Malignant hyperthermia is a rare but potentially fatal perioperative complication during cardiac surgery that requires prompt recognition and management with dantrolene.
Prompts inclusion of malignant hyperthermia in cardiac surgery differentials; leaves open optimal dantrolene protocols.
Malignant hyperthermia (MH) is a rare but potentially fatal disorder characterized by a hypermetabolic state produced by exposure to triggering agents such as volatile anesthetics and succinylcholine.1, 2 MH crises have also been recognized in the absence of exposure to obvious triggers. The incidence of MH may range from 1:5,000 to 1:100,000 anesthetic administrations, although the prevalence of predisposing genetic lesions is likely as common as 1 in every 3,000 individuals.1 Clinically, MH presents with a constellation of signs and symptoms including muscle rigidity, hypercarbia, tachycardia, acidosis, and hyperthermia, which if not promptly recognized and managed with dantrolene, is likely to lead to significant morbidity or death.
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Bloom et al. (2025) studied this question.
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