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Spinal anesthesia for muscle biopsy in an infant with a suspected neuromuscular disorder: a case report
BACKGROUND: Neuromuscular disorders (NMDs) occur in different forms and are generally diagnosed using muscle biopsy. Among the available anesthetic management options for infants with a suspected NMD are general anesthesia (GA) and regional anesthesia (RA), including spinal anesthesia (SA). Anesthes...
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/PMC7572997/ https://www.ncbi.nlm.nih.gov/pubmed/33078243 http://dx.doi.org/10.1186/s40981-020-00392-x |
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author | Ishida, Yoshiaki Morita, Masato Sasaki, Takahisa Taniguchi, Akiko |
author_facet | Ishida, Yoshiaki Morita, Masato Sasaki, Takahisa Taniguchi, Akiko |
author_sort | Ishida, Yoshiaki |
collection | PubMed |
description | BACKGROUND: Neuromuscular disorders (NMDs) occur in different forms and are generally diagnosed using muscle biopsy. Among the available anesthetic management options for infants with a suspected NMD are general anesthesia (GA) and regional anesthesia (RA), including spinal anesthesia (SA). Anesthesia selection is often challenging from the point of potential airway risks and anesthetic drug-related complications. CASE PRESENTATION: A 6-month-old male infant repeatedly underwent endotracheal intubation and extubation after birth because of respiratory muscle weakness and copious secretions. He was suspected of having NMD and was scheduled for muscle biopsy. His generalized hypotonia and decreased respiratory function presented a potentially difficult airway and complicated the selection of an appropriate anesthetic method. We selected SA and dexmedetomidine, which are safe for infants. CONCLUSION: We report the successful and effective anesthetic management of SA and dexmedetomidine in an infant with a suspected NMD. |
format | Online Article Text |
id | pubmed-7572997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-75729972020-10-20 Spinal anesthesia for muscle biopsy in an infant with a suspected neuromuscular disorder: a case report Ishida, Yoshiaki Morita, Masato Sasaki, Takahisa Taniguchi, Akiko JA Clin Rep Case Report BACKGROUND: Neuromuscular disorders (NMDs) occur in different forms and are generally diagnosed using muscle biopsy. Among the available anesthetic management options for infants with a suspected NMD are general anesthesia (GA) and regional anesthesia (RA), including spinal anesthesia (SA). Anesthesia selection is often challenging from the point of potential airway risks and anesthetic drug-related complications. CASE PRESENTATION: A 6-month-old male infant repeatedly underwent endotracheal intubation and extubation after birth because of respiratory muscle weakness and copious secretions. He was suspected of having NMD and was scheduled for muscle biopsy. His generalized hypotonia and decreased respiratory function presented a potentially difficult airway and complicated the selection of an appropriate anesthetic method. We selected SA and dexmedetomidine, which are safe for infants. CONCLUSION: We report the successful and effective anesthetic management of SA and dexmedetomidine in an infant with a suspected NMD. Springer Berlin Heidelberg 2020-10-19 /pmc/articles/PMC7572997/ /pubmed/33078243 http://dx.doi.org/10.1186/s40981-020-00392-x 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 Ishida, Yoshiaki Morita, Masato Sasaki, Takahisa Taniguchi, Akiko Spinal anesthesia for muscle biopsy in an infant with a suspected neuromuscular disorder: a case report |
title | Spinal anesthesia for muscle biopsy in an infant with a suspected neuromuscular disorder: a case report |
title_full | Spinal anesthesia for muscle biopsy in an infant with a suspected neuromuscular disorder: a case report |
title_fullStr | Spinal anesthesia for muscle biopsy in an infant with a suspected neuromuscular disorder: a case report |
title_full_unstemmed | Spinal anesthesia for muscle biopsy in an infant with a suspected neuromuscular disorder: a case report |
title_short | Spinal anesthesia for muscle biopsy in an infant with a suspected neuromuscular disorder: a case report |
title_sort | spinal anesthesia for muscle biopsy in an infant with a suspected neuromuscular disorder: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572997/ https://www.ncbi.nlm.nih.gov/pubmed/33078243 http://dx.doi.org/10.1186/s40981-020-00392-x |
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