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Malignant Hyperthermia - StatPearls - NCBI Bookshelf
USA.gov. Malignant hyperthermia (MH) is a hereditary disorder of skeletal muscle that classically presents as a hypermetabolic response to halogenated anesthetic gasses and/or the depolarizing muscle relaxant succinylcholine.
Malignant hyperthermia: Diagnosis and management of acute ...
Malignant hyperthermia (MH) manifests clinically as a hypermetabolic crisis when an MH-susceptible (MHS) individual is exposed to a volatile anesthetic (eg, halothane, isoflurane, sevoflurane, desflurane) or succinylcholine [ 1-5 ]. This topic will discuss the incidence, pathophysiology, clinical manifestations, and acute management of MH.
Malignant hyperthermia - Wikipedia
Malignant hyperthermia ( MH) is a type of severe reaction that occurs in response to particular medications used during general anesthesia, among those who are susceptible. [1] Symptoms include muscle rigidity, fever, and a fast heart rate. [1] Complications can include muscle breakdown and high blood potassium.
Malignant Hyperthermia - Symptoms, Causes, Treatment | NORD
Disease Overview. Malignant hyperthermia (MH) is a dominantly inherited disorder of skeletal muscle that predisposes susceptible individuals to a life threatening adverse reaction (fulminant MH event) upon exposure to potent volatile anesthetics (halothane, isoflurane, sevoflurane, desflurane, etc.) and the skeletal muscle relaxant succinylcholine.
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