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Remimazolam in a Pediatric Patient With a Suspected Family History of Malignant Hyperthermia

Malignant hyperthermia (MH) is an acute hypermetabolic crisis, triggered in susceptible patients by the administration of succinylcholine or a volatile anesthetic agent. When providing anesthetic care for MH-susceptible patients, a total intravenous anesthetic technique with propofol or other sedati...

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Detalles Bibliográficos
Autores principales: Petkus, Holly, Willer, Brittany L., Tobias, Joseph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9451561/
https://www.ncbi.nlm.nih.gov/pubmed/36128061
http://dx.doi.org/10.14740/jmc3977
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author Petkus, Holly
Willer, Brittany L.
Tobias, Joseph D.
author_facet Petkus, Holly
Willer, Brittany L.
Tobias, Joseph D.
author_sort Petkus, Holly
collection PubMed
description Malignant hyperthermia (MH) is an acute hypermetabolic crisis, triggered in susceptible patients by the administration of succinylcholine or a volatile anesthetic agent. When providing anesthetic care for MH-susceptible patients, a total intravenous anesthetic technique with propofol or other sedative hypnotic is frequently chosen. Remimazolam is a novel benzodiazepine which, like midazolam, has sedative, anxiolytic, and amnestic properties. Ester metabolism results in a half-life of 5-10 min and a limited context sensitive half-life. We present anecdotal experience with its use as an adjunct to propofol anesthesia in a patient with a suspected family history of MH. Previous reports of the use of remimazolam in MH-susceptible patients are reviewed and its potential role in such patients discussed.
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spelling pubmed-94515612022-09-19 Remimazolam in a Pediatric Patient With a Suspected Family History of Malignant Hyperthermia Petkus, Holly Willer, Brittany L. Tobias, Joseph D. J Med Cases Case Report Malignant hyperthermia (MH) is an acute hypermetabolic crisis, triggered in susceptible patients by the administration of succinylcholine or a volatile anesthetic agent. When providing anesthetic care for MH-susceptible patients, a total intravenous anesthetic technique with propofol or other sedative hypnotic is frequently chosen. Remimazolam is a novel benzodiazepine which, like midazolam, has sedative, anxiolytic, and amnestic properties. Ester metabolism results in a half-life of 5-10 min and a limited context sensitive half-life. We present anecdotal experience with its use as an adjunct to propofol anesthesia in a patient with a suspected family history of MH. Previous reports of the use of remimazolam in MH-susceptible patients are reviewed and its potential role in such patients discussed. Elmer Press 2022-08 2022-08-19 /pmc/articles/PMC9451561/ /pubmed/36128061 http://dx.doi.org/10.14740/jmc3977 Text en Copyright 2022, Petkus et al. https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Petkus, Holly
Willer, Brittany L.
Tobias, Joseph D.
Remimazolam in a Pediatric Patient With a Suspected Family History of Malignant Hyperthermia
title Remimazolam in a Pediatric Patient With a Suspected Family History of Malignant Hyperthermia
title_full Remimazolam in a Pediatric Patient With a Suspected Family History of Malignant Hyperthermia
title_fullStr Remimazolam in a Pediatric Patient With a Suspected Family History of Malignant Hyperthermia
title_full_unstemmed Remimazolam in a Pediatric Patient With a Suspected Family History of Malignant Hyperthermia
title_short Remimazolam in a Pediatric Patient With a Suspected Family History of Malignant Hyperthermia
title_sort remimazolam in a pediatric patient with a suspected family history of malignant hyperthermia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9451561/
https://www.ncbi.nlm.nih.gov/pubmed/36128061
http://dx.doi.org/10.14740/jmc3977
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