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Anesthetic management with a neuromuscular relaxant and sugammadex in a patient with Prader–Willi syndrome: A case report

Prader–Willi syndrome is a genetic disorder that is characterized by obesity, characteristic facial features, hypotonia, and sleep apnea. These abnormalities mean that airway management is difficult in such patients. Several previous reports suggest that neuromuscular blocking agents should not be u...

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Autores principales: Kim, Kyung Woo, Kim, Seung Hwan, Ahn, Eun Jin, Kim, Hyo Jin, Choi, Hey Ran, Bang, Si Ra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273580/
https://www.ncbi.nlm.nih.gov/pubmed/32547762
http://dx.doi.org/10.1177/2050313X20927616
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author Kim, Kyung Woo
Kim, Seung Hwan
Ahn, Eun Jin
Kim, Hyo Jin
Choi, Hey Ran
Bang, Si Ra
author_facet Kim, Kyung Woo
Kim, Seung Hwan
Ahn, Eun Jin
Kim, Hyo Jin
Choi, Hey Ran
Bang, Si Ra
author_sort Kim, Kyung Woo
collection PubMed
description Prader–Willi syndrome is a genetic disorder that is characterized by obesity, characteristic facial features, hypotonia, and sleep apnea. These abnormalities mean that airway management is difficult in such patients. Several previous reports suggest that neuromuscular blocking agents should not be used to reduce airway and respiratory complications in these patients. However, this is not always possible. Here, we report the case of a patient with Prader–Willi syndrome in whom anesthesia for ophthalmic surgery was managed successfully using sugammadex after administration of rocuronium.
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spelling pubmed-72735802020-06-15 Anesthetic management with a neuromuscular relaxant and sugammadex in a patient with Prader–Willi syndrome: A case report Kim, Kyung Woo Kim, Seung Hwan Ahn, Eun Jin Kim, Hyo Jin Choi, Hey Ran Bang, Si Ra SAGE Open Med Case Rep Case Report Prader–Willi syndrome is a genetic disorder that is characterized by obesity, characteristic facial features, hypotonia, and sleep apnea. These abnormalities mean that airway management is difficult in such patients. Several previous reports suggest that neuromuscular blocking agents should not be used to reduce airway and respiratory complications in these patients. However, this is not always possible. Here, we report the case of a patient with Prader–Willi syndrome in whom anesthesia for ophthalmic surgery was managed successfully using sugammadex after administration of rocuronium. SAGE Publications 2020-06-03 /pmc/articles/PMC7273580/ /pubmed/32547762 http://dx.doi.org/10.1177/2050313X20927616 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Kim, Kyung Woo
Kim, Seung Hwan
Ahn, Eun Jin
Kim, Hyo Jin
Choi, Hey Ran
Bang, Si Ra
Anesthetic management with a neuromuscular relaxant and sugammadex in a patient with Prader–Willi syndrome: A case report
title Anesthetic management with a neuromuscular relaxant and sugammadex in a patient with Prader–Willi syndrome: A case report
title_full Anesthetic management with a neuromuscular relaxant and sugammadex in a patient with Prader–Willi syndrome: A case report
title_fullStr Anesthetic management with a neuromuscular relaxant and sugammadex in a patient with Prader–Willi syndrome: A case report
title_full_unstemmed Anesthetic management with a neuromuscular relaxant and sugammadex in a patient with Prader–Willi syndrome: A case report
title_short Anesthetic management with a neuromuscular relaxant and sugammadex in a patient with Prader–Willi syndrome: A case report
title_sort anesthetic management with a neuromuscular relaxant and sugammadex in a patient with prader–willi syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273580/
https://www.ncbi.nlm.nih.gov/pubmed/32547762
http://dx.doi.org/10.1177/2050313X20927616
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