Clinical signs* |
Hypercarbia (elevated ETCO2) resistant to increases in minute ventilation |
Tachypnea or breathing over the ventilator |
Sinus tachycardia |
Masseter spasm with or without administration of succinylcholine |
Generalized muscle rigidity |
Peaked T waves or other arrhythmia (including PVCs, ventricular tachycardia or fibrillation) as a result of hyperkalemia |
Mixed acidosis on blood gas |
Hyperthermia |
Sweating |
Management |
Call for help and MH cart; for questions at any time call MH hotline: 1-800-644-9737 in US, 1-209-417-3722 outside US |
Discontinue inhaled anesthetics and succinylcholine; increase fresh gas flow to ≥ 10 L/minute, use non-triggering agents for remainder of procedure |
Notify surgeon; complete surgical procedure as quickly as possible |
Hyperventilate with 100% oxygen, perform endotracheal intubation if ETT not in place |
Insert carbon filters into breathing circuit after flushing the breathing circuit for ≥90 seconds at ≥10 L/minute fresh gas flow |
Administer dantrolene: |
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Send laboratory studies: venous or arterial blood gases, electrolytes, CK; repeat as necessary |
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Repeat after five minutes if ECG changes persist |
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Treat arrhythmias per ACLS, avoid calcium channel blockers; most arrhythmias respond to correction of hyperkalemia and acidosis |
Cool the patient as necessary: Start cooling for core temperature >39°C, discontinue cooling when temperature decreases to 38°C |
Insert Foley catheter, maintain urine output at 1 to 2 mL/kg/hour with IV fluid and diuretics |
Ongoing care |
Arrange ICU bed for at least 24 hours; monitor for recurrence, rhabdomyolysis, DIC |
After initial MH event is controlled, administer dantrolene 1 mg/kg IV every four to six hours or 0.25 mg/kg/hour for at least 24 hours |
ETCO2: end-tidal carbon dioxide; PVCs: premature ventricular contractions; MH: malignant hyperthermia; ETT: endotracheal tube; IV: intravenous; CK: creatine kinase; ECG: electrocardiogram; ACLS: advanced cardiac life support; ICU: intensive care unit; DIC: disseminated intravascular coagulation.
* The sequence and timing of the clinical manifestations of MH vary from patient to patient, and most patients do not develop all signs of MH.