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Erschienen in: Canadian Journal of Anesthesia/Journal canadien d'anesthésie 6/2018

29.03.2018 | Continuing Professional Development

Updated guide for the management of malignant hyperthermia

verfasst von: Sheila Riazi, MSc, MD, Natalia Kraeva, PhD, Philip M. Hopkins, MBBS, MD, FRCA

Erschienen in: Canadian Journal of Anesthesia/Journal canadien d'anesthésie | Ausgabe 6/2018

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Abstract

Purpose

This continuing professional development module aims to prepare anesthesiologists for the timely recognition and management of a malignant hyperthermia (MH) reaction, which is crucial for averting its life-threatening complications and ultimately for the patient’s survival.

Principal findings

Malignant hyperthermia is a genetic disorder of skeletal muscle cells affecting myoplasmic calcium homeostasis. It can present with nonspecific signs of a hypermetabolic reaction, which can be fatal if treatment, including administration of dantrolene sodium, is not implemented promptly. Rapid evaluation and rejection of alternative diagnoses can lead to a prompt diagnosis and treatment and therefore will significantly reduce the complications, including renal failure, cardiac dysfunction, disseminated intravascular coagulation, and death. After the reaction, patients should be observed for a minimum of 24 hr because of the possibility of recrudescence. As it is a genetic condition, survivors and their family members should be referred to a specialized MH centre for further testing and counselling.

Conclusions

The risk of dying from MH has increased over the past few years. A knowledgeable anesthesiologist who is diligent and attentive can recognize signs of an impending MH reaction and treat promptly to avoid complications of this deadly condition.
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Metadaten
Titel
Updated guide for the management of malignant hyperthermia
verfasst von
Sheila Riazi, MSc, MD
Natalia Kraeva, PhD
Philip M. Hopkins, MBBS, MD, FRCA
Publikationsdatum
29.03.2018
Verlag
Springer US
Erschienen in
Canadian Journal of Anesthesia/Journal canadien d'anesthésie / Ausgabe 6/2018
Print ISSN: 0832-610X
Elektronische ISSN: 1496-8975
DOI
https://doi.org/10.1007/s12630-018-1108-0

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