A Proposed North American Approach for Genetic Testing of Individuals at Risk for Malignant Hyperthermia.
expert_opinion · Level V
Where this comes from
- Record sourced from PubMed, PMID 41805301.
- Also identified by DOI 10.1097/ALN.0000000000005849 and PMC identifier 12965816.
- Licence recorded as CC BY-NC-ND.
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Abstract
Malignant hyperthermia, a pharmacogenetic disorder of skeletal muscle, is a potentially fatal reaction triggered by exposure to volatile anesthetics or succinylcholine. Genetic testing of the three known involved genes (RYR1, CACNA1S, and STAC3) has become the first line of testing for malignant hyperthermia susceptibility. However, genetic testing has sensitivity of only up to 70%. Contracture testing may be used to rule out the disorder for some individuals. This study outlines a stepwise approach, using clinical history and assessment as well as interpretation of genetic variants to balance risks and benefits for individuals at risk of this disorder. This work has received an Affirmation of Value designation from the American Society of Anesthesiologists (Schaumburg, Illinois) and endorsement from the Canadian Anesthesiologists' Society (Toronto, Canada).
Medical subject headings
- Malignant Hyperthermia
- Genetic Testing