the decreased oropharyngeal space and resulted in failed extubation. For severe airway compromise and prolonged intubation, tracheostomy should be considered.
format Online
Article
Text
id pubmed-8054383
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-80543832021-04-20 A rare case of difficult airway management in a Klippel-Feil syndrome pediatric patient with osseous torticollis undergone orthopedic surgery: Difficult airway in pediatric patient with torticollis Zhang, Xiaoqing Wang, Jun Liu, Yajie Li, Zhengqian Han, Bin BMC Anesthesiol Case Report BACKGROUND: Orthopedic surgery for cervical torticollis poses potential threat to airway management both in tracheal intubation and extubation. Klippel-Feil syndrome (KFS) is a complex syndrome of osseous and visceral anomalies. The anatomical characteristics of KFS might have significant implications for airway management. CASE PRESENTATION: This is a rare case of an 8-year-old boy presenting with osseous torticollis, congenital occipito-atlantal deformity, congenital basilar invagination and KFS undergone elective torticollis correction surgery. Though with difficulty, tracheal intubation was successfully performed. Extubation failed twice on postoperative day 2 and 10, and required tracheostomy. Based on radiological findings, we speculated that prolonged airway edema accounted for the main reason of the failed extubation, the hypertrophic tonsil and occipito-cervical fusion resulted in reduced oropharyngeal space and limited cervical range of motion. Moreover, the Chiari malformation and KFS complicated the airway condition and lead to prolonged airway obstruction. The tracheostomy casing was removed 1 month later. CONCLUSIONS: Cautions should be taken in extubation of pediatric patients undergone major osseous torticollis surgery. Reintubation should be prepared in case of failed extubation. Severe post-operative airway edema, complicated with hypertrophic tonsil, the structural abnormalities in the oropharyngeal cavity, and occipito-cervical deformities constituted the decreased oropharyngeal space and resulted in failed extubation. For severe airway compromise and prolonged intubation, tracheostomy should be considered. BioMed Central 2021-04-19 /pmc/articles/PMC8054383/ /pubmed/33874892 http://dx.doi.org/10.1186/s12871-021-01341-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Zhang, Xiaoqing
Wang, Jun
Liu, Yajie
Li, Zhengqian
Han, Bin
A rare case of difficult airway management in a Klippel-Feil syndrome pediatric patient with osseous torticollis undergone orthopedic surgery: Difficult airway in pediatric patient with torticollis
title A rare case of difficult airway management in a Klippel-Feil syndrome pediatric patient with osseous torticollis undergone orthopedic surgery: Difficult airway in pediatric patient with torticollis
title_full A rare case of difficult airway management in a Klippel-Feil syndrome pediatric patient with osseous torticollis undergone orthopedic surgery: Difficult airway in pediatric patient with torticollis
title_fullStr A rare case of difficult airway management in a Klippel-Feil syndrome pediatric patient with osseous torticollis undergone orthopedic surgery: Difficult airway in pediatric patient with torticollis
title_full_unstemmed A rare case of difficult airway management in a Klippel-Feil syndrome pediatric patient with osseous torticollis undergone orthopedic surgery: Difficult airway in pediatric patient with torticollis
title_short A rare case of difficult airway management in a Klippel-Feil syndrome pediatric patient with osseous torticollis undergone orthopedic surgery: Difficult airway in pediatric patient with torticollis
title_sort rare case of difficult airway management in a klippel-feil syndrome pediatric patient with osseous torticollis undergone orthopedic surgery: difficult airway in pediatric patient with torticollis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8054383/
https://www.ncbi.nlm.nih.gov/pubmed/33874892
http://dx.doi.org/10.1186/s12871-021-01341-6
work_keys_str_mv AT zhangxiaoqing ararecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis
AT wangjun ararecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis
AT liuyajie ararecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis
AT lizhengqian ararecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis
AT hanbin ararecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis
AT zhangxiaoqing rarecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis
AT wangjun rarecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis
AT liuyajie rarecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis
AT lizhengqian rarecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis
AT hanbin rarecaseofdifficultairwaymanagementinaklippelfeilsyndromepediatricpatientwithosseoustorticollisundergoneorthopedicsurgerydifficultairwayinpediatricpatientwithtorticollis