Malignant hyperthermia – state of knowledge

Malignant hyperthermia (MH) is a relatively rare, but potentially lethal genetic disorder. That disease is characterized by hypermetabolic response of the skeletal muscles caused by exposure to triggering agents e.g. volatile anesthetics or depolarizing neuromuscular blockers. The object of this...

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Main Authors: Michał Perszke, Dominika Egierska, Kamil Cieślak, Miłosz Berliński, Witold Świenc, Oskar Tokarczuk, Anna Walendzik
Format: Article
Language:English
Published: Kazimierz Wielki University 2022-09-01
Series:Journal of Education, Health and Sport
Subjects:
Online Access:https://apcz.umk.pl/JEHS/article/view/40023
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author Michał Perszke
Dominika Egierska
Kamil Cieślak
Miłosz Berliński
Witold Świenc
Oskar Tokarczuk
Anna Walendzik
author_facet Michał Perszke
Dominika Egierska
Kamil Cieślak
Miłosz Berliński
Witold Świenc
Oskar Tokarczuk
Anna Walendzik
author_sort Michał Perszke
collection DOAJ
description Malignant hyperthermia (MH) is a relatively rare, but potentially lethal genetic disorder. That disease is characterized by hypermetabolic response of the skeletal muscles caused by exposure to triggering agents e.g. volatile anesthetics or depolarizing neuromuscular blockers. The object of this article was to review and assess the most recent published works about the epidemiology, etiology, pathomechanism, therapy of the MH and the new advances in all these fields. Authors scrutinized PubMed and Google Scholar using keywords: malignant hyperthermia, volatile anesthetics, ryanodine receptor mutation. In addition to this, the references of chosen articles were manually scoured for supplementary applicable articles. The literature was selected on the basis of a general medicine readership and prioritized clinical practice guidelines, systematic reviews and case reports. The references include the latest reports on malignant hyperthermia, apart from works of historical importance. Available treatment methods consist mainly of pharmacotherapy, symptomatic treatment and monitoring of vital parameters. Dantrolene is a first-choice drug in initial treatment of MH and is considered the only specific antidote. In spite of the constant advances in the areas of medicine there is still much to be discovered about MH. Further studies are necessary, as the amount of credible evidence is not adequate.
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spelling doaj.art-7af115feb0974d799e3904f17e86fb9b2022-12-22T04:26:59ZengKazimierz Wielki UniversityJournal of Education, Health and Sport2391-83062022-09-0112910.12775/JEHS.2022.12.09.102Malignant hyperthermia – state of knowledgeMichał Perszke0Dominika Egierska1Kamil Cieślak2Miłosz Berliński3Witold Świenc4Oskar Tokarczuk5Anna Walendzik6Uniwersytet Medyczny im. Piastów Śląskich we WrocławiuUniwersytet Medyczny im. Piastów Śląskich we WrocławiuUniwersytet Medyczny im. Piastów Śląskich we WrocławiuUniwersytet Medyczny im. Piastów Śląskich we WrocławiuUniwersytet Medyczny im. Piastów Śląskich we WrocławiuUniwersytet Medyczny im. Piastów Śląskich we WrocławiuUniwersytet Medyczny im. Piastów Śląskich we Wrocławiu Malignant hyperthermia (MH) is a relatively rare, but potentially lethal genetic disorder. That disease is characterized by hypermetabolic response of the skeletal muscles caused by exposure to triggering agents e.g. volatile anesthetics or depolarizing neuromuscular blockers. The object of this article was to review and assess the most recent published works about the epidemiology, etiology, pathomechanism, therapy of the MH and the new advances in all these fields. Authors scrutinized PubMed and Google Scholar using keywords: malignant hyperthermia, volatile anesthetics, ryanodine receptor mutation. In addition to this, the references of chosen articles were manually scoured for supplementary applicable articles. The literature was selected on the basis of a general medicine readership and prioritized clinical practice guidelines, systematic reviews and case reports. The references include the latest reports on malignant hyperthermia, apart from works of historical importance. Available treatment methods consist mainly of pharmacotherapy, symptomatic treatment and monitoring of vital parameters. Dantrolene is a first-choice drug in initial treatment of MH and is considered the only specific antidote. In spite of the constant advances in the areas of medicine there is still much to be discovered about MH. Further studies are necessary, as the amount of credible evidence is not adequate. https://apcz.umk.pl/JEHS/article/view/40023malignant hyperthermiaryanodine receptorsuccinylocholineanesthetics
spellingShingle Michał Perszke
Dominika Egierska
Kamil Cieślak
Miłosz Berliński
Witold Świenc
Oskar Tokarczuk
Anna Walendzik
Malignant hyperthermia – state of knowledge
Journal of Education, Health and Sport
malignant hyperthermia
ryanodine receptor
succinylocholine
anesthetics
title Malignant hyperthermia – state of knowledge
title_full Malignant hyperthermia – state of knowledge
title_fullStr Malignant hyperthermia – state of knowledge
title_full_unstemmed Malignant hyperthermia – state of knowledge
title_short Malignant hyperthermia – state of knowledge
title_sort malignant hyperthermia state of knowledge
topic malignant hyperthermia
ryanodine receptor
succinylocholine
anesthetics
url https://apcz.umk.pl/JEHS/article/view/40023
work_keys_str_mv AT michałperszke malignanthyperthermiastateofknowledge
AT dominikaegierska malignanthyperthermiastateofknowledge
AT kamilcieslak malignanthyperthermiastateofknowledge
AT miłoszberlinski malignanthyperthermiastateofknowledge
AT witoldswienc malignanthyperthermiastateofknowledge
AT oskartokarczuk malignanthyperthermiastateofknowledge
AT annawalendzik malignanthyperthermiastateofknowledge