Malignant hyperthermia (MH) is a rare but fatal anaesthetic emergency. It is an autosomal dominant (AD) inherited disorder which is characterized by a hypermetabolic response of an individual upon exposure to a certain type of anaesthesia. We report a rare case of desflurane-induced MH in a Malay descent immediately following an uneventful exposure to sevoflurane. The administration of dantrolene in the immediate management successfully treated the patient.
CITATION STYLE
Lin, H. J., Halim, N. A., Joey, C., Ming, T. K., Katiman, F., Dintan, N. A., & Tat, Y. B. (2020). A rare occurrence of suspected delayed malignant hyperthermia in a young patient undergoing an orthopaedic surgery. Gazi Medical Journal, 31(4), 677–679. https://doi.org/10.12996/GMJ.2020.157
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