HYPERTHERMIA? Maintaining a normal body temperature through all phases of a surgical procedure is an essential component of patient safety and a critical responsibility for all members of the perioperative team.1 The normal range for a patient’s core body temperature, or normothermia, lies between 36° C and 38° C (96.8° F to 100.4° F).1 Under healthy conditions, this temperature is maintained through precise thermoregulatory mechanisms in the central nervous system, which balance heat production with heat loss.1 In a surgical setting, however, general, epidural, and other regional anesthetic agents as well as environmental factors can influence core body temperature, causing it to fall below or even exceed normal limits. Common temperature ranges are generally categorized as follows1: • Normothermia: 36° C to 38° C (96.8° F to 100.4° F) • Hypothermia: < 36° C (96.8° F) • Hyperthermia: > 38° C (100.4° F) An increase in core body temperature, or hyperthermia, can be classified as being either controlled or uncontrolled by the body. For instance, the onset of fever related to the presence of an infection is one example of controlled hyperthermia.2 Conversely, an increase in core temperature related to high ambient temperatures, exercise, or drug-induced impairment of the body’s thermoregulatory mechanisms would be considered uncontrolled hyperthermia.2 In the early 1960s, a condition known as malignant hyperthermia (MH) was first described.3,4 This form of uncontrolled hyperthermia is a potentially fatal hypermetabolic reaction to which certain individuals are genetically predisposed.5,6 In patients with this rare, autosomal dominant disorder, certain anesthetics, muscle relaxants, or extreme stress in the form of heat or exercise have the ability to trigger an MH crisis.4–6 Although rare, an MH crisis is a life-threatening event that can and does occur in the OR setting.5–7 If MH is not recognized and treated promptly, the patient may suffer severe adverse complications, such as cardiac arrest, organ failure, internal bleeding, brain damage, or even death.5–7 As a result, it is crucial that members of the perioperative team remain up- to-date on the signs and symptoms of MH, recommended patient interventions and drug therapies, and actions recommended to care for a patient experiencing an MH crisis. Teamwork, effective communication, and preparation are essential components in MH crisis training and can be life- saving for those patients who experience MH in the OR. MALIGNANT HYPERTHERMIA DISEASE STATE Overall, the incidence of diagnosed cases of anesthetic- induced MH crisis is approximately one in 15,000 children and one in 50,000 adults.6,8,9 However, as not all anesthetic- exposures may trigger a reaction in patients with MH, the potential susceptibility for an MH crisis has been estimated to be as high as one in every 200 patients.6,8 In the sections that follow, we will discuss the MH disease state in more detail, including: • Pathophysiology • Disease triggers • Risk factors • Diagnosis Pathophysiology Malignant hyperthermia is an autosomal dominant genetic mutation affecting the skeletal muscle.6 In normal skeletal muscle, the movement of calcium from the sarcoplasmic reticulum across the muscle cell membrane and into the myoplasm, or intracellular space, is a tightly regulated process that drives muscle contraction. Two receptors are integral to this process: the ryanodine receptor, which acts as the main calcium release channel, and the dihydropyridine receptor, which aids in initiating and terminating calcium release from the ryanodine receptor.6 Many patients with MH have been shown to have genetic mutations in the ryanodine or dihydropyridine receptors.6 As a result of this, when an MH crisis occurs, the regulation of 5