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Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: A case report
RATIONALE: Myotonic dystrophy is a progressive multisystem genetic heterogeneous disorder. General anesthesia with opioids increases the risk of prolonged postanesthetic respiratory recovery in myotonic dystrophy patients. PATIENT CONCERNS: A 20-year-old previously healthy woman was transferred to o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831368/ https://www.ncbi.nlm.nih.gov/pubmed/31027145 http://dx.doi.org/10.1097/MD.0000000000015427 |
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author | Ota, Koshi Nakamura, Yoshitsugu Nakamura, Eriko Takashima, Shogo Oka, Masahiro Ota, Kanna Sakaue, Masahide Sano, Yohei Takasu, Akira |
author_facet | Ota, Koshi Nakamura, Yoshitsugu Nakamura, Eriko Takashima, Shogo Oka, Masahiro Ota, Kanna Sakaue, Masahide Sano, Yohei Takasu, Akira |
author_sort | Ota, Koshi |
collection | PubMed |
description | RATIONALE: Myotonic dystrophy is a progressive multisystem genetic heterogeneous disorder. General anesthesia with opioids increases the risk of prolonged postanesthetic respiratory recovery in myotonic dystrophy patients. PATIENT CONCERNS: A 20-year-old previously healthy woman was transferred to our emergency department for further workup of respiratory failure, and massive ascites with abscess caused by endometriosis. Hypercapnic respiratory failure persisted under intensive care unit (ICU) management, but finally improved after cessation of fentanyl as a sedative agent. DIAGNOSIS: Myotonic dystrophy type 1. INTERVENTIONS: Massive ascites with abscess was accordingly managed by drainage, antibiotics, and an antifungal agent. Myotonic dystrophy type 1 was confirmed after molecular genetic testing revealed a cytosine-thymine-guanine repeat length of 400 to 450 in the DMPK gene. OUTCOMES: The patient was discharged without complications on hospital day 69. LESSONS: Myotonic dystrophy should be considered when hypercapnic respiratory failure persists in sedated ICU patients. Opioids should not be used for perioperative management of patients with myotonic dystrophy. |
format | Online Article Text |
id | pubmed-6831368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-68313682019-11-19 Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: A case report Ota, Koshi Nakamura, Yoshitsugu Nakamura, Eriko Takashima, Shogo Oka, Masahiro Ota, Kanna Sakaue, Masahide Sano, Yohei Takasu, Akira Medicine (Baltimore) 3900 RATIONALE: Myotonic dystrophy is a progressive multisystem genetic heterogeneous disorder. General anesthesia with opioids increases the risk of prolonged postanesthetic respiratory recovery in myotonic dystrophy patients. PATIENT CONCERNS: A 20-year-old previously healthy woman was transferred to our emergency department for further workup of respiratory failure, and massive ascites with abscess caused by endometriosis. Hypercapnic respiratory failure persisted under intensive care unit (ICU) management, but finally improved after cessation of fentanyl as a sedative agent. DIAGNOSIS: Myotonic dystrophy type 1. INTERVENTIONS: Massive ascites with abscess was accordingly managed by drainage, antibiotics, and an antifungal agent. Myotonic dystrophy type 1 was confirmed after molecular genetic testing revealed a cytosine-thymine-guanine repeat length of 400 to 450 in the DMPK gene. OUTCOMES: The patient was discharged without complications on hospital day 69. LESSONS: Myotonic dystrophy should be considered when hypercapnic respiratory failure persists in sedated ICU patients. Opioids should not be used for perioperative management of patients with myotonic dystrophy. Wolters Kluwer Health 2019-04-26 /pmc/articles/PMC6831368/ /pubmed/31027145 http://dx.doi.org/10.1097/MD.0000000000015427 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 3900 Ota, Koshi Nakamura, Yoshitsugu Nakamura, Eriko Takashima, Shogo Oka, Masahiro Ota, Kanna Sakaue, Masahide Sano, Yohei Takasu, Akira Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: A case report |
title | Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: A case report |
title_full | Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: A case report |
title_fullStr | Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: A case report |
title_full_unstemmed | Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: A case report |
title_short | Massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: A case report |
title_sort | massive abscess with prolonged respiratory failure due to newly diagnosed myotonic dystrophy: a case report |
topic | 3900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831368/ https://www.ncbi.nlm.nih.gov/pubmed/31027145 http://dx.doi.org/10.1097/MD.0000000000015427 |
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